메뉴 건너뛰기




Volumn 116, Issue 15, 2016, Pages 8912-9000

Mn-, Fe-, and Co-Catalyzed Radical Hydrofunctionalizations of Olefins

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSIS; OLEFINS; REACTION KINETICS; SYNTHESIS (CHEMICAL);

EID: 84981724761     PISSN: 00092665     EISSN: 15206890     Source Type: Journal    
DOI: 10.1021/acs.chemrev.6b00334     Document Type: Review
Times cited : (759)

References (476)
  • 5
    • 84956919999 scopus 로고    scopus 로고
    • Markovnikov Free Radical Addition Reactions, a Sleeping Beauty Kissed to Life
    • Hoffmann, R. W. Markovnikov Free Radical Addition Reactions, a Sleeping Beauty Kissed to Life Chem. Soc. Rev. 2016, 45, 577-583 10.1039/C5CS00423C
    • (2016) Chem. Soc. Rev. , vol.45 , pp. 577-583
    • Hoffmann, R.W.1
  • 6
    • 85027942427 scopus 로고    scopus 로고
    • Fascinating Hydrogen Atom Transfer Chemistry of Alkenes Inspired by Problems in Total Synthesis
    • Simonneau, A.; Oestreich, M. Fascinating Hydrogen Atom Transfer Chemistry of Alkenes Inspired by Problems in Total Synthesis Angew. Chem., Int. Ed. 2015, 54, 3556-3558 10.1002/anie.201500557
    • (2015) Angew. Chem., Int. Ed. , vol.54 , pp. 3556-3558
    • Simonneau, A.1    Oestreich, M.2
  • 7
    • 84955181457 scopus 로고    scopus 로고
    • Metal-Catalyzed b-Functionalization of Michael Acceptors through Reductive Radical Addition Reactions
    • Streuff, J.; Gansäuer, A. Metal-Catalyzed b-Functionalization of Michael Acceptors through Reductive Radical Addition Reactions Angew. Chem., Int. Ed. 2015, 54, 14232-14242 10.1002/anie.201505231
    • (2015) Angew. Chem., Int. Ed. , vol.54 , pp. 14232-14242
    • Streuff, J.1    Gansäuer, A.2
  • 8
    • 0000902631 scopus 로고
    • Selectivity: A Key to Synthetic Efficiency
    • Trost, B. M. Selectivity: A Key to Synthetic Efficiency Science 1983, 219, 245-250 10.1126/science.219.4582.245
    • (1983) Science , vol.219 , pp. 245-250
    • Trost, B.M.1
  • 10
    • 0002197464 scopus 로고
    • On New Compounds of Carbon and Hydrogen, and on Certain Other Products Obtained during Decomposition of Oil by Heat
    • Faraday, M. On New Compounds of Carbon and Hydrogen, and on Certain Other Products Obtained during Decomposition of Oil by Heat Philos. Trans. R. Soc. 1825, 115, 440-466 10.1098/rstl.1825.0022
    • (1825) Philos. Trans. R. Soc. , vol.115 , pp. 440-466
    • Faraday, M.1
  • 11
    • 84886983840 scopus 로고
    • On the Mutual Action of Sulphuric Acid and Alcohol, and on the Nature of the Process by which Ether is Formed
    • Hennell, H. On the Mutual Action of Sulphuric Acid and Alcohol, and on the Nature of the Process by which Ether is Formed Philos. Trans. R. Soc. 1828, 118, 365-371 10.1098/rstl.1828.0021
    • (1828) Philos. Trans. R. Soc. , vol.118 , pp. 365-371
    • Hennell, H.1
  • 12
    • 0029982116 scopus 로고    scopus 로고
    • Mechanism of Nucleophilic Substitution and Elimination Reactions at Tertiary Carbon in Largely Aqueous Solutions: Lifetime of a Simple Tertiary Carbocation
    • Toteva, M. M.; Richard, J. P. Mechanism of Nucleophilic Substitution and Elimination Reactions at Tertiary Carbon in Largely Aqueous Solutions: Lifetime of a Simple Tertiary Carbocation J. Am. Chem. Soc. 1996, 118, 11434-11445 10.1021/ja9617451
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 11434-11445
    • Toteva, M.M.1    Richard, J.P.2
  • 13
    • 17144408314 scopus 로고    scopus 로고
    • Carborane Acids. New Strong Yet Gentle'' Acids for Organic and Inorganic Chemistry
    • Reed, C. A. Carborane Acids. New Strong Yet Gentle'' Acids for Organic and Inorganic Chemistry Chem. Commun. 2005, 1669-1677 10.1039/B415425H
    • (2005) Chem. Commun. , pp. 1669-1677
    • Reed, C.A.1
  • 14
    • 0001728539 scopus 로고
    • Formation of CC Bonds by Addition of Free Radicals to Alkenes
    • Giese, B. Formation of CC Bonds by Addition of Free Radicals to Alkenes Angew. Chem., Int. Ed. Engl. 1983, 22, 753-764 10.1002/anie.198307531
    • (1983) Angew. Chem., Int. Ed. Engl. , vol.22 , pp. 753-764
    • Giese, B.1
  • 15
    • 0000886120 scopus 로고
    • Copolymerization. II. The Copolymerization of Acrylonitrile, Methyl Methacrylate, Styrene and Vinylidene Chloride
    • Lewis, F. M.; Mayo, F. R.; Hulse, W. F. Copolymerization. II. The Copolymerization of Acrylonitrile, Methyl Methacrylate, Styrene and Vinylidene Chloride J. Am. Chem. Soc. 1945, 67, 1701-1705 10.1021/ja01226a025
    • (1945) J. Am. Chem. Soc. , vol.67 , pp. 1701-1705
    • Lewis, F.M.1    Mayo, F.R.2    Hulse, W.F.3
  • 16
    • 0000390580 scopus 로고
    • Group Transfer Addition Reactions of Methyl(phenylseleno)malononitrile to Alkenes
    • Curran, D. P.; Eichenberger, E.; Collis, M.; Roepel, M. G.; Thoma, G. Group Transfer Addition Reactions of Methyl(phenylseleno)malononitrile to Alkenes J. Am. Chem. Soc. 1994, 116, 4279-4288 10.1021/ja00089a017
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 4279-4288
    • Curran, D.P.1    Eichenberger, E.2    Collis, M.3    Roepel, M.G.4    Thoma, G.5
  • 17
    • 84985325717 scopus 로고
    • Separation of Polar and Steric Effects on Absolute Rate Constants and Arrhenius Parameters for the Reaction of tert-Butyl Radicals with Alkenes
    • Munger, K.; Fischer, H. Separation of Polar and Steric Effects on Absolute Rate Constants and Arrhenius Parameters for the Reaction of tert-Butyl Radicals with Alkenes Int. J. Chem. Kinet. 1985, 17, 809-829 10.1002/kin.550170803
    • (1985) Int. J. Chem. Kinet. , vol.17 , pp. 809-829
    • Munger, K.1    Fischer, H.2
  • 18
    • 0033484573 scopus 로고    scopus 로고
    • Polarity-Reversal Catalysis of Hydrogen-Atom Abstraction Reactions: Concepts and Applications in Organic Chemistry
    • Roberts, B. P. Polarity-Reversal Catalysis of Hydrogen-Atom Abstraction Reactions: Concepts and Applications in Organic Chemistry Chem. Soc. Rev. 1999, 28, 25-35 10.1039/a804291h
    • (1999) Chem. Soc. Rev. , vol.28 , pp. 25-35
    • Roberts, B.P.1
  • 19
    • 84981704776 scopus 로고    scopus 로고
    • An Organizational Format for the Classification of Functional Groups. Application to the Construction of Difunctional Relationships. Chemistry 206: Advanced Organic Chemistry, Handout 27A; Harvard University
    • Evans, D. A. An Organizational Format for the Classification of Functional Groups. Application to the Construction of Difunctional Relationships. Chemistry 206: Advanced Organic Chemistry, Handout 27A; Harvard University, 2001.
    • (2001)
    • Evans, D.A.1
  • 20
    • 84893467790 scopus 로고    scopus 로고
    • A Practical and Catalytic Reductive Olefin Coupling
    • Lo, J. C.; Yabe, Y.; Baran, P. S. A Practical and Catalytic Reductive Olefin Coupling J. Am. Chem. Soc. 2014, 136, 1304-1307 10.1021/ja4117632
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 1304-1307
    • Lo, J.C.1    Yabe, Y.2    Baran, P.S.3
  • 21
    • 84922792786 scopus 로고    scopus 로고
    • Functionalized Olefin Cross-Coupling to Construct Carbon-Carbon Bonds
    • Lo, J. C.; Gui, J.; Yabe, Y.; Pan, C.-M.; Baran, P. S. Functionalized Olefin Cross-Coupling to Construct Carbon-Carbon Bonds Nature 2014, 516, 343-348 10.1038/nature14006
    • (2014) Nature , vol.516 , pp. 343-348
    • Lo, J.C.1    Gui, J.2    Yabe, Y.3    Pan, C.-M.4    Baran, P.S.5
  • 22
    • 34250772270 scopus 로고    scopus 로고
    • Mild Cobalt-Catalyzed Hydrocyanation of Olefins with Tosyl Cyanide
    • Gaspar, B.; Carreira, E. M. Mild Cobalt-Catalyzed Hydrocyanation of Olefins with Tosyl Cyanide Angew. Chem., Int. Ed. 2007, 46, 4519-4522 10.1002/anie.200700575
    • (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 4519-4522
    • Gaspar, B.1    Carreira, E.M.2
  • 23
    • 70349377159 scopus 로고    scopus 로고
    • Cobalt Catalyzed Functionalization of Unactivated Alkenes: Regioselective Reductive C-C Bond Forming Reactions
    • Gaspar, B.; Carreira, E. M. Cobalt Catalyzed Functionalization of Unactivated Alkenes: Regioselective Reductive C-C Bond Forming Reactions J. Am. Chem. Soc. 2009, 131, 13214-13215 10.1021/ja904856k
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 13214-13215
    • Gaspar, B.1    Carreira, E.M.2
  • 24
    • 84893442643 scopus 로고    scopus 로고
    • Simple, Chemoselective Hydrogenation with Thermodynamic Stereocontrol
    • Iwasaki, K.; Wan, K. K.; Oppedisano, A.; Crossley, S. W. M.; Shenvi, R. A. Simple, Chemoselective Hydrogenation with Thermodynamic Stereocontrol J. Am. Chem. Soc. 2014, 136, 1300-1303 10.1021/ja412342g
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 1300-1303
    • Iwasaki, K.1    Wan, K.K.2    Oppedisano, A.3    Crossley, S.W.M.4    Shenvi, R.A.5
  • 25
    • 84925438133 scopus 로고    scopus 로고
    • Total Synthesis of Vinblastine, Related Natural Products, and Key Analogues and Development of Inspired Methodology Suitable for the Systematic Study of Their Structure-Function Properties
    • Sears, J. E.; Boger, D. L. Total Synthesis of Vinblastine, Related Natural Products, and Key Analogues and Development of Inspired Methodology Suitable for the Systematic Study of Their Structure-Function Properties Acc. Chem. Res. 2015, 48, 653-662 10.1021/ar500400w
    • (2015) Acc. Chem. Res. , vol.48 , pp. 653-662
    • Sears, J.E.1    Boger, D.L.2
  • 26
    • 67949110944 scopus 로고    scopus 로고
    • Total Synthesis of Vinblastine, Vincristine, Related Natural Products, and Key Structural Analogues
    • Ishikawa, H.; Colby, D. A.; Seto, S.; Va, P.; Tam, A.; Kakei, H.; Rayl, T. J.; Hwang, I.; Boger, D. L. Total Synthesis of Vinblastine, Vincristine, Related Natural Products, and Key Structural Analogues J. Am. Chem. Soc. 2009, 131, 4904-4916 10.1021/ja809842b
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 4904-4916
    • Ishikawa, H.1    Colby, D.A.2    Seto, S.3    Va, P.4    Tam, A.5    Kakei, H.6    Rayl, T.J.7    Hwang, I.8    Boger, D.L.9
  • 27
    • 84900827256 scopus 로고    scopus 로고
    • A Method for the Selective Hydrogenation of Alkenyl Halides to Alkyl Halides
    • King, S. M.; Ma, X.; Herzon, S. B. A Method for the Selective Hydrogenation of Alkenyl Halides to Alkyl Halides J. Am. Chem. Soc. 2014, 136, 6884-6887 10.1021/ja502885c
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 6884-6887
    • King, S.M.1    Ma, X.2    Herzon, S.B.3
  • 28
    • 84915820390 scopus 로고    scopus 로고
    • Simple, Chemoselective, Catalytic Olefin Isomerization
    • Crossley, S. W. M.; Barabé, F.; Shenvi, R. A. Simple, Chemoselective, Catalytic Olefin Isomerization J. Am. Chem. Soc. 2014, 136, 16788-16791 10.1021/ja5105602
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 16788-16791
    • Crossley, S.W.M.1    Barabé, F.2    Shenvi, R.A.3
  • 30
    • 0035780989 scopus 로고    scopus 로고
    • Catalytic Chain Transfer in Free-Radical Polymerizations
    • Gridnev, A. A.; Ittel, S. D. Catalytic Chain Transfer in Free-Radical Polymerizations Chem. Rev. 2001, 101, 3611-3660 10.1021/cr9901236
    • (2001) Chem. Rev. , vol.101 , pp. 3611-3660
    • Gridnev, A.A.1    Ittel, S.D.2
  • 31
    • 84940702815 scopus 로고    scopus 로고
    • Manganese Organometallic Compounds in Homogeneous Catalysis: Past, Present, and Prospects
    • Valyaev, D. A.; Lavigne, G.; Lugan, N. Manganese Organometallic Compounds in Homogeneous Catalysis: Past, Present, and Prospects Coord. Chem. Rev. 2016, 308, 191-235 10.1016/j.ccr.2015.06.015
    • (2016) Coord. Chem. Rev. , vol.308 , pp. 191-235
    • Valyaev, D.A.1    Lavigne, G.2    Lugan, N.3
  • 32
    • 84929359098 scopus 로고    scopus 로고
    • Iron Catalysis in Organic Synthesis
    • Bauer, I.; Knölker, H.-J. Iron Catalysis in Organic Synthesis Chem. Rev. 2015, 115, 3170-3387 10.1021/cr500425u
    • (2015) Chem. Rev. , vol.115 , pp. 3170-3387
    • Bauer, I.1    Knölker, H.-J.2
  • 33
    • 84920772634 scopus 로고    scopus 로고
    • Iron-Catalysed Hydrofunctionalisation of Alkenes and Alkynes
    • Greenhalgh, M. D.; Jones, A. S.; Thomas, S. P. Iron-Catalysed Hydrofunctionalisation of Alkenes and Alkynes ChemCatChem 2015, 7, 190-222 10.1002/cctc.201402693
    • (2015) ChemCatChem , vol.7 , pp. 190-222
    • Greenhalgh, M.D.1    Jones, A.S.2    Thomas, S.P.3
  • 34
    • 0036006066 scopus 로고    scopus 로고
    • The Use of Free Radical Initiators Bearing Metal-Metal, Metal-Hydrogen and Non-Metal-Hydrogen Bonds in Synthesis
    • Gilbert, B. C.; Parsons, A. F. The Use of Free Radical Initiators Bearing Metal-Metal, Metal-Hydrogen and Non-Metal-Hydrogen Bonds in Synthesis J. Chem. Soc., Perkin Trans. 2 2002, 367-387 10.1039/b102044g
    • (2002) J. Chem. Soc., Perkin Trans. 2 , pp. 367-387
    • Gilbert, B.C.1    Parsons, A.F.2
  • 35
    • 84981723043 scopus 로고    scopus 로고
    • Main Group Lewis Acid-Mediated Transformations of Transition-Metal Hydride Complexes
    • Maity, A.; Teets, T. S. Main Group Lewis Acid-Mediated Transformations of Transition-Metal Hydride Complexes Chem. Rev. 2016, 10.1021/acs.chemrev.6b00034
    • (2016) Chem. Rev.
    • Maity, A.1    Teets, T.S.2
  • 36
    • 0000722861 scopus 로고
    • Determination and Significance of Transition Metal-Alkyl Bond Dissociation Energies
    • Halpern, J. Determination and Significance of Transition Metal-Alkyl Bond Dissociation Energies Acc. Chem. Res. 1982, 15, 238-244 10.1021/ar00080a002
    • (1982) Acc. Chem. Res. , vol.15 , pp. 238-244
    • Halpern, J.1
  • 37
    • 0022047222 scopus 로고
    • Free Radical Mechanisms in Organometallic and Bioorganometallic Chemistry
    • Halpern, J. Free Radical Mechanisms in Organometallic and Bioorganometallic Chemistry Pure Appl. Chem. 1986, 58, 575-584 10.1351/pac198658040575
    • (1986) Pure Appl. Chem. , vol.58 , pp. 575-584
    • Halpern, J.1
  • 38
    • 0002993450 scopus 로고
    • Recent Advances in Aerobic Oxygenation
    • Mukaiyama, T.; Yamada, T. Recent Advances in Aerobic Oxygenation Bull. Chem. Soc. Jpn. 1995, 68, 17-35 10.1246/bcsj.68.17
    • (1995) Bull. Chem. Soc. Jpn. , vol.68 , pp. 17-35
    • Mukaiyama, T.1    Yamada, T.2
  • 39
    • 0015385044 scopus 로고
    • Enzymatic Hydroxylations with Molecular Oxygen
    • Ullrich, V. Enzymatic Hydroxylations with Molecular Oxygen Angew. Chem., Int. Ed. Engl. 1972, 11, 701-712 10.1002/anie.197207011
    • (1972) Angew. Chem., Int. Ed. Engl. , vol.11 , pp. 701-712
    • Ullrich, V.1
  • 40
    • 0000513113 scopus 로고
    • Bio-Mimetic Oxygenation
    • Matsuura, T. Bio-Mimetic Oxygenation Tetrahedron 1977, 33, 2869-2905 10.1016/0040-4020(77)88020-4
    • (1977) Tetrahedron , vol.33 , pp. 2869-2905
    • Matsuura, T.1
  • 41
    • 0018943782 scopus 로고
    • The Role of Peroxymetallation in Selective Oxidative Processes
    • Mimoun, H. The Role of Peroxymetallation in Selective Oxidative Processes J. Mol. Catal. 1980, 7, 1-29 10.1016/0304-5102(80)85001-2
    • (1980) J. Mol. Catal. , vol.7 , pp. 1-29
    • Mimoun, H.1
  • 42
    • 0023367217 scopus 로고
    • Cytochrome P-450 and synthetic models
    • Mansuy, D. Cytochrome P-450 and synthetic models Pure Appl. Chem. 1987, 59, 759-770 10.1351/pac198759060759
    • (1987) Pure Appl. Chem. , vol.59 , pp. 759-770
    • Mansuy, D.1
  • 43
    • 21944440277 scopus 로고    scopus 로고
    • Recent Advances in Transition Metal Catalyzed Oxidation of Organic Substrates with Molecular Oxygen
    • Punniyamurthy, T.; Velusamy, S.; Iqbal, J. Recent Advances in Transition Metal Catalyzed Oxidation of Organic Substrates with Molecular Oxygen Chem. Rev. 2005, 105, 2329-2364 10.1021/cr050523v
    • (2005) Chem. Rev. , vol.105 , pp. 2329-2364
    • Punniyamurthy, T.1    Velusamy, S.2    Iqbal, J.3
  • 44
    • 18544384019 scopus 로고
    • Oxidation of Tartaric Acid in Presence of Iron
    • Fenton, H. J. H. Oxidation of Tartaric Acid in Presence of Iron J. Chem. Soc., Trans. 1894, 65, 899-910 10.1039/CT8946500899
    • (1894) J. Chem. Soc., Trans. , vol.65 , pp. 899-910
    • Fenton, H.J.H.1
  • 45
    • 84929017892 scopus 로고    scopus 로고
    • - Substrates: Are •oH Radicals Formed in the Process?
    • - Substrates: are •OH Radicals Formed in the Process? J. Phys. Chem. A 2015, 119, 4200-4206 10.1021/jp512826f
    • (2015) J. Phys. Chem. A , vol.119 , pp. 4200-4206
    • Kornweitz, H.1    Burg, A.2    Meyerstein, D.3
  • 46
    • 0007506829 scopus 로고
    • Free Radical Mechanisms in Autooxidation Processes
    • Simic, M. G. Free Radical Mechanisms in Autooxidation Processes J. Chem. Educ. 1981, 58, 125-131 10.1021/ed058p125
    • (1981) J. Chem. Educ. , vol.58 , pp. 125-131
    • Simic, M.G.1
  • 47
    • 0016313337 scopus 로고
    • Oxidation of Olefins in the Presence of Transition Metal Complexes
    • Lyons, J. E. Oxidation of Olefins in the Presence of Transition Metal Complexes Adv. Chem. Ser. 1974, 132, 64-89 10.1021/ba-1974-0132.ch006
    • (1974) Adv. Chem. Ser. , vol.132 , pp. 64-89
    • Lyons, J.E.1
  • 51
    • 50449100139 scopus 로고
    • The Carbon Monoxide-Binding Pigment of Liver Microsomes: II. Solubilization, Purification, and Properties
    • Omura, T.; Sato, R. The Carbon Monoxide-Binding Pigment of Liver Microsomes: II. Solubilization, Purification, and Properties J. Biol. Chem. 1964, 239, 2379-2385
    • (1964) J. Biol. Chem. , vol.239 , pp. 2379-2385
    • Omura, T.1    Sato, R.2
  • 52
    • 0000507208 scopus 로고
    • P-450 Type Oxygen Activation by Porphyrin-Manganese Complex
    • Tabushi, I.; Koga, N. P-450 Type Oxygen Activation by Porphyrin-Manganese Complex J. Am. Chem. Soc. 1979, 101, 6456-6458 10.1021/ja00515a063
    • (1979) J. Am. Chem. Soc. , vol.101 , pp. 6456-6458
    • Tabushi, I.1    Koga, N.2
  • 53
    • 0001202995 scopus 로고
    • Pigments of Rat Liver Microsomes
    • Klingenberg, M. Pigments of Rat Liver Microsomes Arch. Biochem. Biophys. 1958, 75, 376-386 10.1016/0003-9861(58)90436-3
    • (1958) Arch. Biochem. Biophys. , vol.75 , pp. 376-386
    • Klingenberg, M.1
  • 54
    • 0001325090 scopus 로고
    • Manganese Phthalocyanine as a Model of Tryptophan-2,3-Dioxygenase
    • Uchida, K.; Soma, M.; Naito, S.; Onishi, T.; Tamaru, K. Manganese Phthalocyanine as a Model of Tryptophan-2,3-Dioxygenase Chem. Lett. 1978, 7, 471-474 10.1246/cl.1978.471
    • (1978) Chem. Lett. , vol.7 , pp. 471-474
    • Uchida, K.1    Soma, M.2    Naito, S.3    Onishi, T.4    Tamaru, K.5
  • 56
    • 3543049653 scopus 로고
    • Reaction of Indoles with Molecular Oxygen Catalyzed by Metalloporphyrins
    • Dufour, M. N.; Crumbliss, A. L.; Johnston, G.; Gaudemer, A. Reaction of Indoles with Molecular Oxygen Catalyzed by Metalloporphyrins J. Mol. Catal. 1980, 7, 277-287 10.1016/0304-5102(80)85025-5
    • (1980) J. Mol. Catal. , vol.7 , pp. 277-287
    • Dufour, M.N.1    Crumbliss, A.L.2    Johnston, G.3    Gaudemer, A.4
  • 57
    • 37049093764 scopus 로고
    • Manganese Porphyrin-Catalysed Oxidation of Olefins to Ketones by Molecular Oxygen
    • Perree-Fauvet, M.; Gaudemer, A. Manganese Porphyrin-Catalysed Oxidation of Olefins to Ketones by Molecular Oxygen J. Chem. Soc., Chem. Commun. 1981, 874-875 10.1039/C39810000874
    • (1981) J. Chem. Soc., Chem. Commun. , pp. 874-875
    • Perree-Fauvet, M.1    Gaudemer, A.2
  • 58
  • 59
    • 0024715825 scopus 로고
    • Aromatic Olefin Oxygenation with Tetrahydroborate and Dioxygen Catalyzed by a Manganese Porphyrin
    • Shimizu, M.; Orita, H.; Hayakawa, T.; Takehira, K. Aromatic Olefin Oxygenation with Tetrahydroborate and Dioxygen Catalyzed by a Manganese Porphyrin J. Mol. Catal. 1989, 53, 165-172 10.1016/0304-5102(89)85001-1
    • (1989) J. Mol. Catal. , vol.53 , pp. 165-172
    • Shimizu, M.1    Orita, H.2    Hayakawa, T.3    Takehira, K.4
  • 60
    • 0025491743 scopus 로고
    • Biomimetic Models of Cytochrome P-450 Monooxygenases: Studies on Cyclohexene Oxygenation in Metalloporphyrin-Sodium Borohydride-Microcrystalline Cellulose-Oxygen Systems
    • Nishiki, M.; Satoh, T.; Sakurai, H. Biomimetic Models of Cytochrome P-450 Monooxygenases: Studies on Cyclohexene Oxygenation in Metalloporphyrin-Sodium Borohydride-Microcrystalline Cellulose-Oxygen Systems J. Mol. Catal. 1990, 62, 79-91 10.1016/0304-5102(90)85242-A
    • (1990) J. Mol. Catal. , vol.62 , pp. 79-91
    • Nishiki, M.1    Satoh, T.2    Sakurai, H.3
  • 61
    • 0001441516 scopus 로고
    • Mechanisms for (Porphinato)manganese(III)-Catalyzed Oxygenation and Reduction of Styrenes in Benzene-Ethanol Containing Sodium Borohydride
    • Takeuchi, M.; Kano, K. Mechanisms for (Porphinato)manganese(III)-Catalyzed Oxygenation and Reduction of Styrenes in Benzene-Ethanol Containing Sodium Borohydride Bull. Chem. Soc. Jpn. 1994, 67, 1726-1733 10.1246/bcsj.67.1726
    • (1994) Bull. Chem. Soc. Jpn. , vol.67 , pp. 1726-1733
    • Takeuchi, M.1    Kano, K.2
  • 62
    • 0022056782 scopus 로고
    • Oxygen Activation and Olefin Oxygenation by Iron(III) porphyrin as a Model of Cytochrome P-450
    • Santa, T.; Mori, T.; Hirobe, M. Oxygen Activation and Olefin Oxygenation by Iron(III) porphyrin as a Model of Cytochrome P-450 Chem. Pharm. Bull. 1985, 33, 2175-2178 10.1248/cpb.33.2175
    • (1985) Chem. Pharm. Bull. , vol.33 , pp. 2175-2178
    • Santa, T.1    Mori, T.2    Hirobe, M.3
  • 63
    • 0003148020 scopus 로고
    • Porphinatoiron-Catalyzed Oxygenation of Styrene in Aqueous Solution
    • Kano, K.; Takagi, H.; Takeuchi, M.; Hashimoto, S.; Yoshida, Z.-i. Porphinatoiron-Catalyzed Oxygenation of Styrene in Aqueous Solution Chem. Lett. 1991, 20, 519-522 10.1246/cl.1991.519
    • (1991) Chem. Lett. , vol.20 , pp. 519-522
    • Kano, K.1    Takagi, H.2    Takeuchi, M.3    Hashimoto, S.4    Yoshida, Z.-I.5
  • 64
    • 0011366516 scopus 로고
    • (s-Alkyl)iron Complexes as Intermediates in (Porphinato)Iron-Mediated Reduction of Alkenes and Alkynes with Sodium Borohydride
    • Takeuchi, M.; Kano, K. (s-Alkyl)iron Complexes as Intermediates in (Porphinato)Iron-Mediated Reduction of Alkenes and Alkynes with Sodium Borohydride Organometallics 1993, 12, 2059-2064 10.1021/om00030a015
    • (1993) Organometallics , vol.12 , pp. 2059-2064
    • Takeuchi, M.1    Kano, K.2
  • 66
    • 3042990330 scopus 로고
    • 4 in the Presence of Alkenes. Formation of Organoiron(III) Porphyrins
    • 4 in the Presence of Alkenes. Formation of Organoiron(III) Porphyrins Chem. Lett. 1992, 21, 377-380 10.1246/cl.1992.377
    • (1992) Chem. Lett. , vol.21 , pp. 377-380
    • Setsune, J.-I.1    Ishimaru, Y.2    Sera, A.3
  • 68
    • 0242660141 scopus 로고    scopus 로고
    • Dorothy Hodgkin and her Contributions to Biochemistry
    • Howard, J. A. K. Dorothy Hodgkin and her Contributions to Biochemistry Nat. Rev. Mol. Cell Biol. 2003, 4, 891-896 10.1038/nrm1243
    • (2003) Nat. Rev. Mol. Cell Biol. , vol.4 , pp. 891-896
    • Howard, J.A.K.1
  • 71
    • 33947334835 scopus 로고
    • Alkylcobaloximes and Their Relation to Alkylcobalamins
    • Schrauzer, G. N.; Windgassen, R. J. Alkylcobaloximes and Their Relation to Alkylcobalamins J. Am. Chem. Soc. 1966, 88, 3738-3743 10.1021/ja00968a012
    • (1966) J. Am. Chem. Soc. , vol.88 , pp. 3738-3743
    • Schrauzer, G.N.1    Windgassen, R.J.2
  • 72
    • 0001025629 scopus 로고
    • Cobalamin Model Compounds. Preparation and Reactions of Substituted Alkyl- and Alkenylcobaloximes and Biochemical Implications
    • Schrauzer, G. N.; Windgassen, R. J. Cobalamin Model Compounds. Preparation and Reactions of Substituted Alkyl- and Alkenylcobaloximes and Biochemical Implications J. Am. Chem. Soc. 1967, 89, 1999-2007 10.1021/ja00985a006
    • (1967) J. Am. Chem. Soc. , vol.89 , pp. 1999-2007
    • Schrauzer, G.N.1    Windgassen, R.J.2
  • 74
    • 0005186683 scopus 로고
    • Cobalt-Catalyzed Regiospecific Conversion of Aryl-Substituted Olefins into Alcohols using Molecular Oxygen and Tetrahydroborate. The Reaction of Oxygen with Activated Substrates
    • Okamoto, T.; Oka, S. Cobalt-Catalyzed Regiospecific Conversion of Aryl-Substituted Olefins into Alcohols using Molecular Oxygen and Tetrahydroborate. the Reaction of Oxygen with Activated Substrates Tetrahedron Lett. 1981, 22, 2191-2194 10.1016/S0040-4039(01)90495-2
    • (1981) Tetrahedron Lett. , vol.22 , pp. 2191-2194
    • Okamoto, T.1    Oka, S.2
  • 75
    • 33845471665 scopus 로고
    • Oxygenation of Olefins under Reductive Conditions. Cobalt-Catalyzed Selective Conversion of Aromatic Olefins to Benzylic Alcohols by Molecular Oxygen and Tetrahydroborate
    • Okamoto, T.; Oka, S. Oxygenation of Olefins under Reductive Conditions. Cobalt-Catalyzed Selective Conversion of Aromatic Olefins to Benzylic Alcohols by Molecular Oxygen and Tetrahydroborate J. Org. Chem. 1984, 49, 1589-1594 10.1021/jo00183a020
    • (1984) J. Org. Chem. , vol.49 , pp. 1589-1594
    • Okamoto, T.1    Oka, S.2
  • 78
    • 0037567608 scopus 로고    scopus 로고
    • Catalytic Oxygenation of Olefin with Dioxygen and Tetra-t-Butylphthalocyanine Complexes in the Presence of Sodium Borohydride
    • Sugimori, T.; Horike, S.-i.; Tsumura, S.; Handa, M.; Kasuga, K. Catalytic Oxygenation of Olefin with Dioxygen and Tetra-t-Butylphthalocyanine Complexes in the Presence of Sodium Borohydride Inorg. Chim. Acta 1998, 283, 275-278 10.1016/S0020-1693(98)00090-5
    • (1998) Inorg. Chim. Acta , vol.283 , pp. 275-278
    • Sugimori, T.1    Horike, S.-I.2    Tsumura, S.3    Handa, M.4    Kasuga, K.5
  • 79
    • 84885621298 scopus 로고    scopus 로고
    • Phthalocyanine Metal Complexes in Catalysis
    • Sorokin, A. B. Phthalocyanine Metal Complexes in Catalysis Chem. Rev. 2013, 113, 8152-8191 10.1021/cr4000072
    • (2013) Chem. Rev. , vol.113 , pp. 8152-8191
    • Sorokin, A.B.1
  • 80
    • 40149110727 scopus 로고    scopus 로고
    • Direct Coupling of Catharanthine and Vindoline to Provide Vinblastine: Total Synthesis of (+)- and ent-(-)-Vinblastine
    • Ishikawa, H.; Colby, D. A.; Boger, D. L. Direct Coupling of Catharanthine and Vindoline to Provide Vinblastine: Total Synthesis of (+)- and ent-(-)-Vinblastine J. Am. Chem. Soc. 2008, 130, 420-421 10.1021/ja078192m
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 420-421
    • Ishikawa, H.1    Colby, D.A.2    Boger, D.L.3
  • 81
    • 84858665556 scopus 로고    scopus 로고
    • 4-Mediated Additions to Unactivated Alkenes: Synthesis of Novel 20′-Vinblastine Analogues
    • 4-Mediated Additions to Unactivated Alkenes: Synthesis of Novel 20′-Vinblastine Analogues Org. Lett. 2012, 14, 1428-1431 10.1021/ol300173v
    • (2012) Org. Lett. , vol.14 , pp. 1428-1431
    • Leggans, E.K.1    Barker, T.J.2    Duncan, K.K.3    Boger, D.L.4
  • 86
    • 0023835716 scopus 로고
    • Production of 3′, 4′ Anhydrovinblastine: A Unique Chemical Synthesis
    • Vukovic, J.; Goodbody, A. E.; Kutney, J. P.; Misawa, M. Production of 3′, 4′ Anhydrovinblastine: a Unique Chemical Synthesis Tetrahedron 1988, 44, 325-331 10.1016/S0040-4020(01)85824-5
    • (1988) Tetrahedron , vol.44 , pp. 325-331
    • Vukovic, J.1    Goodbody, A.E.2    Kutney, J.P.3    Misawa, M.4
  • 87
    • 73949140641 scopus 로고    scopus 로고
    • Iron-Catalyzed Redox Radical Cyclizations of 1,6-Dienes and Enynes
    • Taniguchi, T.; Goto, N.; Nishibata, A.; Ishibashi, H. Iron-Catalyzed Redox Radical Cyclizations of 1,6-Dienes and Enynes Org. Lett. 2010, 12, 112-115 10.1021/ol902562j
    • (2010) Org. Lett. , vol.12 , pp. 112-115
    • Taniguchi, T.1    Goto, N.2    Nishibata, A.3    Ishibashi, H.4
  • 88
    • 84897586652 scopus 로고    scopus 로고
    • Direct Synthesis of 1,4-Diols from Alkenes by Iron-Catalyzed Aerobic Hydration and C-H Hydroxylation
    • Hashimoto, T.; Hirose, D.; Taniguchi, T. Direct Synthesis of 1,4-Diols from Alkenes by Iron-Catalyzed Aerobic Hydration and C-H Hydroxylation Angew. Chem., Int. Ed. 2014, 53, 2730-2734 10.1002/anie.201308675
    • (2014) Angew. Chem., Int. Ed. , vol.53 , pp. 2730-2734
    • Hashimoto, T.1    Hirose, D.2    Taniguchi, T.3
  • 90
    • 0034722232 scopus 로고    scopus 로고
    • Effect of Anionic Axial Ligands on the Formation of Oxoiron(IV) Porphyrin Intermediates
    • Nam, W.; Lim, M. H.; Oh, S.- Y. Effect of Anionic Axial Ligands on the Formation of Oxoiron(IV) Porphyrin Intermediates Inorg. Chem. 2000, 39, 5572-5575 10.1021/ic000502d
    • (2000) Inorg. Chem. , vol.39 , pp. 5572-5575
    • Nam, W.1    Lim, M.H.2    Oh, S.-Y.3
  • 91
    • 0037100448 scopus 로고    scopus 로고
    • Anionic Ligand Effect on the Nature of Epoxidizing Intermediates in Iron Porphyrin Complex-Catalyzed Epoxidation Reactions
    • Nam, W.; Jin, S. W.; Lim, M. H.; Ryu, J. Y.; Kim, C. Anionic Ligand Effect on the Nature of Epoxidizing Intermediates in Iron Porphyrin Complex-Catalyzed Epoxidation Reactions Inorg. Chem. 2002, 41, 3647-3652 10.1021/ic011145p
    • (2002) Inorg. Chem. , vol.41 , pp. 3647-3652
    • Nam, W.1    Jin, S.W.2    Lim, M.H.3    Ryu, J.Y.4    Kim, C.5
  • 92
    • 0000401994 scopus 로고
    • Novel Catalytic Oxidations of Terminal Olefins by Cobalt(II)-Schiff Base Complexes
    • Zombeck, A.; Hamilton, D. E.; Drago, R. S. Novel Catalytic Oxidations of Terminal Olefins by Cobalt(II)-Schiff Base Complexes J. Am. Chem. Soc. 1982, 104, 6782-6784 10.1021/ja00388a051
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 6782-6784
    • Zombeck, A.1    Hamilton, D.E.2    Drago, R.S.3
  • 93
    • 0000106668 scopus 로고
    • Steric and Electronic Effects of Ligand Variation on Cobalt Dioxygen Catalysis
    • Corden, B. B.; Drago, R. S.; Perito, R. P. Steric and Electronic Effects of Ligand Variation on Cobalt Dioxygen Catalysis J. Am. Chem. Soc. 1985, 107, 2903-2907 10.1021/ja00296a012
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 2903-2907
    • Corden, B.B.1    Drago, R.S.2    Perito, R.P.3
  • 95
    • 0042771133 scopus 로고
    • Coordination of Molecular Oxygen by Cobalt(II) β-Diketonates
    • Talsi, E. P.; Zimin, Y. S.; Nekipelov, V. M. Coordination of Molecular Oxygen by Cobalt(II) β-Diketonates React. Kinet. Catal. Lett. 1985, 27, 361-364 10.1007/BF02070475
    • (1985) React. Kinet. Catal. Lett. , vol.27 , pp. 361-364
    • Talsi, E.P.1    Zimin, Y.S.2    Nekipelov, V.M.3
  • 96
    • 0000699743 scopus 로고
    • Physical and Chemical Properties of Mononuclear Cobalt Dioxygen Complexes with Tetraimidazolyl-Substituted Pyridine Chelates
    • Tamagaki, S.; Kanamaru, Y.; Ueno, M.; Tagaki, W. Physical and Chemical Properties of Mononuclear Cobalt Dioxygen Complexes with Tetraimidazolyl-Substituted Pyridine Chelates Bull. Chem. Soc. Jpn. 1991, 64, 165-174 10.1246/bcsj.64.165
    • (1991) Bull. Chem. Soc. Jpn. , vol.64 , pp. 165-174
    • Tamagaki, S.1    Kanamaru, Y.2    Ueno, M.3    Tagaki, W.4
  • 97
    • 0000030461 scopus 로고
    • Oxidation-Reduction Hydration of Olefins with Molecular Oxygen and 2-Propanol Catalyzed by Bis(acetylacetonato)cobalt(II)
    • Mukaiyama, T.; Isayama, S.; Inoki, S.; Kato, K.; Yamada, T.; Takai, T. Oxidation-Reduction Hydration of Olefins with Molecular Oxygen and 2-Propanol Catalyzed by Bis(acetylacetonato)cobalt(II) Chem. Lett. 1989, 18, 449-452 10.1246/cl.1989.449
    • (1989) Chem. Lett. , vol.18 , pp. 449-452
    • Mukaiyama, T.1    Isayama, S.2    Inoki, S.3    Kato, K.4    Yamada, T.5    Takai, T.6
  • 98
    • 0002405052 scopus 로고
    • Bis(trifluoroacetylacetonato)cobalt(II) Catalyzed Oxidation-Reduction Hydration of Olefins Selective Formation of Alcohols from Olefins
    • Inoki, S.; Kato, K.; Takai, T.; Isayama, S.; Yamada, T.; Mukaiyama, T. Bis(trifluoroacetylacetonato)cobalt(II) Catalyzed Oxidation-Reduction Hydration of Olefins Selective Formation of Alcohols from Olefins Chem. Lett. 1989, 18, 515-518 10.1246/cl.1989.515
    • (1989) Chem. Lett. , vol.18 , pp. 515-518
    • Inoki, S.1    Kato, K.2    Takai, T.3    Isayama, S.4    Yamada, T.5    Mukaiyama, T.6
  • 99
    • 0025313397 scopus 로고
    • Catalytic Oxidation-Reduction Hydration of Olefin with Molecular Oxygen in the Presence of Bis(1,3-diketonato)cobalt(II) Complexes
    • Kato, K.; Yamada, T.; Takai, T.; Inoki, S.; Isayama, S. Catalytic Oxidation-Reduction Hydration of Olefin with Molecular Oxygen in the Presence of Bis(1,3-diketonato)cobalt(II) Complexes Bull. Chem. Soc. Jpn. 1990, 63, 179-186 10.1246/bcsj.63.179
    • (1990) Bull. Chem. Soc. Jpn. , vol.63 , pp. 179-186
    • Kato, K.1    Yamada, T.2    Takai, T.3    Inoki, S.4    Isayama, S.5
  • 100
    • 0000662960 scopus 로고
    • Hydration of Olefins with Molecular Oxygen and Triethylsilane Catalyzed by Bis(trifluoroacetylacetonato)cobalt(II)
    • Isayama, S.; Mukaiyama, T. Hydration of Olefins with Molecular Oxygen and Triethylsilane Catalyzed by Bis(trifluoroacetylacetonato)cobalt(II) Chem. Lett. 1989, 18, 569-572 10.1246/cl.1989.569
    • (1989) Chem. Lett. , vol.18 , pp. 569-572
    • Isayama, S.1    Mukaiyama, T.2
  • 101
    • 0011345676 scopus 로고
    • Reductions with Organosilicon Hydrides. III. Reduction of Acyl Fluorides to Esters
    • Citron, J. D. Reductions with Organosilicon Hydrides. III. Reduction of Acyl Fluorides to Esters J. Org. Chem. 1971, 36, 2547-2548 10.1021/jo00816a038
    • (1971) J. Org. Chem. , vol.36 , pp. 2547-2548
    • Citron, J.D.1
  • 102
    • 0003105070 scopus 로고
    • A Novel Method for the Preparation of Symmetrical and Unsymmetrical Ethers. Trityl Perchlorate Promoted Reduction of Carbonyl Compounds with Triethylsilane
    • Kato, J.-i.; Iwasawa, N.; Mukaiyama, T. A Novel Method for the Preparation of Symmetrical and Unsymmetrical Ethers. Trityl Perchlorate Promoted Reduction of Carbonyl Compounds with Triethylsilane Chem. Lett. 1985, 14, 743-746 10.1246/cl.1985.743
    • (1985) Chem. Lett. , vol.14 , pp. 743-746
    • Kato, J.-I.1    Iwasawa, N.2    Mukaiyama, T.3
  • 103
    • 0002709496 scopus 로고
    • Novel Method for the Preparation of Triethylsilyl Peroxides from Olefins by the Reaction with Molecular Oxygen and Triethylsilane Catalyzed by Bis(1,3-diketonato)cobalt(II)
    • Isayama, S.; Mukaiyama, T. Novel Method for the Preparation of Triethylsilyl Peroxides from Olefins by the Reaction with Molecular Oxygen and Triethylsilane Catalyzed by Bis(1,3-diketonato)cobalt(II) Chem. Lett. 1989, 18, 573-576 10.1246/cl.1989.573
    • (1989) Chem. Lett. , vol.18 , pp. 573-576
    • Isayama, S.1    Mukaiyama, T.2
  • 104
    • 0001695182 scopus 로고
    • An Efficient Method for the Direct Peroxygenation of Various Olefinic Compounds with Molecular Oxygen and Triethylsilane Catalyzed by a Cobalt(II) Complex
    • Isayama, S. An Efficient Method for the Direct Peroxygenation of Various Olefinic Compounds with Molecular Oxygen and Triethylsilane Catalyzed by a Cobalt(II) Complex Bull. Chem. Soc. Jpn. 1990, 63, 1305-1310 10.1246/bcsj.63.1305
    • (1990) Bull. Chem. Soc. Jpn. , vol.63 , pp. 1305-1310
    • Isayama, S.1
  • 105
    • 0000038893 scopus 로고
    • A New Method for Preparation of Alcohols from Olefins with Molecular Oxygen and Phenylsilane by the use of Bis(acetylacetonato)cobalt(II)
    • Isayama, S.; Mukaiyama, T. A New Method for Preparation of Alcohols from Olefins with Molecular Oxygen and Phenylsilane by the use of Bis(acetylacetonato)cobalt(II) Chem. Lett. 1989, 18, 1071-1074 10.1246/cl.1989.1071
    • (1989) Chem. Lett. , vol.18 , pp. 1071-1074
    • Isayama, S.1    Mukaiyama, T.2
  • 106
    • 0003002042 scopus 로고
    • A New and Facile Method for the Direct Preparation of α-Hydroxycarboxylic Acid Esters from α,β-Unsaturated Carboxylic Acid Esters with Molecular Oxygen and Phenylsilane Catalyzed by Bis(dipivaloylmethanato)manganese(II) Complex
    • Inoki, S.; Kato, K.; Isayama, S.; Mukaiyama, T. A New and Facile Method for the Direct Preparation of α-Hydroxycarboxylic Acid Esters from α,β-Unsaturated Carboxylic Acid Esters with Molecular Oxygen and Phenylsilane Catalyzed by Bis(dipivaloylmethanato)manganese(II) Complex Chem. Lett. 1990, 19, 1869-1872 10.1246/cl.1990.1869
    • (1990) Chem. Lett. , vol.19 , pp. 1869-1872
    • Inoki, S.1    Kato, K.2    Isayama, S.3    Mukaiyama, T.4
  • 107
    • 0034627347 scopus 로고    scopus 로고
    • III Catalyst, Phenylsilane and Dioxygen: Acceleration of Conjugate Hydride Reduction by Dioxygen
    • III Catalyst, Phenylsilane and Dioxygen: Acceleration of Conjugate Hydride Reduction by Dioxygen Tetrahedron Lett. 2000, 41, 9725-9730 10.1016/S0040-4039(00)01727-5
    • (2000) Tetrahedron Lett. , vol.41 , pp. 9725-9730
    • Magnus, P.1    Payne, A.H.2    Waring, M.J.3    Scott, D.A.4    Lynch, V.5
  • 109
    • 11844282141 scopus 로고    scopus 로고
    • Stereoselective Preparation of a-Hydroxycarboxamide by Manganese Complex Catalyzed Hydration of α,β-Unsaturated Carboxamide with Molecular Oxygen and Phenylsilane
    • Sato, M.; Gunji, Y.; Ikeno, T.; Yamada, T. Stereoselective Preparation of a-Hydroxycarboxamide by Manganese Complex Catalyzed Hydration of α,β-Unsaturated Carboxamide with Molecular Oxygen and Phenylsilane Chem. Lett. 2004, 33, 1304-1305 10.1246/cl.2004.1304
    • (2004) Chem. Lett. , vol.33 , pp. 1304-1305
    • Sato, M.1    Gunji, Y.2    Ikeno, T.3    Yamada, T.4
  • 110
    • 0033588453 scopus 로고    scopus 로고
    • (Salen)Mn-Catalyzed Oxygenation of Vinyl Arenes to the Corresponding Alcohols in the Presence of Sodium Borohydride
    • Lee, N. H.; Baik, J. S.; Han, S.-b. (Salen)Mn-Catalyzed Oxygenation of Vinyl Arenes to the Corresponding Alcohols in the Presence of Sodium Borohydride Bull. Korean Chem. Soc. 1999, 20, 867-868
    • (1999) Bull. Korean Chem. Soc. , vol.20 , pp. 867-868
    • Lee, N.H.1    Baik, J.S.2    Han, S.-B.3
  • 114
    • 33645219156 scopus 로고    scopus 로고
    • (Schiff-Base)Mn(III)-Catalyzed Hydroxylation of α,β-Unsaturated Esters Using Molecular Oxygen in the Presence of Metal Hydrides
    • Baik, J. S.; Han, S.-b.; Lee, N. H. (Schiff-Base)Mn(III)-Catalyzed Hydroxylation of α,β-Unsaturated Esters Using Molecular Oxygen in the Presence of Metal Hydrides Bull. Korean Chem. Soc. 2006, 27, 333-334 10.5012/bkcs.2006.27.2.333
    • (2006) Bull. Korean Chem. Soc. , vol.27 , pp. 333-334
    • Baik, J.S.1    Han, S.-B.2    Lee, N.H.3
  • 115
    • 33748339796 scopus 로고    scopus 로고
    • Hydrazines and Azides via the Metal-Catalyzed Hydrohydrazination and Hydroazidation of Olefins
    • Waser, J.; Gaspar, B.; Nambu, H.; Carreira, E. M. Hydrazines and Azides via the Metal-Catalyzed Hydrohydrazination and Hydroazidation of Olefins J. Am. Chem. Soc. 2006, 128, 11693-11712 10.1021/ja062355+
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 11693-11712
    • Waser, J.1    Gaspar, B.2    Nambu, H.3    Carreira, E.M.4
  • 116
    • 84964733203 scopus 로고    scopus 로고
    • 2: An Exceptional Reductant for Metal-Catalyzed Hydrogen Atom Transfers
    • 2: An Exceptional Reductant for Metal-Catalyzed Hydrogen Atom Transfers J. Am. Chem. Soc. 2016, 138, 4962-4971 10.1021/jacs.6b02032
    • (2016) J. Am. Chem. Soc. , vol.138 , pp. 4962-4971
    • Obradors, C.1    Martinez, R.M.2    Shenvi, R.A.3
  • 117
    • 0141545220 scopus 로고    scopus 로고
    • Co(thd)2: A Superior Catalyst for Aerobic Epoxidation and Hydroperoxysilylation of Unactivated Alkenes: Application to the Synthesis of Spiro-1,2,4-Trioxanes
    • O'Neill, P. M.; Hindley, S.; Pugh, M. D.; Davies, J.; Bray, P. G.; Park, B. K.; Kapu, D. S.; Ward, S. A.; Stocks, P. A. Co(thd)2: a Superior Catalyst for Aerobic Epoxidation and Hydroperoxysilylation of Unactivated Alkenes: Application to the Synthesis of Spiro-1,2,4-Trioxanes Tetrahedron Lett. 2003, 44, 8135-8138 10.1016/j.tetlet.2003.09.033
    • (2003) Tetrahedron Lett. , vol.44 , pp. 8135-8138
    • O'Neill, P.M.1    Hindley, S.2    Pugh, M.D.3    Davies, J.4    Bray, P.G.5    Park, B.K.6    Kapu, D.S.7    Ward, S.A.8    Stocks, P.A.9
  • 118
    • 0041807557 scopus 로고    scopus 로고
    • Co(III)-Alkyl Complex- and Co(III)-Alkylperoxo Complex-Catalyzed Triethylsilylperoxidation of Alkenes with Molecular Oxygen and Triethylsilane
    • Tokuyasu, T.; Kunikawa, S.; Masuyama, A.; Nojima, M. Co(III)-Alkyl Complex- and Co(III)-Alkylperoxo Complex-Catalyzed Triethylsilylperoxidation of Alkenes with Molecular Oxygen and Triethylsilane Org. Lett. 2002, 4, 3595-3598 10.1021/ol0201299
    • (2002) Org. Lett. , vol.4 , pp. 3595-3598
    • Tokuyasu, T.1    Kunikawa, S.2    Masuyama, A.3    Nojima, M.4
  • 119
    • 24944566770 scopus 로고    scopus 로고
    • Co-catalyzed Autoxidation of Alkene in the Presence of Silane. the Effect of the Structure of Silanes on the Efficiency of the Reaction and on the Product Distribution
    • Wu, J.-M.; Kunikawa, S.; Tokuyasu, T.; Masuyama, A.; Nojima, M.; Kim, H.-S.; Wataya, Y. Co-catalyzed Autoxidation of Alkene in the Presence of Silane. the Effect of the Structure of Silanes on the Efficiency of the Reaction and on the Product Distribution Tetrahedron 2005, 61, 9961-9961 10.1016/j.tet.2005.08.025
    • (2005) Tetrahedron , vol.61 , pp. 9961
    • Wu, J.-M.1    Kunikawa, S.2    Tokuyasu, T.3    Masuyama, A.4    Nojima, M.5    Kim, H.-S.6    Wataya, Y.7
  • 122
    • 0035833052 scopus 로고    scopus 로고
    • Yingzhaosu A Analogues: Synthesis by the Ozonolysis of Unsaturated Hydroperoxides, Structural Analysis and Determination of Anti-Malarial Activity
    • Tokuyasu, T.; Masuyama, A.; Nojima, M.; McCullough, K. J.; Kim, H.-S.; Wataya, Y. Yingzhaosu A Analogues: Synthesis by the Ozonolysis of Unsaturated Hydroperoxides, Structural Analysis and Determination of Anti-Malarial Activity Tetrahedron 2001, 57, 5979-5989 10.1016/S0040-4020(01)00557-9
    • (2001) Tetrahedron , vol.57 , pp. 5979-5989
    • Tokuyasu, T.1    Masuyama, A.2    Nojima, M.3    McCullough, K.J.4    Kim, H.-S.5    Wataya, Y.6
  • 123
    • 0037075833 scopus 로고    scopus 로고
    • Synthesis and Notable Antimalarial Activity of Acyclic Peroxides, 1-(Alkyldioxy)-1-(methyldioxy)cyclododecanes
    • Hamada, Y.; Tokuhara, H.; Masuyama, A.; Nojima, M.; Kim, H.-S.; Ono, K.; Ogura, N.; Wataya, Y. Synthesis and Notable Antimalarial Activity of Acyclic Peroxides, 1-(Alkyldioxy)-1-(methyldioxy)cyclododecanes J. Med. Chem. 2002, 45, 1374-1378 10.1021/jm010473w
    • (2002) J. Med. Chem. , vol.45 , pp. 1374-1378
    • Hamada, Y.1    Tokuhara, H.2    Masuyama, A.3    Nojima, M.4    Kim, H.-S.5    Ono, K.6    Ogura, N.7    Wataya, Y.8
  • 125
    • 0037454656 scopus 로고    scopus 로고
    • Synthesis of Novel Macrocyclic Peroxides by Bis(sym-collidine)iodine (I) Hexafluorophosphate-Mediated Cyclization of Unsaturated Hydroperoxides and Unsaturated Alcohols
    • Ito, T.; Tokuyasu, T.; Masuyama, A.; Nojima, M.; McCullough, K. J. Synthesis of Novel Macrocyclic Peroxides by Bis(sym-collidine)iodine (I) Hexafluorophosphate-Mediated Cyclization of Unsaturated Hydroperoxides and Unsaturated Alcohols Tetrahedron 2003, 59, 525-536 10.1016/S0040-4020(02)01556-9
    • (2003) Tetrahedron , vol.59 , pp. 525-536
    • Ito, T.1    Tokuyasu, T.2    Masuyama, A.3    Nojima, M.4    McCullough, K.J.5
  • 126
    • 84981705272 scopus 로고    scopus 로고
    • Development of New Antimalarial Reagents based on Cyclic Peroxides
    • Masuyama, A.; Nojima, M. Development of New Antimalarial Reagents based on Cyclic Peroxides Kagaku to Kogyo (Osaka, Jpn.) 2005, 79, 250-258
    • (2005) Kagaku to Kogyo (Osaka, Jpn.) , vol.79 , pp. 250-258
    • Masuyama, A.1    Nojima, M.2
  • 127
    • 68949183478 scopus 로고    scopus 로고
    • Synthetic Studies Toward 1,2-Dioxanes as Precursors of Potential Endoperoxide-Containing Antimalarials
    • Gemma, S.; Martí, F.; Gabellieri, E.; Campiani, G.; Novellino, E.; Butini, S. Synthetic Studies Toward 1,2-Dioxanes as Precursors of Potential Endoperoxide-Containing Antimalarials Tetrahedron Lett. 2009, 50, 5719-5722 10.1016/j.tetlet.2009.07.137
    • (2009) Tetrahedron Lett. , vol.50 , pp. 5719-5722
    • Gemma, S.1    Martí, F.2    Gabellieri, E.3    Campiani, G.4    Novellino, E.5    Butini, S.6
  • 129
    • 26444510168 scopus 로고    scopus 로고
    • Intramolecular Reactions of Hydroperoxides and Oxetanes: Stereoselective Synthesis of 1,2-Dioxolanes and 1,2-Dioxanes
    • Dai, P.; Dussault, P. H. Intramolecular Reactions of Hydroperoxides and Oxetanes: Stereoselective Synthesis of 1,2-Dioxolanes and 1,2-Dioxanes Org. Lett. 2005, 7, 4333-4335 10.1021/ol051407h
    • (2005) Org. Lett. , vol.7 , pp. 4333-4335
    • Dai, P.1    Dussault, P.H.2
  • 130
    • 84859608304 scopus 로고    scopus 로고
    • Exploratory Studies toward the Synthesis of Peroxylactone Unit of Plakortolides
    • Barnych, B.; Vatèle, J.-M. Exploratory Studies toward the Synthesis of Peroxylactone Unit of Plakortolides Tetrahedron 2012, 68, 3717-3724 10.1016/j.tet.2012.03.024
    • (2012) Tetrahedron , vol.68 , pp. 3717-3724
    • Barnych, B.1    Vatèle, J.-M.2
  • 131
    • 48849096556 scopus 로고    scopus 로고
    • Synthesis of Spiro-bisperoxyketals
    • Ghorai, P.; Dussault, P. H.; Hu, C. Synthesis of Spiro-bisperoxyketals Org. Lett. 2008, 10, 2401-2404 10.1021/ol800657m
    • (2008) Org. Lett. , vol.10 , pp. 2401-2404
    • Ghorai, P.1    Dussault, P.H.2    Hu, C.3
  • 132
    • 0032503997 scopus 로고    scopus 로고
    • Stereospecific Synthesis of 1,2-Dioxolanes by Alkoxy Radical β-Fragmentation of Steroidal Cyclic Peroxyhemiacetals
    • Boto, A.; Hernández, R.; Velázquez, S. M.; Suárez, E.; Prangé, T. Stereospecific Synthesis of 1,2-Dioxolanes by Alkoxy Radical β-Fragmentation of Steroidal Cyclic Peroxyhemiacetals J. Org. Chem. 1998, 63, 4697-4705 10.1021/jo980319q
    • (1998) J. Org. Chem. , vol.63 , pp. 4697-4705
    • Boto, A.1    Hernández, R.2    Velázquez, S.M.3    Suárez, E.4    Prangé, T.5
  • 134
    • 2342447393 scopus 로고    scopus 로고
    • Recent Advances in Artemisinin and Its Derivatives as Antimalarial and Antitumor Agents
    • Jung, M.; Lee, K.; Kim, H.; Park, M. Recent Advances in Artemisinin and Its Derivatives as Antimalarial and Antitumor Agents Curr. Med. Chem. 2004, 11, 1265-1284 10.2174/0929867043365233
    • (2004) Curr. Med. Chem. , vol.11 , pp. 1265-1284
    • Jung, M.1    Lee, K.2    Kim, H.3    Park, M.4
  • 135
    • 79951774418 scopus 로고    scopus 로고
    • Schistosoma japonicum-Infected Hamsters (Mesocricetus auratus) used as a Model in Experimental Chemotherapy with Praziquantel, Artemether, and OZ Compounds
    • Xiao, S.-h.; Mei, J.-y.; Jiao, P.-y. Schistosoma japonicum-Infected Hamsters (Mesocricetus auratus) used as a Model in Experimental Chemotherapy with Praziquantel, Artemether, and OZ Compounds Parasitol. Res. 2011, 108, 431-437 10.1007/s00436-010-2084-7
    • (2011) Parasitol. Res. , vol.108 , pp. 431-437
    • Xiao, S.-H.1    Mei, J.-Y.2    Jiao, P.-Y.3
  • 139
    • 0035797060 scopus 로고    scopus 로고
    • Regioselective Mukaiyama hydroperoxysilylation of 2-alkyl- or 2-aryl-prop-2-en-1-ols: Application to the synthesis of 1,2,4-trioxanes
    • O'Neill, P. M.; Pugh, M.; Davies, J.; Ward, S. A.; Park, B. K. Regioselective Mukaiyama hydroperoxysilylation of 2-alkyl- or 2-aryl-prop-2-en-1-ols: application to the synthesis of 1,2,4-trioxanes Tetrahedron Lett. 2001, 42, 4569-4571 10.1016/S0040-4039(01)00791-2
    • (2001) Tetrahedron Lett. , vol.42 , pp. 4569-4571
    • O'Neill, P.M.1    Pugh, M.2    Davies, J.3    Ward, S.A.4    Park, B.K.5
  • 140
    • 0032580458 scopus 로고    scopus 로고
    • A Convenient Synthesis of Substituted 1,2,4-Trioxepanes via Co(II) Catalyzed Oxygenation of Cinnamyl Alcohol
    • Oh, C. H.; Kang, J. H. A Convenient Synthesis of Substituted 1,2,4-Trioxepanes via Co(II) Catalyzed Oxygenation of Cinnamyl Alcohol Tetrahedron Lett. 1998, 39, 2771-2774 10.1016/S0040-4039(98)00335-9
    • (1998) Tetrahedron Lett. , vol.39 , pp. 2771-2774
    • Oh, C.H.1    Kang, J.H.2
  • 142
    • 84891923837 scopus 로고    scopus 로고
    • Synthesis of Five- and Six-Membered Cyclic Organic Peroxides: Key Transformations into Peroxide Ring-Retaining Products
    • Terent'ev, A. O.; Borisov, D. A.; Vil', V. A.; Dembitsky, V. M. Synthesis of Five- and Six-Membered Cyclic Organic Peroxides: Key Transformations into Peroxide Ring-Retaining Products Beilstein J. Org. Chem. 2014, 10, 34-114 10.3762/bjoc.10.6
    • (2014) Beilstein J. Org. Chem. , vol.10 , pp. 34-114
    • Terent'Ev, A.O.1    Borisov, D.A.2    Vil, V.A.3    Dembitsky, V.M.4
  • 143
    • 0034964979 scopus 로고    scopus 로고
    • Recent Advances in the Chemistry of Cyclic Peroxides
    • McCullough, K. J.; Nojima, M. Recent Advances in the Chemistry of Cyclic Peroxides Curr. Org. Chem. 2001, 5, 601-636 10.2174/1385272013375346
    • (2001) Curr. Org. Chem. , vol.5 , pp. 601-636
    • McCullough, K.J.1    Nojima, M.2
  • 144
    • 84906232252 scopus 로고    scopus 로고
    • Synthesis of Silyl Monoperoxyketals by Regioselective Cobalt-Catalyzed Peroxidation of Silyl Enol Ethers: Application to the Synthesis of 1,2-Dioxolanes
    • Hurlocker, B.; Miner, M. R.; Woerpel, K. A. Synthesis of Silyl Monoperoxyketals by Regioselective Cobalt-Catalyzed Peroxidation of Silyl Enol Ethers: Application to the Synthesis of 1,2-Dioxolanes Org. Lett. 2014, 16, 4280-4283 10.1021/ol5020015
    • (2014) Org. Lett. , vol.16 , pp. 4280-4283
    • Hurlocker, B.1    Miner, M.R.2    Woerpel, K.A.3
  • 145
    • 84940191291 scopus 로고    scopus 로고
    • N1-type Reaction to Form the 1,2-Dioxepane Ring: Synthesis of 10,12-Peroxycalamenene
    • N1-type Reaction to Form the 1,2-Dioxepane Ring: Synthesis of 10,12-Peroxycalamenene J. Org. Chem. 2015, 80, 8262-8267 10.1021/acs.joc.5b01326
    • (2015) J. Org. Chem. , vol.80 , pp. 8262-8267
    • Hilf, J.A.1    Witthoft, L.W.2    Woerpel, K.A.3
  • 146
    • 0000179292 scopus 로고
    • Cobalt(II) Porphyrin-Catalyzed Oxidation of Olefins to Ketones with Molecular Oxygen and Triethylsilane in 2-Propanol
    • Matsushita, Y.-i.; Matsui, T.; Sugamoto, K. Cobalt(II) Porphyrin-Catalyzed Oxidation of Olefins to Ketones with Molecular Oxygen and Triethylsilane in 2-Propanol Chem. Lett. 1992, 21, 1381-1384 10.1246/cl.1992.1381
    • (1992) Chem. Lett. , vol.21 , pp. 1381-1384
    • Matsushita, Y.-I.1    Matsui, T.2    Sugamoto, K.3
  • 147
    • 0002936764 scopus 로고
    • Novel Method for Preparation of 4-Oxo-2-alkenoic Acid Derivatives from 2,4-Alkadienoic Acid Derivatives by Cobalt(II) Porphyrin-catalyzed Oxygenation
    • Matsushita, Y.-i.; Sugamoto, K.; Matsui, T. Novel Method for Preparation of 4-Oxo-2-alkenoic Acid Derivatives from 2,4-Alkadienoic Acid Derivatives by Cobalt(II) Porphyrin-catalyzed Oxygenation Chem. Lett. 1992, 21, 2165-2168 10.1246/cl.1992.2165
    • (1992) Chem. Lett. , vol.21 , pp. 2165-2168
    • Matsushita, Y.-I.1    Sugamoto, K.2    Matsui, T.3
  • 148
    • 2142654389 scopus 로고
    • One-Pot Preparation of Alcohols from Aromatic Olefins and Acrylic Acid Derivatives by Cobalt(II) Porphyrin-Catalyzed Reductive Oxygenation Followed by Reduction with Trimethyl Phosphite
    • Matsusita, Y.-i.; Sugamoto, K.; Matsui, T. One-Pot Preparation of Alcohols from Aromatic Olefins and Acrylic Acid Derivatives by Cobalt(II) Porphyrin-Catalyzed Reductive Oxygenation Followed by Reduction with Trimethyl Phosphite Chem. Lett. 1993, 22, 925-928 10.1246/cl.1993.925
    • (1993) Chem. Lett. , vol.22 , pp. 925-928
    • Matsushita, Y.-I.1    Sugamoto, K.2    Matsui, T.3
  • 149
    • 37049077114 scopus 로고
    • Synthesis of γ-Hydroperoxy-a,b-Unsaturated Carbonyl Compounds from α,β,γ-Unsaturated Carbonyl Compounds by Cobalt(II) Porphyrin-catalysed Hydroperoxygenation
    • Matsushita, Y.-i.; Sugamoto, K.; Nakama, T.; Matsui, T. Synthesis of γ-Hydroperoxy-a,b-Unsaturated Carbonyl Compounds from α,β,γ-Unsaturated Carbonyl Compounds by Cobalt(II) Porphyrin-catalysed Hydroperoxygenation J. Chem. Soc., Chem. Commun. 1995, 567-568 10.1039/C39950000567
    • (1995) J. Chem. Soc., Chem. Commun. , pp. 567-568
    • Matsushita, Y.-I.1    Sugamoto, K.2    Nakama, T.3    Matsui, T.4
  • 150
    • 0028925931 scopus 로고
    • γ-Selective Hydroxylation of α,β,γ-Unsaturated Carbonyl Compounds and its Application to Syntheses of (±)-6-Hydroxyshogaol and Related Furanoids
    • Matsushita, Y.-i.; Sugamoto, K.; Nakama, T.; Sakamoto, T.; Matsui, T.; Nakayama, M. γ-Selective Hydroxylation of α,β,γ-Unsaturated Carbonyl Compounds and its Application to Syntheses of (±)-6-Hydroxyshogaol and Related Furanoids Tetrahedron Lett. 1995, 36, 1879-1882 10.1016/0040-4039(95)00173-A
    • (1995) Tetrahedron Lett. , vol.36 , pp. 1879-1882
    • Matsushita, Y.-I.1    Sugamoto, K.2    Nakama, T.3    Sakamoto, T.4    Matsui, T.5    Nakayama, M.6
  • 151
    • 0041577831 scopus 로고    scopus 로고
    • Direct Hydroperoxygenation of Conjugated Olefins Catalyzed by Cobalt(II) Porphyrin
    • Sugamoto, K.; Matsushita, Y.-i.; Matsui, T. Direct Hydroperoxygenation of Conjugated Olefins Catalyzed by Cobalt(II) Porphyrin J. Chem. Soc., Perkin Trans. 1 1998, 3989-3998 10.1039/a805888a
    • (1998) J. Chem. Soc., Perkin Trans. 1 , pp. 3989-3998
    • Sugamoto, K.1    Matsushita, Y.-I.2    Matsui, T.3
  • 152
    • 0012284077 scopus 로고
    • A Convenient Method for the Direct Preparation of Ketones from Vinylsilanes with Molecular Oxygen Catalyzed by a Cobalt(II) Complex
    • Kato, K.; Mukaiyama, T. A Convenient Method for the Direct Preparation of Ketones from Vinylsilanes with Molecular Oxygen Catalyzed by a Cobalt(II) Complex Chem. Lett. 1989, 18, 2233-2236 10.1246/cl.1989.2233
    • (1989) Chem. Lett. , vol.18 , pp. 2233-2236
    • Kato, K.1    Mukaiyama, T.2
  • 153
    • 0033575445 scopus 로고    scopus 로고
    • 1,5-Induction in Reactions of 4-Alkoxy-2-trimethylsilylalk-2-enyl(tributyl)stannanes with Aldehydes
    • Taylor, N. H.; Thomas, E. J. 1,5-Induction in Reactions of 4-Alkoxy-2-trimethylsilylalk-2-enyl(tributyl)stannanes with Aldehydes Tetrahedron 1999, 55, 8757-8768 10.1016/S0040-4020(99)00442-1
    • (1999) Tetrahedron , vol.55 , pp. 8757-8768
    • Taylor, N.H.1    Thomas, E.J.2
  • 155
    • 84954357113 scopus 로고    scopus 로고
    • Symmetry-Driven Strategy for the Assembly of the Core Tetracycle of (+)-Ryanodine: Synthetic Utility of a Cobalt-Catalyzed Olefin Oxidation and α-Alkoxy Bridgehead Radical Reaction
    • Nagatomo, M.; Hagiwara, K.; Masuda, K.; Koshimizu, M.; Kawamata, T.; Matsui, Y.; Urabe, D.; Inoue, M. Symmetry-Driven Strategy for the Assembly of the Core Tetracycle of (+)-Ryanodine: Synthetic Utility of a Cobalt-Catalyzed Olefin Oxidation and α-Alkoxy Bridgehead Radical Reaction Chem.-Eur. J. 2016, 22, 222-229 10.1002/chem.201503640
    • (2016) Chem. - Eur. J. , vol.22 , pp. 222-229
    • Nagatomo, M.1    Hagiwara, K.2    Masuda, K.3    Koshimizu, M.4    Kawamata, T.5    Matsui, Y.6    Urabe, D.7    Inoue, M.8
  • 156
    • 84880358874 scopus 로고    scopus 로고
    • Hydroalkoxylation of Unactivated Olefins with Carbon Radicals and Carbocation Species as Key Intermediates
    • Shigehisa, H.; Aoki, T.; Yamaguchi, S.; Shimizu, N.; Hiroya, K. Hydroalkoxylation of Unactivated Olefins with Carbon Radicals and Carbocation Species as Key Intermediates J. Am. Chem. Soc. 2013, 135, 10306-10309 10.1021/ja405219f
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 10306-10309
    • Shigehisa, H.1    Aoki, T.2    Yamaguchi, S.3    Shimizu, N.4    Hiroya, K.5
  • 157
    • 84946495555 scopus 로고    scopus 로고
    • Functional Group Tolerant Markovnikov-Selective Hydrofunctionalization of Unactivated Olefins Using a Cobalt Complex as Catalyst
    • Shigehisa, H. Functional Group Tolerant Markovnikov-Selective Hydrofunctionalization of Unactivated Olefins Using a Cobalt Complex as Catalyst Synlett 2015, 26, 2479-2484 10.1055/s-0035-1560171
    • (2015) Synlett , vol.26 , pp. 2479-2484
    • Shigehisa, H.1
  • 158
    • 84964788399 scopus 로고    scopus 로고
    • Markovnikov-Selective Addition of Fluorous Solvents to Unactivated Olefins Using a Co Catalyst
    • Shigehisa, H.; Kikuchi, H.; Hiroya, K. Markovnikov-Selective Addition of Fluorous Solvents to Unactivated Olefins Using a Co Catalyst Chem. Pharm. Bull. 2016, 64, 371-374 10.1248/cpb.c15-01024
    • (2016) Chem. Pharm. Bull. , vol.64 , pp. 371-374
    • Shigehisa, H.1    Kikuchi, H.2    Hiroya, K.3
  • 159
    • 0035812801 scopus 로고    scopus 로고
    • Donor and Acceptor Properties of the Chromium Tricarbonyl Substitutent in Benzylic and Homobenzylic Anions, Cations and Radicals
    • Merlic, C. A.; Hietbrink, B. N.; Houk, K. N. Donor and Acceptor Properties of the Chromium Tricarbonyl Substitutent in Benzylic and Homobenzylic Anions, Cations and Radicals J. Org. Chem. 2001, 66, 6738-6744 10.1021/jo010620y
    • (2001) J. Org. Chem. , vol.66 , pp. 6738-6744
    • Merlic, C.A.1    Hietbrink, B.N.2    Houk, K.N.3
  • 160
    • 0043080677 scopus 로고
    • Total Synthesis of (-)-Pyrenophorin via Cobalt(II) Porphyrin-Catalyzed Oxygenation of Ethyl (2E,4E,7R)-7-Acetoxy-2,4-octadienoate
    • Matsushita, Y.-i.; Furusawa, H.; Matsui, T.; Nakayama, M. Total Synthesis of (-)-Pyrenophorin via Cobalt(II) Porphyrin-Catalyzed Oxygenation of Ethyl (2E,4E,7R)-7-Acetoxy-2,4-octadienoate Chem. Lett. 1994, 23, 1083-1084 10.1246/cl.1994.1083
    • (1994) Chem. Lett. , vol.23 , pp. 1083-1084
    • Matsushita, Y.-I.1    Furusawa, H.2    Matsui, T.3    Nakayama, M.4
  • 161
    • 0030741107 scopus 로고    scopus 로고
    • Enantioselective Syntheses of 10-Oxo-11(E)-octadecen-13-olide and Related Fatty Acid
    • Matsushita, Y.-i.; Sugamoto, K.; Nakama, T.; Matsui, T.; Hayashi, Y.; Uenakai, K. Enantioselective Syntheses of 10-Oxo-11(E)-octadecen-13-olide and Related Fatty Acid Tetrahedron Lett. 1997, 38, 6055-6058 10.1016/S0040-4039(97)01359-2
    • (1997) Tetrahedron Lett. , vol.38 , pp. 6055-6058
    • Matsushita, Y.-I.1    Sugamoto, K.2    Nakama, T.3    Matsui, T.4    Hayashi, Y.5    Uenakai, K.6
  • 162
    • 0011831846 scopus 로고
    • First Total Synthesis of Optically Pure Metabolites of Gomisin A
    • Tanaka, M.; Mitsuhashi, H.; Maruno, M.; Wakamatsu, T. First Total Synthesis of Optically Pure Metabolites of Gomisin A Synlett 1994, 1994, 604-606 10.1055/s-1994-22942
    • (1994) Synlett , vol.1994 , pp. 604-606
    • Tanaka, M.1    Mitsuhashi, H.2    Maruno, M.3    Wakamatsu, T.4
  • 163
    • 0028864840 scopus 로고
    • Total Syntheses of the Metabolites of Schizandrin
    • Tanaka, M.; Ikeya, Y.; Mitsuhashi, H.; Maruno, M.; Wakamatsu, T. Total Syntheses of the Metabolites of Schizandrin Tetrahedron 1995, 51, 11703-11724 10.1016/0040-4020(95)00702-A
    • (1995) Tetrahedron , vol.51 , pp. 11703-11724
    • Tanaka, M.1    Ikeya, Y.2    Mitsuhashi, H.3    Maruno, M.4    Wakamatsu, T.5
  • 164
    • 0029144553 scopus 로고
    • Synthesis of Optically Pure Gomisi Lignans: The Total Synthesis of (+)-Schizandrin, (+)-Gomisin A, and (+)-Isoschizandrin in Naturally Occurring Forms
    • Tanaka, M.; Mukaiyama, C.; Mitsuhashi, H.; Maruno, M.; Wakamatsu, T. Synthesis of Optically Pure Gomisi Lignans: The Total Synthesis of (+)-Schizandrin, (+)-Gomisin A, and (+)-Isoschizandrin in Naturally Occurring Forms J. Org. Chem. 1995, 60, 4339-4352 10.1021/jo00119a010
    • (1995) J. Org. Chem. , vol.60 , pp. 4339-4352
    • Tanaka, M.1    Mukaiyama, C.2    Mitsuhashi, H.3    Maruno, M.4    Wakamatsu, T.5
  • 165
    • 1842741055 scopus 로고    scopus 로고
    • Total Synthesis of the Major Metabolites of Gomisin A. Synthesis of Homochiral Met A-II, Met A-III, and Met F
    • Wakamatsu, T.; Tanaka, M.; Mitsuhashi, H.; Maruno, M. Total Synthesis of the Major Metabolites of Gomisin A. Synthesis of Homochiral Met A-II, Met A-III, and Met F Heterocycles 1996, 42, 359-374 10.3987/COM-95-S45
    • (1996) Heterocycles , vol.42 , pp. 359-374
    • Wakamatsu, T.1    Tanaka, M.2    Mitsuhashi, H.3    Maruno, M.4
  • 166
    • 0006043219 scopus 로고
    • Enantioselective Total Synthesis of a Natural Norsesquiterpene of the Calamene Group by a Silane-Terminated Intramolecular Heck Reaction
    • Tietze, L. F.; Raschke, T. Enantioselective Total Synthesis of a Natural Norsesquiterpene of the Calamene Group by a Silane-Terminated Intramolecular Heck Reaction Synlett 1995, 1995, 597-598 10.1055/s-1995-5016
    • (1995) Synlett , vol.1995 , pp. 597-598
    • Tietze, L.F.1    Raschke, T.2
  • 167
    • 0029075624 scopus 로고
    • Enantioselective Total Syntheses and Stereochemical Studies of All Four Stereoisomers of Yingzhaosu C
    • Xu, X.-X.; Dong, H.-Q. Enantioselective Total Syntheses and Stereochemical Studies of All Four Stereoisomers of Yingzhaosu C J. Org. Chem. 1995, 60, 3039-3044 10.1021/jo00115a019
    • (1995) J. Org. Chem. , vol.60 , pp. 3039-3044
    • Xu, X.-X.1    Dong, H.-Q.2
  • 168
    • 0033678188 scopus 로고    scopus 로고
    • First Asymmetric Synthesis of Stigmolone: The Fruiting Body Inducing Pheromone of the Myxobacterium Stigmatella Aurantiaca
    • Enders, D.; Ridder, A. First Asymmetric Synthesis of Stigmolone: The Fruiting Body Inducing Pheromone of the Myxobacterium Stigmatella Aurantiaca Synthesis 2000, 2000, 1848-1851 10.1055/s-2000-8219
    • (2000) Synthesis , vol.2000 , pp. 1848-1851
    • Enders, D.1    Ridder, A.2
  • 169
    • 0000434949 scopus 로고
    • Morrision, J. D. Academic: Orlando, FL
    • Enders, D. In Asymmetric Synthesis; Morrision, J. D., Ed.; Academic: Orlando, FL, 1984; Vol. 3B, p 275.
    • (1984) Asymmetric Synthesis , vol.3 , pp. 275
    • Enders, D.1
  • 170
    • 0034598053 scopus 로고    scopus 로고
    • Synthesis of (±)-Lahadinine B and (±)-11-Methoxykopsilongine
    • Magnus, P.; Westlund, N. Synthesis of (±)-Lahadinine B and (±)-11-Methoxykopsilongine Tetrahedron Lett. 2000, 41, 9369-9372 10.1016/S0040-4039(00)01399-X
    • (2000) Tetrahedron Lett. , vol.41 , pp. 9369-9372
    • Magnus, P.1    Westlund, N.2
  • 171
    • 0035808936 scopus 로고    scopus 로고
    • Synthesis of (±)-Demethoxypauciflorine B and (±)-Pauciflorine B from (±)-11,12-Demethoxylahadinine B and (±)-Lahadinine B, Respectively via a Peroxycarbanolamine Fragmentation Reaction
    • Magnus, P.; Hobson, L. A.; Westlund, N.; Lynch, V. Synthesis of (±)-Demethoxypauciflorine B and (±)-Pauciflorine B from (±)-11,12-Demethoxylahadinine B and (±)-Lahadinine B, Respectively via a Peroxycarbanolamine Fragmentation Reaction Tetrahedron Lett. 2001, 42, 993-997 10.1016/S0040-4039(00)02218-8
    • (2001) Tetrahedron Lett. , vol.42 , pp. 993-997
    • Magnus, P.1    Hobson, L.A.2    Westlund, N.3    Lynch, V.4
  • 172
    • 0037156634 scopus 로고    scopus 로고
    • Synthesis of the Kopsia Alkaloids (±)-Pauciflorine B, (±)-Lahadinine B, (±)-Kopsidasine, (±)-Kopsidasine-N-oxide, (±)-Kopsijasminilam and (±)-11-Methoxykopsilongine
    • Magnus, P.; Gazzard, L.; Hobson, L.; Payne, A. H.; Rainey, T. J.; Westlund, N.; Lynch, V. Synthesis of the Kopsia Alkaloids (±)-Pauciflorine B, (±)-Lahadinine B, (±)-Kopsidasine, (±)-Kopsidasine-N-oxide, (±)-Kopsijasminilam and (±)-11-Methoxykopsilongine Tetrahedron 2002, 58, 3423-3443 10.1016/S0040-4020(02)00243-0
    • (2002) Tetrahedron , vol.58 , pp. 3423-3443
    • Magnus, P.1    Gazzard, L.2    Hobson, L.3    Payne, A.H.4    Rainey, T.J.5    Westlund, N.6    Lynch, V.7
  • 173
    • 0348225236 scopus 로고    scopus 로고
    • Combined Biological and Chemical Catalysis in the Preparation of Oxycodone
    • Walker, A. J.; Bruce, N. C. Combined Biological and Chemical Catalysis in the Preparation of Oxycodone Tetrahedron 2004, 60, 561-568 10.1016/j.tet.2003.11.063
    • (2004) Tetrahedron , vol.60 , pp. 561-568
    • Walker, A.J.1    Bruce, N.C.2
  • 174
    • 18844417940 scopus 로고    scopus 로고
    • Pectenotoxin-2 Synthetic Studies. 2. Construction and Conjoining of ABC and de Eastern Hemisphere Subtargets
    • Bondar, D.; Liu, J.; Müller, T.; Paquette, L. A. Pectenotoxin-2 Synthetic Studies. 2. Construction and Conjoining of ABC and DE Eastern Hemisphere Subtargets Org. Lett. 2005, 7, 1813-1816 10.1021/ol0504291
    • (2005) Org. Lett. , vol.7 , pp. 1813-1816
    • Bondar, D.1    Liu, J.2    Müller, T.3    Paquette, L.A.4
  • 175
    • 33750528963 scopus 로고    scopus 로고
    • Synthetic Studies Towards the Pectenotoxins: A Review
    • Halim, R.; Brimble, M. A. Synthetic Studies Towards the Pectenotoxins: a Review Org. Biomol. Chem. 2006, 4, 4048-4058 10.1039/b611531b
    • (2006) Org. Biomol. Chem. , vol.4 , pp. 4048-4058
    • Halim, R.1    Brimble, M.A.2
  • 177
    • 80052400158 scopus 로고    scopus 로고
    • Synthetic Efforts Toward [3.3.1] Bridged Bicyclic Phloroglucinol Natural Products
    • Njardarson, J. T. Synthetic Efforts Toward [3.3.1] Bridged Bicyclic Phloroglucinol Natural Products Tetrahedron 2011, 67, 7631-7666 10.1016/j.tet.2011.06.079
    • (2011) Tetrahedron , vol.67 , pp. 7631-7666
    • Njardarson, J.T.1
  • 179
    • 70349784889 scopus 로고    scopus 로고
    • Stereodivergent Synthesis of 17-α and 17-β-Aryl Steroids: Application and Biological Evaluation of D-Ring Cortistatin Analogues
    • Shi, J.; Shigehisa, H.; Guerrero, C. A.; Shenvi, R. A.; Li, C.-C.; Baran, P. S. Stereodivergent Synthesis of 17-α and 17-β-Aryl Steroids: Application and Biological Evaluation of D-Ring Cortistatin Analogues Angew. Chem., Int. Ed. 2009, 48, 4328-4331 10.1002/anie.200901116
    • (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 4328-4331
    • Shi, J.1    Shigehisa, H.2    Guerrero, C.A.3    Shenvi, R.A.4    Li, C.-C.5    Baran, P.S.6
  • 181
    • 77953805522 scopus 로고    scopus 로고
    • Chemistry of the Cortistatins- a Novel Class of Anti-Angiogenic Agents
    • Chen, D. Y.-K.; Tseng, C.-C. Chemistry of the Cortistatins- a Novel Class of Anti-Angiogenic Agents Org. Biomol. Chem. 2010, 8, 2900-2911 10.1039/c003935g
    • (2010) Org. Biomol. Chem. , vol.8 , pp. 2900-2911
    • Chen, D.Y.-K.1    Tseng, C.-C.2
  • 182
    • 57349163298 scopus 로고    scopus 로고
    • Enantioselective Synthesis of the Core of Banyaside, Suomilide, and Spumigin HKVV
    • Schindler, C. S.; Stephenson, C. R. J.; Carreira, E. M. Enantioselective Synthesis of the Core of Banyaside, Suomilide, and Spumigin HKVV Angew. Chem., Int. Ed. 2008, 47, 8852-8855 10.1002/anie.200803655
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 8852-8855
    • Schindler, C.S.1    Stephenson, C.R.J.2    Carreira, E.M.3
  • 183
    • 78649607142 scopus 로고    scopus 로고
    • Total Synthesis of Nominal Banyaside B: Structural Revision of the Glycosylation Site
    • Schindler, C. S.; Bertschi, l.; Carreira, E. M. Total Synthesis of Nominal Banyaside B: Structural Revision of the Glycosylation Site Angew. Chem., Int. Ed. 2010, 49, 9229-9232 10.1002/anie.201004047
    • (2010) Angew. Chem., Int. Ed. , vol.49 , pp. 9229-9232
    • Schindler, C.S.1    Bertschi, L.2    Carreira, E.M.3
  • 184
    • 77953636730 scopus 로고    scopus 로고
    • Total Synthesis and Evaluation of a Key Series of C5-Substituted Vinblastine Derivatives
    • Va, P.; Campbell, E. L.; Robertson, W. M.; Boger, D. L. Total Synthesis and Evaluation of a Key Series of C5-Substituted Vinblastine Derivatives J. Am. Chem. Soc. 2010, 132, 8489-8495 10.1021/ja1027748
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 8489-8495
    • Va, P.1    Campbell, E.L.2    Robertson, W.M.3    Boger, D.L.4
  • 185
    • 77957154690 scopus 로고    scopus 로고
    • Asymmetric Total Synthesis of Vindorosine, Vindoline, and Key Vinblastine Analogues
    • Sasaki, Y.; Kato, D.; Boger, D. L. Asymmetric Total Synthesis of Vindorosine, Vindoline, and Key Vinblastine Analogues J. Am. Chem. Soc. 2010, 132, 13533-13544 10.1021/ja106284s
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 13533-13544
    • Sasaki, Y.1    Kato, D.2    Boger, D.L.3
  • 186
    • 83455258222 scopus 로고    scopus 로고
    • 10′-Fluorovinblastine and 10′-Fluorovincristine: Synthesis of a Key Series of Modified Vinca Alkaloids
    • Gotoh, H.; Duncan, K. K.; Robertson, W. M.; Boger, D. L. 10′-Fluorovinblastine and 10′-Fluorovincristine: Synthesis of a Key Series of Modified Vinca Alkaloids ACS Med. Chem. Lett. 2011, 2, 948-952 10.1021/ml200236a
    • (2011) ACS Med. Chem. Lett. , vol.2 , pp. 948-952
    • Gotoh, H.1    Duncan, K.K.2    Robertson, W.M.3    Boger, D.L.4
  • 187
    • 84885457038 scopus 로고    scopus 로고
    • Potent Vinblastine C20′ Ureas Displaying Additionally Improved Activity Against a Vinblastine-Resistant Cancer Cell Line
    • Barker, T. J.; Duncan, K. K.; Otrubova, K.; Boger, D. L. Potent Vinblastine C20′ Ureas Displaying Additionally Improved Activity Against a Vinblastine-Resistant Cancer Cell Line ACS Med. Chem. Lett. 2013, 4, 985-988 10.1021/ml400281w
    • (2013) ACS Med. Chem. Lett. , vol.4 , pp. 985-988
    • Barker, T.J.1    Duncan, K.K.2    Otrubova, K.3    Boger, D.L.4
  • 188
    • 84872772908 scopus 로고    scopus 로고
    • A Remarkable Series of Vinblastine Analogues Displaying Enhanced Activity and an Unprecedented Tubulin Binding Steric Tolerance: C20′ Urea Derivatives
    • Leggans, E. K.; Duncan, K. K.; Barker, T. J.; Schleicher, K. D.; Boger, D. L. A Remarkable Series of Vinblastine Analogues Displaying Enhanced Activity and an Unprecedented Tubulin Binding Steric Tolerance: C20′ Urea Derivatives J. Med. Chem. 2013, 56, 628-639 10.1021/jm3015684
    • (2013) J. Med. Chem. , vol.56 , pp. 628-639
    • Leggans, E.K.1    Duncan, K.K.2    Barker, T.J.3    Schleicher, K.D.4    Boger, D.L.5
  • 189
    • 84872818405 scopus 로고    scopus 로고
    • Total Synthesis and Evaluation of Vinblastine Analogues Containing Systematic Deep-Seated Modifications in the Vindoline Subunit Ring System: Core Redesign
    • Schleicher, K. D.; Sasaki, Y.; Tam, A.; Kato, D.; Duncan, K. K.; Boger, D. L. Total Synthesis and Evaluation of Vinblastine Analogues Containing Systematic Deep-Seated Modifications in the Vindoline Subunit Ring System: Core Redesign J. Med. Chem. 2013, 56, 483-495 10.1021/jm3014376
    • (2013) J. Med. Chem. , vol.56 , pp. 483-495
    • Schleicher, K.D.1    Sasaki, Y.2    Tam, A.3    Kato, D.4    Duncan, K.K.5    Boger, D.L.6
  • 190
  • 192
    • 79961223193 scopus 로고    scopus 로고
    • Total Synthesis of (+)-Omphadiol
    • Liu, G.; Romo, D. Total Synthesis of (+)-Omphadiol Angew. Chem., Int. Ed. 2011, 50, 7537-7540 10.1002/anie.201102289
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 7537-7540
    • Liu, G.1    Romo, D.2
  • 193
    • 79953231987 scopus 로고    scopus 로고
    • Toward the Total Synthesis of Maoecrystal V: An Intramolecular Diels-Alder Route to the Maoecrystal v Pentacyclic Core with the Appropriate Relative Stereochemistry
    • Peng, F.; Danishefsky, S. J. Toward the Total Synthesis of Maoecrystal V: an Intramolecular Diels-Alder Route to the Maoecrystal V Pentacyclic Core with the Appropriate Relative Stereochemistry Tetrahedron Lett. 2011, 52, 2104-2106 10.1016/j.tetlet.2010.11.029
    • (2011) Tetrahedron Lett. , vol.52 , pp. 2104-2106
    • Peng, F.1    Danishefsky, S.J.2
  • 194
    • 80052573501 scopus 로고    scopus 로고
    • Efficient Entry to the Hasubanan Alkaloids: First Enantioselective Total Syntheses of (-)-Hasubanonine, (-)-Runanine, (-)-Delavayine, and (+)-Periglaucine B
    • Herzon, S. B.; Calandra, N. A.; King, S. M. Efficient Entry to the Hasubanan Alkaloids: First Enantioselective Total Syntheses of (-)-Hasubanonine, (-)-Runanine, (-)-Delavayine, and (+)-Periglaucine B Angew. Chem., Int. Ed. 2011, 50, 8863-8868 10.1002/anie.201102226
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 8863-8868
    • Herzon, S.B.1    Calandra, N.A.2    King, S.M.3
  • 195
    • 84886388701 scopus 로고    scopus 로고
    • Development of Enantioselective Synthetic Routes to the Hasubanan and Acutumine Alkaloids
    • Calandra, N. A.; King, S.; Herzon, S. B. Development of Enantioselective Synthetic Routes to the Hasubanan and Acutumine Alkaloids J. Org. Chem. 2013, 78, 10031-10057 10.1021/jo401889b
    • (2013) J. Org. Chem. , vol.78 , pp. 10031-10057
    • Calandra, N.A.1    King, S.2    Herzon, S.B.3
  • 196
    • 84907788286 scopus 로고    scopus 로고
    • Substrate-Modified Functional Group Reactivity: Hasubanan and Acutumine Alkaloid Syntheses
    • King, S. M.; Herzon, S. B. Substrate-Modified Functional Group Reactivity: Hasubanan and Acutumine Alkaloid Syntheses J. Org. Chem. 2014, 79, 8937-8947 10.1021/jo501516x
    • (2014) J. Org. Chem. , vol.79 , pp. 8937-8947
    • King, S.M.1    Herzon, S.B.2
  • 197
    • 80555149224 scopus 로고    scopus 로고
    • A Short Synthesis of Nonracemic Iodocyclohexene Carboxylate Fragment for Kibdelone and Congeners
    • Endoma-Arias, M. A. A.; Hudlicky, T. A Short Synthesis of Nonracemic Iodocyclohexene Carboxylate Fragment for Kibdelone and Congeners Tetrahedron Lett. 2011, 52, 6632-6634 10.1016/j.tetlet.2011.10.005
    • (2011) Tetrahedron Lett. , vol.52 , pp. 6632-6634
    • Endoma-Arias, M.A.A.1    Hudlicky, T.2
  • 198
    • 84860646131 scopus 로고    scopus 로고
    • A Non-Photochemical Approach to the Bicyclo[3.2.0]heptane Core of Bielschowskysin
    • Farcet, J.-B.; Himmelbauer, M.; Mulzer, J. A Non-Photochemical Approach to the Bicyclo[3.2.0]heptane Core of Bielschowskysin Org. Lett. 2012, 14, 2195-2197 10.1021/ol3006419
    • (2012) Org. Lett. , vol.14 , pp. 2195-2197
    • Farcet, J.-B.1    Himmelbauer, M.2    Mulzer, J.3
  • 199
    • 84859221039 scopus 로고    scopus 로고
    • Total Synthesis and Stereochemical Reassignment of (±)-Indoxamycin B
    • Jeker, O. F.; Carreira, E. M. Total Synthesis and Stereochemical Reassignment of (±)-Indoxamycin B Angew. Chem., Int. Ed. 2012, 51, 3474-3477 10.1002/anie.201109175
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 3474-3477
    • Jeker, O.F.1    Carreira, E.M.2
  • 200
    • 84856094572 scopus 로고    scopus 로고
    • Total Synthesis of seco-Plakortolide e and (-)-ent-Plakortolide I: Absolute Configurational Revision of Natural Plakortolide i
    • Barnych, B.; Vatèle, J.-M. Total Synthesis of seco-Plakortolide E and (-)-ent-Plakortolide I: Absolute Configurational Revision of Natural Plakortolide I Org. Lett. 2012, 14, 564-567 10.1021/ol203185f
    • (2012) Org. Lett. , vol.14 , pp. 564-567
    • Barnych, B.1    Vatèle, J.-M.2
  • 201
    • 79961126600 scopus 로고    scopus 로고
    • Synthetic Studies toward the Bicyclic Peroxylactone Core of Plakortolides
    • Barnych, B.; Vatèle, J.-M. Synthetic Studies toward the Bicyclic Peroxylactone Core of Plakortolides Synlett 2011, 2011 (13) 1912-1916 10.1055/s-0030-1260959
    • (2011) Synlett , vol.2011 , Issue.13 , pp. 1912-1916
    • Barnych, B.1    Vatèle, J.-M.2
  • 202
    • 84870052961 scopus 로고    scopus 로고
    • Asymmetric Synthesis of Andavadoic Acid via Base-Catalyzed 5-exo-tet Cyclization of a β-Hydroperoxy Epoxide
    • Barnych, B.; Fenet, B.; Vatèle, J.-M. Asymmetric Synthesis of Andavadoic Acid via Base-Catalyzed 5-exo-tet Cyclization of a β-Hydroperoxy Epoxide Tetrahedron 2013, 69, 334-340 10.1016/j.tet.2012.10.022
    • (2013) Tetrahedron , vol.69 , pp. 334-340
    • Barnych, B.1    Fenet, B.2    Vatèle, J.-M.3
  • 203
    • 84944930601 scopus 로고    scopus 로고
    • Synthesis and Structural Reassignment of Plakinidone
    • Xu, Z.-J.; Tan, D.-X.; Wu, Y. Synthesis and Structural Reassignment of Plakinidone Org. Lett. 2015, 17, 5092-5095 10.1021/acs.orglett.5b02599
    • (2015) Org. Lett. , vol.17 , pp. 5092-5095
    • Xu, Z.-J.1    Tan, D.-X.2    Wu, Y.3
  • 204
    • 84922637400 scopus 로고    scopus 로고
    • Expeditious Entry to the Chamigrane Endoperoxide Family of Natural Products
    • Chen, H.-J.; Wu, Y. Expeditious Entry to the Chamigrane Endoperoxide Family of Natural Products Org. Lett. 2015, 17, 592-595 10.1021/ol503603t
    • (2015) Org. Lett. , vol.17 , pp. 592-595
    • Chen, H.-J.1    Wu, Y.2
  • 206
    • 84885622215 scopus 로고    scopus 로고
    • A Concise Enantioselective Synthesis of the Guaiane Sesquiterpene (-)-Oxyphyllol
    • Zahel, M.; Metz, P. A Concise Enantioselective Synthesis of the Guaiane Sesquiterpene (-)-Oxyphyllol Beilstein J. Org. Chem. 2013, 9, 2028-3032 10.3762/bjoc.9.239
    • (2013) Beilstein J. Org. Chem. , vol.9 , pp. 2028-3032
    • Zahel, M.1    Metz, P.2
  • 207
    • 84871855630 scopus 로고    scopus 로고
    • Strategic Redox Relay Enables A Scalable Synthesis of Ouabagenin, A Bioactive Cardenolide
    • Renata, H.; Zhou, Q.; Baran, P. S. Strategic Redox Relay Enables A Scalable Synthesis of Ouabagenin, A Bioactive Cardenolide Science 2013, 339, 59-63 10.1126/science.1230631
    • (2013) Science , vol.339 , pp. 59-63
    • Renata, H.1    Zhou, Q.2    Baran, P.S.3
  • 208
    • 84921958314 scopus 로고    scopus 로고
    • Development of a Concise Synthesis of Ouabagenin and Hydroxylated Corticosteroid Analogues
    • Renata, H.; Zhou, Q.; Dünstl, G.; Felding, J.; Merchant, R. R.; Yeh, C.-H.; Baran, P. S. Development of a Concise Synthesis of Ouabagenin and Hydroxylated Corticosteroid Analogues J. Am. Chem. Soc. 2015, 137, 1330-1340 10.1021/ja512022r
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 1330-1340
    • Renata, H.1    Zhou, Q.2    Dünstl, G.3    Felding, J.4    Merchant, R.R.5    Yeh, C.-H.6    Baran, P.S.7
  • 210
    • 84949035223 scopus 로고    scopus 로고
    • The Revised Structure of Trichodermatide A
    • Shigehisa, H.; Kikuchi, H.; Suzuki, T.; Hiroya, K. The Revised Structure of Trichodermatide A Eur. J. Org. Chem. 2015, 2015, 7670-7673 10.1002/ejoc.201501281
    • (2015) Eur. J. Org. Chem. , vol.2015 , pp. 7670-7673
    • Shigehisa, H.1    Kikuchi, H.2    Suzuki, T.3    Hiroya, K.4
  • 211
    • 84903712487 scopus 로고    scopus 로고
    • A Domino Approach to the Enantioselective Total Syntheses of Blennolide C and Gonytolide C
    • Tietze, L. F.; Jackenkroll, S.; Hierold, J.; Ma, L.; Waldecker, B. A Domino Approach to the Enantioselective Total Syntheses of Blennolide C and Gonytolide C Chem.-Eur. J. 2014, 20, 8628-8635 10.1002/chem.201402495
    • (2014) Chem. - Eur. J. , vol.20 , pp. 8628-8635
    • Tietze, L.F.1    Jackenkroll, S.2    Hierold, J.3    Ma, L.4    Waldecker, B.5
  • 212
    • 84874614791 scopus 로고    scopus 로고
    • Symmetry-Driven Synthesis of 9-Demethyl-10,15-dideoxyryanodol
    • Urabe, D.; Nagatomo, M.; Hagiwara, K.; Masuda, K.; Inoue, M. Symmetry-Driven Synthesis of 9-Demethyl-10,15-dideoxyryanodol Chem. Sci. 2013, 4, 1615-1619 10.1039/c3sc00023k
    • (2013) Chem. Sci. , vol.4 , pp. 1615-1619
    • Urabe, D.1    Nagatomo, M.2    Hagiwara, K.3    Masuda, K.4    Inoue, M.5
  • 213
    • 84907482061 scopus 로고    scopus 로고
    • A Unified Approach to ent-Atisane Diterpenes and Related Alkaloids: Synthesis of (-)-Methyl Atisenoate, (-)-Isoatisine, and the Hetidine Skeleton
    • Cherney, E. C.; Lopchuk, J. M.; Green, J. C.; Baran, P. S. A Unified Approach to ent-Atisane Diterpenes and Related Alkaloids: Synthesis of (-)-Methyl Atisenoate, (-)-Isoatisine, and the Hetidine Skeleton J. Am. Chem. Soc. 2014, 136, 12592-12595 10.1021/ja507321j
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 12592-12595
    • Cherney, E.C.1    Lopchuk, J.M.2    Green, J.C.3    Baran, P.S.4
  • 215
    • 0001541875 scopus 로고
    • Intramolecular Hydrogen Abstraction. Iodosobenzene Diacetate, an Efficient and Convenient Reagent for Alkoxy Radical Generation
    • Concepción, J. I.; Francisco, C. G.; Hernandez, R.; Salazar, J. A.; Suárez, E. Intramolecular Hydrogen Abstraction. Iodosobenzene Diacetate, an Efficient and Convenient Reagent for Alkoxy Radical Generation Tetrahedron Lett. 1984, 25, 1953-1956 10.1016/S0040-4039(01)90085-1
    • (1984) Tetrahedron Lett. , vol.25 , pp. 1953-1956
    • Concepción, J.I.1    Francisco, C.G.2    Hernandez, R.3    Salazar, J.A.4    Suárez, E.5
  • 216
    • 84898017407 scopus 로고    scopus 로고
    • Four-Step Synthesis of the Antimalarial Cardamom Peroxide via an Oxygen Stitching Strategy
    • Hu, X.; Maimone, T. J. Four-Step Synthesis of the Antimalarial Cardamom Peroxide via an Oxygen Stitching Strategy J. Am. Chem. Soc. 2014, 136, 5287-5290 10.1021/ja502208z
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 5287-5290
    • Hu, X.1    Maimone, T.J.2
  • 217
    • 84905995429 scopus 로고    scopus 로고
    • Biomimetic Synthesis of (+)-Ledene, (+)-Viridiflorol, (-)-Palustrol, (+)-Spathulenol, and Psiguadial A, C, and D via the Platform Terpene (+)-Bicyclogermacrene
    • Tran, D. N.; Cramer, N. Biomimetic Synthesis of (+)-Ledene, (+)-Viridiflorol, (-)-Palustrol, (+)-Spathulenol, and Psiguadial A, C, and D via the Platform Terpene (+)-Bicyclogermacrene Chem.-Eur. J. 2014, 20, 10654-10660 10.1002/chem.201403082
    • (2014) Chem. - Eur. J. , vol.20 , pp. 10654-10660
    • Tran, D.N.1    Cramer, N.2
  • 218
    • 79951853318 scopus 로고    scopus 로고
    • B-Carbon Elimination from Cyclobutanols: A Clean Access to Alkylrhodium Intermediates Bearing a Quaternary Stereogenic Center
    • Cramer, N.; Seiser, T. b-Carbon Elimination from Cyclobutanols: A Clean Access to Alkylrhodium Intermediates Bearing a Quaternary Stereogenic Center Synlett 2011, 2011 (4) 449-460 10.1055/s-0030-1259536
    • (2011) Synlett , vol.2011 , Issue.4 , pp. 449-460
    • Cramer, N.1    Seiser, T.2
  • 220
    • 84930226059 scopus 로고    scopus 로고
    • Total Syntheses of (-)-Mersicarpine, (-)-Scholarisine G, (+)-Melodinine E, (-)-Leuconoxine, (-)-Leuconolam, (-)-Leuconodine A, (+)-Leuconodine F, and (-)-Leuconodine C: Self-Induced Diastereomeric Anisochronism (SIDA) Phenomenon for Scholarisine G and Leuconodines A and C
    • Xu, Z.; Wang, Q.; Zhu, J. Total Syntheses of (-)-Mersicarpine, (-)-Scholarisine G, (+)-Melodinine E, (-)-Leuconoxine, (-)-Leuconolam, (-)-Leuconodine A, (+)-Leuconodine F, and (-)-Leuconodine C: Self-Induced Diastereomeric Anisochronism (SIDA) Phenomenon for Scholarisine G and Leuconodines A and C J. Am. Chem. Soc. 2015, 137, 6712-6724 10.1021/jacs.5b03619
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 6712-6724
    • Xu, Z.1    Wang, Q.2    Zhu, J.3
  • 221
    • 0034627368 scopus 로고    scopus 로고
    • Conjugate Reduction of α,β-Unsaturated Ketones using an MnIII Catalyst, Phenylsilane and Isopropyl Alcohol
    • Magnus, P.; Waring, M. J.; Scott, D. A. Conjugate Reduction of α,β-Unsaturated Ketones using an MnIII Catalyst, Phenylsilane and Isopropyl Alcohol Tetrahedron Lett. 2000, 41, 9731-9733 10.1016/S0040-4039(00)01728-7
    • (2000) Tetrahedron Lett. , vol.41 , pp. 9731-9733
    • Magnus, P.1    Waring, M.J.2    Scott, D.A.3
  • 222
    • 84939802366 scopus 로고    scopus 로고
    • Total Synthesis of Verruculogen and Fumitremorgin A Enabled by Ligand-Controlled C-H Borylation
    • Feng, Y.; Holte, D.; Zoller, J.; Umemiya, S.; Simke, L. R.; Baran, P. S. Total Synthesis of Verruculogen and Fumitremorgin A Enabled by Ligand-Controlled C-H Borylation J. Am. Chem. Soc. 2015, 137, 10160-10163 10.1021/jacs.5b07154
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 10160-10163
    • Feng, Y.1    Holte, D.2    Zoller, J.3    Umemiya, S.4    Simke, L.R.5    Baran, P.S.6
  • 223
    • 84953410922 scopus 로고    scopus 로고
    • Scalable C-H Oxidation with Copper: Synthesis of Polyoxypregnanes
    • See, Y. Y.; Herrmann, A. T.; Aihara, Y.; Baran, P. S. Scalable C-H Oxidation with Copper: Synthesis of Polyoxypregnanes J. Am. Chem. Soc. 2015, 137, 13776-13779 10.1021/jacs.5b09463
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 13776-13779
    • See, Y.Y.1    Herrmann, A.T.2    Aihara, Y.3    Baran, P.S.4
  • 224
    • 84949599624 scopus 로고    scopus 로고
    • Total Synthesis of Linckosides A and B, the Representative Starfish Polyhydroxysteroid Glycosides with Neuritogenic Activities
    • Zhu, D.; Yu, B. Total Synthesis of Linckosides A and B, the Representative Starfish Polyhydroxysteroid Glycosides with Neuritogenic Activities J. Am. Chem. Soc. 2015, 137, 15098-15101 10.1021/jacs.5b11276
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 15098-15101
    • Zhu, D.1    Yu, B.2
  • 225
    • 84946021794 scopus 로고    scopus 로고
    • Total Synthesis of Atisane-Type Diterpenoids: Application of Diels-Alder Cycloadditions of Podocarpane-Type Unmasked ortho-Benzoquinones
    • Song, L.; Zhu, G.; Liu, Y.; Liu, B.; Qin, S. Total Synthesis of Atisane-Type Diterpenoids: Application of Diels-Alder Cycloadditions of Podocarpane-Type Unmasked ortho-Benzoquinones J. Am. Chem. Soc. 2015, 137, 13706-13714 10.1021/jacs.5b08958
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 13706-13714
    • Song, L.1    Zhu, G.2    Liu, Y.3    Liu, B.4    Qin, S.5
  • 226
    • 84943201565 scopus 로고    scopus 로고
    • Ongoing Pursuit of Diterpenoid Alkaloids: A Synthetic View
    • Liu, X.-Y.; Qin, Y. Ongoing Pursuit of Diterpenoid Alkaloids: A Synthetic View Asian J. Org. Chem. 2015, 4, 1010-1019 10.1002/ajoc.201500295
    • (2015) Asian J. Org. Chem. , vol.4 , pp. 1010-1019
    • Liu, X.-Y.1    Qin, Y.2
  • 227
    • 84954270777 scopus 로고    scopus 로고
    • Utilizing an o-Quinone Methide in Asymmetric Transfer Hydrogenation: Enantioselective Synthesis of Brosimine A, Brosimine B, and Brosimacutin L
    • Keßberg, A.; Metz, P. Utilizing an o-Quinone Methide in Asymmetric Transfer Hydrogenation: Enantioselective Synthesis of Brosimine A, Brosimine B, and Brosimacutin L Angew. Chem., Int. Ed. 2016, 55, 1160-1163 10.1002/anie.201507269
    • (2016) Angew. Chem., Int. Ed. , vol.55 , pp. 1160-1163
    • Keßberg, A.1    Metz, P.2
  • 228
    • 84963500354 scopus 로고    scopus 로고
    • Nineteen-Step Total Synthesis of (+)-Phorbol
    • Kawamura, S.; Chu, H.; Felding, J.; Baran, P. S. Nineteen-Step Total Synthesis of (+)-Phorbol Nature 2016, 532, 90-93 10.1038/nature17153
    • (2016) Nature , vol.532 , pp. 90-93
    • Kawamura, S.1    Chu, H.2    Felding, J.3    Baran, P.S.4
  • 229
    • 84973139122 scopus 로고    scopus 로고
    • Total Synthesis of Rubriflordilactone B
    • Yang, P.; Yao, M.; Li, J.; Li, Y.; Li, A. Total Synthesis of Rubriflordilactone B Angew. Chem., Int. Ed. 2016, 55, 6964-6968 10.1002/anie.201601915
    • (2016) Angew. Chem., Int. Ed. , vol.55 , pp. 6964-6968
    • Yang, P.1    Yao, M.2    Li, J.3    Li, Y.4    Li, A.5
  • 230
    • 84896744848 scopus 로고    scopus 로고
    • General Approach to the Synthesis of the Chlorosulfolipids Danicalipin A, Mytilipin A, and Malhamensilipin A in Enantioenriched Form
    • Chung, W.-j.; Carlson, J. S.; Vanderwal, C. D. General Approach to the Synthesis of the Chlorosulfolipids Danicalipin A, Mytilipin A, and Malhamensilipin A in Enantioenriched Form J. Org. Chem. 2014, 79, 2226-2241 10.1021/jo5000829
    • (2014) J. Org. Chem. , vol.79 , pp. 2226-2241
    • Chung, W.-J.1    Carlson, J.S.2    Vanderwal, C.D.3
  • 232
    • 84958877706 scopus 로고    scopus 로고
    • Scalable Total Synthesis of rac-Jungermannenones B and C
    • Liu, W.; Li, H.; Cai, P.-J.; Wang, Z.; Yu, Z.-X.; Lei, X. Scalable Total Synthesis of rac-Jungermannenones B and C Angew. Chem., Int. Ed. 2016, 55, 3112-3116 10.1002/anie.201511659
    • (2016) Angew. Chem., Int. Ed. , vol.55 , pp. 3112-3116
    • Liu, W.1    Li, H.2    Cai, P.-J.3    Wang, Z.4    Yu, Z.-X.5    Lei, X.6
  • 233
    • 70349158042 scopus 로고    scopus 로고
    • Organic Radical Reactions Associated with Nitrogen Monoxide
    • Hartung, J. Organic Radical Reactions Associated with Nitrogen Monoxide Chem. Rev. 2009, 109, 4500-4517 10.1021/cr900085j
    • (2009) Chem. Rev. , vol.109 , pp. 4500-4517
    • Hartung, J.1
  • 234
    • 0343395661 scopus 로고
    • Cobalt-Catalyzed Reaction of Nitric Oxide with Aryl-Substituted Olefins in the Presence of Tetrahydroborate Ion
    • Okamoto, T.; Kobayashi, K.; Oka, S.; Tanimoto, S. Cobalt-Catalyzed Reaction of Nitric Oxide with Aryl-Substituted Olefins in the Presence of Tetrahydroborate Ion J. Org. Chem. 1987, 52, 5089-5092 10.1021/jo00232a005
    • (1987) J. Org. Chem. , vol.52 , pp. 5089-5092
    • Okamoto, T.1    Kobayashi, K.2    Oka, S.3    Tanimoto, S.4
  • 236
    • 0003166969 scopus 로고
    • Nitrosation of α,β-Unsaturated Carboxamide with Nitric Oxide and Triethylsilane Catalyzed by Cobalt(II) Complex
    • Kato, K.; Mukaiyama, T. Nitrosation of α,β-Unsaturated Carboxamide with Nitric Oxide and Triethylsilane Catalyzed by Cobalt(II) Complex Chem. Lett. 1990, 19, 1395-1398 10.1246/cl.1990.1395
    • (1990) Chem. Lett. , vol.19 , pp. 1395-1398
    • Kato, K.1    Mukaiyama, T.2
  • 237
    • 2742579804 scopus 로고
    • A Novel Method for the Preparation of 2-Hydroxyiminocarboxylic Acid Esters. Cobalt(II) Catalyzed α-Oximation of α,β-Unsaturated Esters with Butyl Nitrite and Phenylsilane
    • Kato, K.; Mukaiyama, T. A Novel Method for the Preparation of 2-Hydroxyiminocarboxylic Acid Esters. Cobalt(II) Catalyzed α-Oximation of α,β-Unsaturated Esters with Butyl Nitrite and Phenylsilane Chem. Lett. 1990, 19, 1917-1920 10.1246/cl.1990.1917
    • (1990) Chem. Lett. , vol.19 , pp. 1917-1920
    • Kato, K.1    Mukaiyama, T.2
  • 238
    • 0013217149 scopus 로고
    • A Novel and Efficient Method for the Preparation of α-Hydroxyimino Carbonyl Compounds from α,β-Unsaturated Carbonyl Compounds with Butyl Nitrite and Phenylsilane Catalyzed by a Cobalt(II) Complex
    • Kato, K.; Mukaiyama, T. A Novel and Efficient Method for the Preparation of α-Hydroxyimino Carbonyl Compounds from α,β-Unsaturated Carbonyl Compounds with Butyl Nitrite and Phenylsilane Catalyzed by a Cobalt(II) Complex Bull. Chem. Soc. Jpn. 1991, 64, 2948-2953 10.1246/bcsj.64.2948
    • (1991) Bull. Chem. Soc. Jpn. , vol.64 , pp. 2948-2953
    • Kato, K.1    Mukaiyama, T.2
  • 239
    • 2742609763 scopus 로고
    • Iron(III) Complex Catalyzed Nitrosation of Terminal and 1,2-Disubstituted Olefins with Butyl Nitrite and Phenylsilane
    • Kato, K.; Mukaiyama, T. Iron(III) Complex Catalyzed Nitrosation of Terminal and 1,2-Disubstituted Olefins with Butyl Nitrite and Phenylsilane Chem. Lett. 1992, 21, 1137-1140 10.1246/cl.1992.1137
    • (1992) Chem. Lett. , vol.21 , pp. 1137-1140
    • Kato, K.1    Mukaiyama, T.2
  • 240
    • 33947479652 scopus 로고
    • The Synthesis of Nitrosoalkane Dimers
    • Emmons, W. D. The Synthesis of Nitrosoalkane Dimers J. Am. Chem. Soc. 1957, 79, 6522-6524 10.1021/ja01581a043
    • (1957) J. Am. Chem. Soc. , vol.79 , pp. 6522-6524
    • Emmons, W.D.1
  • 241
    • 3543110157 scopus 로고    scopus 로고
    • Preparations of C-Nitroso Compounds
    • Gowenlock, B. G.; Richter-Addo, G. B. Preparations of C-Nitroso Compounds Chem. Rev. 2004, 104, 3315-3340 10.1021/cr030450k
    • (2004) Chem. Rev. , vol.104 , pp. 3315-3340
    • Gowenlock, B.G.1    Richter-Addo, G.B.2
  • 242
    • 0030232167 scopus 로고    scopus 로고
    • Nitrosation and Nitration of Olefins Using Nitrogen Monoxide
    • Hata, E.; Kato, K.; Yamada, T.; Mukaiyama, T. Nitrosation and Nitration of Olefins Using Nitrogen Monoxide Yuki Gosei Kagaku Kyokaishi 1996, 54, 728-739 10.5059/yukigoseikyokaishi.54.728
    • (1996) Yuki Gosei Kagaku Kyokaishi , vol.54 , pp. 728-739
    • Hata, E.1    Kato, K.2    Yamada, T.3    Mukaiyama, T.4
  • 243
    • 0002685107 scopus 로고    scopus 로고
    • A Synthesis of Oximes from Olefins by Cobalt(II) Porphyrin-Catalyzed Reduction-Nitrosation
    • Sugamoto, K.; Hamasuna, Y.; Matsushita, Y.-i.; Matsui, T. A Synthesis of Oximes from Olefins by Cobalt(II) Porphyrin-Catalyzed Reduction-Nitrosation Synlett 1998, 1998 (11) 1270-1272 10.1055/s-1998-1933
    • (1998) Synlett , vol.1998 , Issue.11 , pp. 1270-1272
    • Sugamoto, K.1    Hamasuna, Y.2    Matsushita, Y.-I.3    Matsui, T.4
  • 245
    • 84889634682 scopus 로고    scopus 로고
    • Iron Catalysed Nitrosation of Olefins to Oximes
    • Ray, R.; Chowdhury, A. D.; Maiti, D.; Lahiri, G. K. Iron Catalysed Nitrosation of Olefins to Oximes Dalton Trans. 2014, 43, 38-41 10.1039/C3DT51764K
    • (2014) Dalton Trans. , vol.43 , pp. 38-41
    • Ray, R.1    Chowdhury, A.D.2    Maiti, D.3    Lahiri, G.K.4
  • 246
    • 0028260133 scopus 로고
    • Solvent Effect in Pericyclic Reactions. IX. the Ene Reaction
    • Desimoni, G.; Faita, G.; Righetti, P. P.; Sfulcini, A.; Tsyganov, D. Solvent Effect in Pericyclic Reactions. IX. The Ene Reaction Tetrahedron 1994, 50, 1821-1832 10.1016/S0040-4020(01)80854-1
    • (1994) Tetrahedron , vol.50 , pp. 1821-1832
    • Desimoni, G.1    Faita, G.2    Righetti, P.P.3    Sfulcini, A.4    Tsyganov, D.5
  • 247
    • 0005539434 scopus 로고
    • Ene Reactions of Conjugated Dienes. 2. Dependence of Rate on Degree of Hydrogen Removed and s-Cis or s-Trans Diene Character
    • Jacobson, B. M.; Arvanitis, G. M.; Eliasen, C. A.; Mitelman, R. Ene Reactions of Conjugated Dienes. 2. Dependence of Rate on Degree of Hydrogen Removed and s-Cis or s-Trans Diene Character J. Org. Chem. 1985, 50, 194-201 10.1021/jo00202a011
    • (1985) J. Org. Chem. , vol.50 , pp. 194-201
    • Jacobson, B.M.1    Arvanitis, G.M.2    Eliasen, C.A.3    Mitelman, R.4
  • 248
    • 0023936049 scopus 로고
    • Synthesis of Adamantane Derivatives by Bridgehead Radical Addition to Electron-Deficient Unsaturated Bonds
    • Ohno, M.; Ishizaki, K.; Eguchi, S. Synthesis Of Adamantane Derivatives by Bridgehead Radical Addition to Electron-Deficient Unsaturated Bonds J. Org. Chem. 1988, 53, 1285-1288 10.1021/jo00241a030
    • (1988) J. Org. Chem. , vol.53 , pp. 1285-1288
    • Ohno, M.1    Ishizaki, K.2    Eguchi, S.3
  • 249
    • 84869193189 scopus 로고    scopus 로고
    • 3)-H Bonds Using N-Hydroxyphthalimide and Dialkyl Azodicarboxylate
    • 3)-H Bonds Using N-Hydroxyphthalimide and Dialkyl Azodicarboxylate J. Org. Chem. 2012, 77, 9959-9969 10.1021/jo301840e
    • (2012) J. Org. Chem. , vol.77 , pp. 9959-9969
    • Amaoka, Y.1    Kamijo, S.2    Hoshikawa, T.3    Inoue, M.4
  • 250
    • 0033532193 scopus 로고    scopus 로고
    • Electrophilic Amination of Racemic and Non-Racemic Allenyltitaniums. One-Pot Synthesis of α-Hydrazinoalkynes from Propargylic Alcohol Derivatives
    • An, D. K.; Hirakawa, H.; Okamoto, S.; Sato, F. Electrophilic Amination of Racemic and Non-Racemic Allenyltitaniums. One-Pot Synthesis of α-Hydrazinoalkynes from Propargylic Alcohol Derivatives Tetrahedron Lett. 1999, 40, 3737-3740 10.1016/S0040-4039(99)00584-5
    • (1999) Tetrahedron Lett. , vol.40 , pp. 3737-3740
    • An, D.K.1    Hirakawa, H.2    Okamoto, S.3    Sato, F.4
  • 251
    • 0032506574 scopus 로고    scopus 로고
    • Electrophilic Amination of Organozinc Halides
    • Velarde-Ortiz, R.; Guijarro, A.; Rieke, R. D. Electrophilic Amination of Organozinc Halides Tetrahedron Lett. 1998, 39, 9157-9160 10.1016/S0040-4039(98)02108-X
    • (1998) Tetrahedron Lett. , vol.39 , pp. 9157-9160
    • Velarde-Ortiz, R.1    Guijarro, A.2    Rieke, R.D.3
  • 252
    • 2442590635 scopus 로고    scopus 로고
    • Convenient Synthesis of Alkylhydrazides by the Cobalt-Catalyzed Hydrohydrazination Reaction of Olefins and Azodicarboxylates
    • Waser, J.; Carreira, E. M. Convenient Synthesis of Alkylhydrazides by the Cobalt-Catalyzed Hydrohydrazination Reaction of Olefins and Azodicarboxylates J. Am. Chem. Soc. 2004, 126, 5676-5677 10.1021/ja048698u
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 5676-5677
    • Waser, J.1    Carreira, E.M.2
  • 253
    • 84903582565 scopus 로고    scopus 로고
    • Azodicarboxylates: Synthesis and Functionalization of Organic Compounds
    • Zhirov, A. M.; Aksenov, A. V. Azodicarboxylates: Synthesis and Functionalization of Organic Compounds Russ. Chem. Rev. 2014, 83, 502-522 10.1070/RC2014v083n06ABEH004419
    • (2014) Russ. Chem. Rev. , vol.83 , pp. 502-522
    • Zhirov, A.M.1    Aksenov, A.V.2
  • 254
    • 0030976836 scopus 로고    scopus 로고
    • A Versatile Cobalt(II)-Schiff Base Catalyzed Oxidation of Organic Substrates with Dioxygen: Scope and Mechanism
    • Punniyamurthy, T.; Bhatia, B.; Reddy, M. M.; Maikap, G. C.; Iqbal, J. A Versatile Cobalt(II)-Schiff Base Catalyzed Oxidation of Organic Substrates with Dioxygen: Scope and Mechanism Tetrahedron 1997, 53, 7649-7670 10.1016/S0040-4020(97)00432-8
    • (1997) Tetrahedron , vol.53 , pp. 7649-7670
    • Punniyamurthy, T.1    Bhatia, B.2    Reddy, M.M.3    Maikap, G.C.4    Iqbal, J.5
  • 255
    • 4544298061 scopus 로고    scopus 로고
    • Catalytic Hydrohydrazination of a Wide Range of Alkenes with a Simple Mn Complex
    • Waser, J.; Carreira, E. M. Catalytic Hydrohydrazination of a Wide Range of Alkenes with a Simple Mn Complex Angew. Chem., Int. Ed. 2004, 43, 4099-4102 10.1002/anie.200460811
    • (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 4099-4102
    • Waser, J.1    Carreira, E.M.2
  • 256
    • 25444458879 scopus 로고    scopus 로고
    • Cobalt-Catalyzed Hydrohydrazination of Dienes and Enynes: Access to Allylic and Propargylic Hydrazides
    • Waser, J.; González-Gómez, J. C.; Nambu, H.; Huber, P.; Carreira, E. M. Cobalt-Catalyzed Hydrohydrazination of Dienes and Enynes: Access to Allylic and Propargylic Hydrazides Org. Lett. 2005, 7, 4249-4252 10.1021/ol0517473
    • (2005) Org. Lett. , vol.7 , pp. 4249-4252
    • Waser, J.1    González-Gómez, J.C.2    Nambu, H.3    Huber, P.4    Carreira, E.M.5
  • 257
    • 19444388114 scopus 로고    scopus 로고
    • Stereoselective a-Hydrazination of a,b-Unsaturated Carboxylates Catalyzed by Manganese(III) Complex with Dialkylazodicarboxylate and Phenylsilane
    • Sato, M.; Gunji, Y.; Ikeno, T.; Yamada, T. Stereoselective a-Hydrazination of a,b-Unsaturated Carboxylates Catalyzed by Manganese(III) Complex with Dialkylazodicarboxylate and Phenylsilane Chem. Lett. 2005, 34, 316-317 10.1246/cl.2005.316
    • (2005) Chem. Lett. , vol.34 , pp. 316-317
    • Sato, M.1    Gunji, Y.2    Ikeno, T.3    Yamada, T.4
  • 258
    • 80052249648 scopus 로고    scopus 로고
    • Scalable Synthesis of 1-Bicyclo[1.1.1]pentylamine via a Hydrohydrazination Reaction
    • Bunker, K. D.; Sach, N. W.; Huang, Q.; Richardson, P. F. Scalable Synthesis of 1-Bicyclo[1.1.1]pentylamine via a Hydrohydrazination Reaction Org. Lett. 2011, 13, 4746-4748 10.1021/ol201883z
    • (2011) Org. Lett. , vol.13 , pp. 4746-4748
    • Bunker, K.D.1    Sach, N.W.2    Huang, Q.3    Richardson, P.F.4
  • 260
    • 84953395586 scopus 로고    scopus 로고
    • Fe-Catalyzed Olefin Hydroamination with Diazo Compounds for Hydrazone Synthesis
    • Zheng, J.; Qi, J.; Cui, S. Fe-Catalyzed Olefin Hydroamination with Diazo Compounds for Hydrazone Synthesis Org. Lett. 2016, 18, 128-131 10.1021/acs.orglett.5b03317
    • (2016) Org. Lett. , vol.18 , pp. 128-131
    • Zheng, J.1    Qi, J.2    Cui, S.3
  • 261
    • 80053323246 scopus 로고    scopus 로고
    • New Electrophilic Addition of α-Diazoesters with Ketones for Enantioselective C-N Bond Formation
    • Li, W.; Liu, X.; Hao, X.; Hu, X.; Chu, Y.; Cao, W.; Qin, S.; Hu, C.; Lin, L.; Feng, X. New Electrophilic Addition of α-Diazoesters with Ketones for Enantioselective C-N Bond Formation J. Am. Chem. Soc. 2011, 133, 15268 10.1021/ja2056159
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 15268
    • Li, W.1    Liu, X.2    Hao, X.3    Hu, X.4    Chu, Y.5    Cao, W.6    Qin, S.7    Hu, C.8    Lin, L.9    Feng, X.10
  • 262
    • 84942820533 scopus 로고    scopus 로고
    • Activation of α-Diazocarbonyls by Organic Catalysts: Diazo Group Acting as a Strong N-Terminal Electrophile
    • Li, L.; Chen, J.-J.; Li, Y.-J.; Bu, X.-B.; Liu, Q.; Zhao, Y.-L. Activation of α-Diazocarbonyls by Organic Catalysts: Diazo Group Acting as a Strong N-Terminal Electrophile Angew. Chem., Int. Ed. 2015, 54, 12107-12111 10.1002/anie.201505064
    • (2015) Angew. Chem., Int. Ed. , vol.54 , pp. 12107-12111
    • Li, L.1    Chen, J.-J.2    Li, Y.-J.3    Bu, X.-B.4    Liu, Q.5    Zhao, Y.-L.6
  • 263
    • 84942279542 scopus 로고    scopus 로고
    • Modern Organic Synthesis with α-Diazocarbonyl Compounds
    • Ford, A.; Miel, H.; Ring, A.; Slattery, C. N.; Maguire, A. R.; McKervey, M. A. Modern Organic Synthesis with α-Diazocarbonyl Compounds Chem. Rev. 2015, 115, 9981-10080 10.1021/acs.chemrev.5b00121
    • (2015) Chem. Rev. , vol.115 , pp. 9981-10080
    • Ford, A.1    Miel, H.2    Ring, A.3    Slattery, C.N.4    Maguire, A.R.5    McKervey, M.A.6
  • 266
    • 84941923105 scopus 로고    scopus 로고
    • Fe-Catalyzed Reductive Coupling of Unactivated Alkenes with β-Nitroalkenes
    • Zheng, J.; Wang, D.; Cui, S. Fe-Catalyzed Reductive Coupling of Unactivated Alkenes with β-Nitroalkenes Org. Lett. 2015, 17, 4572-4575 10.1021/acs.orglett.5b02294
    • (2015) Org. Lett. , vol.17 , pp. 4572-4575
    • Zheng, J.1    Wang, D.2    Cui, S.3
  • 267
    • 20444468454 scopus 로고    scopus 로고
    • Cobalt-Catalyzed Hydroazidation of Olefins: Convenient Access to Alkyl Azides
    • Waser, J.; Nambu, H.; Carreira, E. M. Cobalt-Catalyzed Hydroazidation of Olefins: Convenient Access to Alkyl Azides J. Am. Chem. Soc. 2005, 127, 8294-8295 10.1021/ja052164r
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 8294-8295
    • Waser, J.1    Nambu, H.2    Carreira, E.M.3
  • 268
    • 37549065466 scopus 로고    scopus 로고
    • Cobalt-Catalyzed Synthesis of Tertiary Azides from α,α-Disubstituted Olefins under Mild Conditions Using Commercially Available Reagents
    • Gaspar, B.; Waser, J.; Carreira, E. Cobalt-Catalyzed Synthesis of Tertiary Azides from α,α-Disubstituted Olefins under Mild Conditions Using Commercially Available Reagents Synthesis 2007, 2007, 3839-3845 10.1055/s-2007-1000817
    • (2007) Synthesis , vol.2007 , pp. 3839-3845
    • Gaspar, B.1    Waser, J.2    Carreira, E.3
  • 269
    • 0000096835 scopus 로고    scopus 로고
    • Click Chemistry: Diverse Chemical Function from a Few Good Reactions
    • Kolb, H. C.; Finn, M. G.; Sharpless, K. B. Click Chemistry: Diverse Chemical Function from a Few Good Reactions Angew. Chem., Int. Ed. 2001, 40, 2004-2021 10.1002/1521-3773(20010601)40:11<2004::AID-ANIE2004>3.0.CO;2-5
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 2004-2021
    • Kolb, H.C.1    Finn, M.G.2    Sharpless, K.B.3
  • 270
    • 84907486667 scopus 로고    scopus 로고
    • Catalytic Hydroamination of Unactivated Olefins Using a Co Catalyst for Complex Molecule Synthesis
    • Shigehisa, H.; Koseki, N.; Shimizu, N.; Fujisawa, M.; Niitsu, M.; Hiroya, K. Catalytic Hydroamination of Unactivated Olefins Using a Co Catalyst for Complex Molecule Synthesis J. Am. Chem. Soc. 2014, 136, 13534-13537 10.1021/ja507295u
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 13534-13537
    • Shigehisa, H.1    Koseki, N.2    Shimizu, N.3    Fujisawa, M.4    Niitsu, M.5    Hiroya, K.6
  • 271
    • 84886264618 scopus 로고    scopus 로고
    • Cobalt-Catalyzed Hydrofluorination of Unactivated Olefins: A Radical Approach of Fluorine Transfer
    • Shigehisa, H.; Nishi, E.; Fujisawa, M.; Hiroya, K. Cobalt-Catalyzed Hydrofluorination of Unactivated Olefins: A Radical Approach of Fluorine Transfer Org. Lett. 2013, 15, 5158-5161 10.1021/ol402696h
    • (2013) Org. Lett. , vol.15 , pp. 5158-5161
    • Shigehisa, H.1    Nishi, E.2    Fujisawa, M.3    Hiroya, K.4
  • 272
    • 37049136496 scopus 로고
    • Abnormal Addition of Free Radicals to Sterically Hindered Nitrosobenzenes
    • Hosogai, T.; Inamoto, N.; Okazaki, R. Abnormal Addition of Free Radicals to Sterically Hindered Nitrosobenzenes J. Chem. Soc. C 1971, 3399-3401 10.1039/j39710003399
    • (1971) J. Chem. Soc. C , pp. 3399-3401
    • Hosogai, T.1    Inamoto, N.2    Okazaki, R.3
  • 273
    • 0001456565 scopus 로고
    • Methods for the Synthesis of Chiral Hindered Amines
    • Corey, E. J.; Gross, A. W. Methods for the Synthesis of Chiral Hindered Amines J. Org. Chem. 1985, 50, 5391-5393 10.1021/jo00225a082
    • (1985) J. Org. Chem. , vol.50 , pp. 5391-5393
    • Corey, E.J.1    Gross, A.W.2
  • 274
    • 33751025828 scopus 로고
    • Spin Trapping
    • Janzen, E. G. Spin Trapping Acc. Chem. Res. 1971, 4, 31-40 10.1021/ar50037a005
    • (1971) Acc. Chem. Res. , vol.4 , pp. 31-40
    • Janzen, E.G.1
  • 275
    • 0004881197 scopus 로고
    • Reactions of Nitro Compounds with 1-Cyano-1-methylethyl Radicals Produced by the Decomposition of α,α′-Azobisisobutyronitrile
    • Inamoto, N.; Simamura, O. Reactions of Nitro Compounds with 1-Cyano-1-methylethyl Radicals Produced by the Decomposition of α,α′-Azobisisobutyronitrile J. Org. Chem. 1958, 23, 408-410 10.1021/jo01097a022
    • (1958) J. Org. Chem. , vol.23 , pp. 408-410
    • Inamoto, N.1    Simamura, O.2
  • 276
    • 37049170516 scopus 로고
    • Properties and Reactions of Free Alkyl Radicals in Solution. Part VII. Reactions with Quinone Imides, Nitric Oxide, and Nitroso-Compounds
    • Gingras, B. A.; Waters, W. A. Properties and Reactions of Free Alkyl Radicals in Solution. Part VII. Reactions with Quinone Imides, Nitric Oxide, and Nitroso-Compounds J. Chem. Soc. 1954, 1920-1924 10.1039/jr9540001920
    • (1954) J. Chem. Soc. , pp. 1920-1924
    • Gingras, B.A.1    Waters, W.A.2
  • 277
    • 84977871252 scopus 로고    scopus 로고
    • Amine-bis(phenolate) Iron(III)-Catalyzed Formal Hydroamination of Olefins
    • Zhu, K.; Shaver, M. P.; Thomas, S. P. Amine-bis(phenolate) Iron(III)-Catalyzed Formal Hydroamination of Olefins Chem.-Asian J. 2016, 11, 977-980 10.1002/asia.201501098
    • (2016) Chem. - Asian J. , vol.11 , pp. 977-980
    • Zhu, K.1    Shaver, M.P.2    Thomas, S.P.3
  • 278
    • 84966699048 scopus 로고    scopus 로고
    • Chemoselective Nitro Reduction and Hydroamination using a Single Iron Catalyst
    • Zhu, K.; Shaver, M. P.; Thomas, S. P. Chemoselective Nitro Reduction and Hydroamination using a Single Iron Catalyst Chem. Sci. 2016, 7, 3031-3035 10.1039/C5SC04471E
    • (2016) Chem. Sci. , vol.7 , pp. 3031-3035
    • Zhu, K.1    Shaver, M.P.2    Thomas, S.P.3
  • 279
    • 1542525068 scopus 로고    scopus 로고
    • Palladium- and Cobalt-Mediated Cyclisations of Halo-Polyenes: A Comparative Study
    • Ali, A.; Gill, G. B.; Pattenden, G.; Roan, G. A.; Kam, T.-S. Palladium- and Cobalt-Mediated Cyclisations of Halo-Polyenes: a Comparative Study J. Chem. Soc., Perkin Trans. 1 1996, 1081-1093 10.1039/p19960001081
    • (1996) J. Chem. Soc., Perkin Trans. 1 , pp. 1081-1093
    • Ali, A.1    Gill, G.B.2    Pattenden, G.3    Roan, G.A.4    Kam, T.-S.5
  • 280
    • 0001601724 scopus 로고
    • The Reaction of Bis(dimethylglyoximato) (pyridine)cobalt(I), Cobaloxime(I), with 2-(Allyloxy)ethyl Halides and the Photolysis of the Resulting Organo-cobaloximes
    • Okabe, M.; Tada, M. The Reaction of Bis(dimethylglyoximato) (pyridine)cobalt(I), Cobaloxime(I), with 2-(Allyloxy)ethyl Halides and the Photolysis of the Resulting Organo-cobaloximes Bull. Chem. Soc. Jpn. 1982, 55, 1498-1503 10.1246/bcsj.55.1498
    • (1982) Bull. Chem. Soc. Jpn. , vol.55 , pp. 1498-1503
    • Okabe, M.1    Tada, M.2
  • 281
    • 37049087280 scopus 로고
    • Cobalt-Mediated Cyclization of Amino Acid Derivatives. Application to the Kainoids
    • Baldwin, J. E.; Li, C.-S. Cobalt-Mediated Cyclization of Amino Acid Derivatives. Application to the Kainoids J. Chem. Soc., Chem. Commun. 1987, 166-168 10.1039/c39870000166
    • (1987) J. Chem. Soc., Chem. Commun. , pp. 166-168
    • Baldwin, J.E.1    Li, C.-S.2
  • 282
    • 0025939924 scopus 로고
    • Cobaloxime-Catalyzed Radical Alkyl-Styryl Cross Couplings
    • Branchaud, B. P.; Detlefsen, W. D. Cobaloxime-Catalyzed Radical Alkyl-Styryl Cross Couplings Tetrahedron Lett. 1991, 32, 6273-6276 10.1016/0040-4039(91)80145-V
    • (1991) Tetrahedron Lett. , vol.32 , pp. 6273-6276
    • Branchaud, B.P.1    Detlefsen, W.D.2
  • 283
    • 0025277261 scopus 로고
    • Vitamin B129 a Catalyst in the Synthesis of Prostaglandins
    • Busato, S.; Tinembart, O.; Zhang, Z.-d.; Scheffold, R. Vitamin B129 a Catalyst in the Synthesis Of Prostaglandins Tetrahedron 1990, 46, 3155-3166 10.1016/S0040-4020(01)85455-7
    • (1990) Tetrahedron , vol.46 , pp. 3155-3166
    • Busato, S.1    Tinembart, O.2    Zhang, Z.-D.3    Scheffold, R.4
  • 284
    • 0001300267 scopus 로고
    • Cobaloxime-Catalyzed Hydroperfluoroalkylation of Electron-Deficient Alkenes with Perfluoroalkyl Halides: Reaction and Mechanism
    • Hu, C.; Qiu, Y. Cobaloxime-Catalyzed Hydroperfluoroalkylation of Electron-Deficient Alkenes with Perfluoroalkyl Halides: Reaction and Mechanism J. Org. Chem. 1992, 57, 3339-3342 10.1021/jo00038a022
    • (1992) J. Org. Chem. , vol.57 , pp. 3339-3342
    • Hu, C.1    Qiu, Y.2
  • 285
    • 0000995034 scopus 로고
    • Indirect Electrochemical Radical Cyclization of Bromo Acetals by the Combined Use of Cobaloxime and Sacrificial Electrode
    • Inokuchi, T.; Kawafuchi, H.; Aoki, K.; Yoshida, A.; Torii, S. Indirect Electrochemical Radical Cyclization of Bromo Acetals by the Combined Use of Cobaloxime and Sacrificial Electrode Bull. Chem. Soc. Jpn. 1994, 67, 595-598 10.1246/bcsj.67.595
    • (1994) Bull. Chem. Soc. Jpn. , vol.67 , pp. 595-598
    • Inokuchi, T.1    Kawafuchi, H.2    Aoki, K.3    Yoshida, A.4    Torii, S.5
  • 286
    • 84923787935 scopus 로고
    • Living Radical Polymerization of Acrylates by Organocobalt Porphyrin Complexes
    • Wayland, B. B.; Poszmik, G.; Mukerjee, S. L.; Fryd, M. Living Radical Polymerization of Acrylates by Organocobalt Porphyrin Complexes J. Am. Chem. Soc. 1994, 116, 7943-7944 10.1021/ja00096a080
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 7943-7944
    • Wayland, B.B.1    Poszmik, G.2    Mukerjee, S.L.3    Fryd, M.4
  • 290
    • 56249095471 scopus 로고    scopus 로고
    • Initiating radical cyclizations by H• transfer from transition metals
    • Hartung, J.; Pulling, M. E.; Smith, D. M.; Yang, D. X.; Norton, J. R. Initiating radical cyclizations by H• transfer from transition metals Tetrahedron 2008, 64, 11822-11830 10.1016/j.tet.2008.10.030
    • (2008) Tetrahedron , vol.64 , pp. 11822-11830
    • Hartung, J.1    Pulling, M.E.2    Smith, D.M.3    Yang, D.X.4    Norton, J.R.5
  • 291
    • 84921957667 scopus 로고    scopus 로고
    • Direct generation of oxygen-stabilized radicals by H∗ transfer from transition metal hydrides
    • Kuo, J. L.; Hartung, J.; Han, A.; Norton, J. R. Direct generation of oxygen-stabilized radicals by H∗ transfer from transition metal hydrides J. Am. Chem. Soc. 2015, 137, 1036-1039 10.1021/ja511883b
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 1036-1039
    • Kuo, J.L.1    Hartung, J.2    Han, A.3    Norton, J.R.4
  • 292
    • 84896778196 scopus 로고    scopus 로고
    • Effect of Double-Bond Substituents on the Rate of Cyclization of α-Carbomethoxyhex-5-enyl Radicals
    • Han, A.; Spataru, T.; Hartung, J., Jr.; Li, G.; Norton, J. R. Effect of Double-Bond Substituents on the Rate of Cyclization of α-Carbomethoxyhex-5-enyl Radicals J. Org. Chem. 2014, 79, 1938-1946 10.1021/jo402499w
    • (2014) J. Org. Chem. , vol.79 , pp. 1938-1946
    • Han, A.1    Spataru, T.2    Hartung, Jr.J.3    Li, G.4    Norton, J.R.5
  • 293
    • 0033751346 scopus 로고    scopus 로고
    • 3· of Chain Transfer during the Free Radical Polymerization of Methyl Methacrylate
    • 3· of Chain Transfer during the Free Radical Polymerization of Methyl Methacrylate Macromolecules 2000, 33, 2790-2792 10.1021/ma9914523
    • (2000) Macromolecules , vol.33 , pp. 2790-2792
    • Abramo, G.P.1    Norton, J.R.2
  • 294
    • 0346058167 scopus 로고    scopus 로고
    • Inverse Temperature Dependence of Chain Transfer Rate Constant for a Chromium Metalloradical in Polymerization of MMA
    • Tang, L.; Norton, J. R.; Edwards, J. C. Inverse Temperature Dependence of Chain Transfer Rate Constant for a Chromium Metalloradical in Polymerization of MMA Macromolecules 2003, 36, 9716-9720 10.1021/ma0349736
    • (2003) Macromolecules , vol.36 , pp. 9716-9720
    • Tang, L.1    Norton, J.R.2    Edwards, J.C.3
  • 296
    • 0442279550 scopus 로고    scopus 로고
    • Effect of Steric Congestion on the Activity of Chromium and Molybdenum Metalloradicals as Chain Transfer Catalysts during MMA Polymerization
    • Tang, L.; Norton, J. R. Effect of Steric Congestion on the Activity of Chromium and Molybdenum Metalloradicals as Chain Transfer Catalysts during MMA Polymerization Macromolecules 2004, 37, 241-243 10.1021/ma035612t
    • (2004) Macromolecules , vol.37 , pp. 241-243
    • Tang, L.1    Norton, J.R.2
  • 297
    • 33846125248 scopus 로고    scopus 로고
    • Factors Affecting the Apparent Chain Transfer Rate Constants of Chromium Metalloradicals: Mechanistic Implications
    • Tang, L.; Norton, J. R. Factors Affecting the Apparent Chain Transfer Rate Constants of Chromium Metalloradicals: Mechanistic Implications Macromolecules 2006, 39, 8229-8235 10.1021/ma061574c
    • (2006) Macromolecules , vol.39 , pp. 8229-8235
    • Tang, L.1    Norton, J.R.2
  • 298
    • 33846144200 scopus 로고    scopus 로고
    • 3H to Various Olefins: Influence of Olefin Structure
    • 3H to Various Olefins: Influence of Olefin Structure J. Am. Chem. Soc. 2007, 129, 234-240 10.1021/ja066325i
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 234-240
    • Choi, J.1    Tang, L.2    Norton, J.R.3
  • 299
    • 33846611139 scopus 로고    scopus 로고
    • Tin-Free and Catalytic Radical Cyclizations
    • Smith, D. M.; Pulling, M. E.; Norton, J. R. Tin-Free and Catalytic Radical Cyclizations J. Am. Chem. Soc. 2007, 129, 770-771 10.1021/ja0673276
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 770-771
    • Smith, D.M.1    Pulling, M.E.2    Norton, J.R.3
  • 302
    • 84919346981 scopus 로고    scopus 로고
    • The Reaction of Cobaloximes with Hydrogen: Products and Thermodynamics
    • Estes, D. P.; Grills, D. C.; Norton, J. R. The Reaction of Cobaloximes with Hydrogen: Products and Thermodynamics J. Am. Chem. Soc. 2014, 136, 17362-17365 10.1021/ja508200g
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 17362-17365
    • Estes, D.P.1    Grills, D.C.2    Norton, J.R.3
  • 303
    • 0000020896 scopus 로고
    • Regio- and Stereo-Selectivity of Alkenyl Radical Ring Closure: A Theoretical Study
    • Beckwith, A. L. J.; Schiesser, C. H. Regio- and Stereo-Selectivity of Alkenyl Radical Ring Closure: A Theoretical Study Tetrahedron 1985, 41, 3925-3941 10.1016/S0040-4020(01)97174-1
    • (1985) Tetrahedron , vol.41 , pp. 3925-3941
    • Beckwith, A.L.J.1    Schiesser, C.H.2
  • 304
    • 33845282341 scopus 로고
    • A Force-Field Model for Intramolecular Radical Additions
    • Spellmeyer, D. C.; Houk, K. N. A Force-Field Model for Intramolecular Radical Additions J. Org. Chem. 1987, 52, 959-974 10.1021/jo00382a001
    • (1987) J. Org. Chem. , vol.52 , pp. 959-974
    • Spellmeyer, D.C.1    Houk, K.N.2
  • 305
    • 0001330527 scopus 로고
    • Free Radical Type Addition of Toluenesulfonyl Cyanide to Unsaturated Hydrocarbons
    • Fang, J.-M.; Chen, M.-Y. Free Radical Type Addition of Toluenesulfonyl Cyanide to Unsaturated Hydrocarbons Tetrahedron Lett. 1987, 28, 2853-2856 10.1016/S0040-4039(00)96226-9
    • (1987) Tetrahedron Lett. , vol.28 , pp. 2853-2856
    • Fang, J.-M.1    Chen, M.-Y.2
  • 306
    • 0025845017 scopus 로고
    • Radical Nitrile Transfer with Methanesulfonyl Cyanide or p-Toluenesulfonyl Cyanide to Carbon Radicals Generated from the Acyl Derivatives of N-Hydroxy-2-Thiopyridone
    • Barton, D. H. R.; Jaszberenyi, J. Cs.; Theodorakis, E. A. Radical Nitrile Transfer with Methanesulfonyl Cyanide or p-Toluenesulfonyl Cyanide to Carbon Radicals Generated from the Acyl Derivatives of N-Hydroxy-2-Thiopyridone Tetrahedron Lett. 1991, 32, 3321-3324 10.1016/S0040-4039(00)92696-0
    • (1991) Tetrahedron Lett. , vol.32 , pp. 3321-3324
    • Barton, D.H.R.1    Jaszberenyi, J.Cs.2    Theodorakis, E.A.3
  • 307
    • 0036456046 scopus 로고    scopus 로고
    • Tin-free Radical Cyanation of Alkyl Iodides and Alkyl Phenyl Tellurides
    • Kim, S.; Song, H.-J. Tin-free Radical Cyanation of Alkyl Iodides and Alkyl Phenyl Tellurides Synlett 2002, 12, 2110-2112 10.1055/s-2002-35589
    • (2002) Synlett , vol.12 , pp. 2110-2112
    • Kim, S.1    Song, H.-J.2
  • 308
    • 33748542324 scopus 로고    scopus 로고
    • Radical-Mediated Alkenylation, Alkynylation, Methanimination, and Cyanation of B-Alkylcatecholboranes
    • Schaffner, A. P.; Darmency, V.; Renaud, P. Radical-Mediated Alkenylation, Alkynylation, Methanimination, and Cyanation of B-Alkylcatecholboranes Angew. Chem., Int. Ed. 2006, 45, 5847-5849 10.1002/anie.200601206
    • (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 5847-5849
    • Schaffner, A.P.1    Darmency, V.2    Renaud, P.3
  • 309
    • 84955092681 scopus 로고
    • Die Addition von Kohlenwasserstoffen an Olefine Eine neue synthetische Methode
    • Giese, B.; Meister, J. Die Addition von Kohlenwasserstoffen an Olefine Eine neue synthetische Methode Chem. Ber. 1977, 110, 2588-2600 10.1002/cber.19771100717
    • (1977) Chem. Ber. , vol.110 , pp. 2588-2600
    • Giese, B.1    Meister, J.2
  • 310
    • 0011430335 scopus 로고
    • Radical Reactions in Organic Synthesis
    • Ramaiah, M. Radical Reactions in Organic Synthesis Tetrahedron 1987, 43, 3541-3676 10.1016/S0040-4020(01)86853-8
    • (1987) Tetrahedron , vol.43 , pp. 3541-3676
    • Ramaiah, M.1
  • 311
    • 25844443429 scopus 로고    scopus 로고
    • Advances in Radical Conjugate Additions
    • Srikanth, G. S. C.; Castle, S. L. Advances in Radical Conjugate Additions Tetrahedron 2005, 61, 10377-10441 10.1016/j.tet.2005.07.077
    • (2005) Tetrahedron , vol.61 , pp. 10377-10441
    • Srikanth, G.S.C.1    Castle, S.L.2
  • 312
    • 84985532045 scopus 로고
    • Steric Effects in the Addition of Alkyl Radicals to Alkenes
    • Giese, B.; Lachhein, S. Steric Effects in the Addition of Alkyl Radicals to Alkenes Angew. Chem., Int. Ed. Engl. 1981, 20, 967 10.1002/anie.198109671
    • (1981) Angew. Chem., Int. Ed. Engl. , vol.20 , pp. 967
    • Giese, B.1    Lachhein, S.2
  • 313
    • 84973444861 scopus 로고    scopus 로고
    • Fe-Catalyzed Hydroalkylation of Olefins with para-Quinone Methides
    • Shen, Y.; Qi, J.; Mao, Z.; Cui, S. Fe-Catalyzed Hydroalkylation of Olefins with para-Quinone Methides Org. Lett. 2016, 18, 2722-2725 10.1021/acs.orglett.6b01173
    • (2016) Org. Lett. , vol.18 , pp. 2722-2725
    • Shen, Y.1    Qi, J.2    Mao, Z.3    Cui, S.4
  • 314
    • 37049103020 scopus 로고
    • Alkyl Groups Migration from Tetra-Alkyl-Silanes, -Germanes, -Stannanes to Carbenium Ions, Effected by Lewuis Acids: A Novel Method for Synthesising Hydrocarbons with a Quaternary Carbon Atom
    • Parnes, Z. N.; Bolestova, G. I.; Akhrem, I. S.; Vol'pin, M. E.; Kursanov, D. N. Alkyl Groups Migration from Tetra-Alkyl-Silanes, -Germanes, -Stannanes to Carbenium Ions, Effected by Lewuis Acids: A Novel Method for Synthesising Hydrocarbons with a Quaternary Carbon Atom J. Chem. Soc., Chem. Commun. 1980, 748-748 10.1039/c39800000748
    • (1980) J. Chem. Soc., Chem. Commun. , pp. 748
    • Parnes, Z.N.1    Bolestova, G.I.2    Akhrem, I.S.3    Vol'Pin, M.E.4    Kursanov, D.N.5
  • 315
    • 0032506645 scopus 로고    scopus 로고
    • Zirconocene-Catalyzed Alkylation of Aryl Alkenes with Alkyl Tosylates, Sulfates and Bromides
    • Terao, J.; Watanabe, T.; Saito, K.; Kambe, N.; Sonoda, N. Zirconocene-Catalyzed Alkylation of Aryl Alkenes with Alkyl Tosylates, Sulfates And Bromides Tetrahedron Lett. 1998, 39, 9201-9204 10.1016/S0040-4039(98)02097-8
    • (1998) Tetrahedron Lett. , vol.39 , pp. 9201-9204
    • Terao, J.1    Watanabe, T.2    Saito, K.3    Kambe, N.4    Sonoda, N.5
  • 316
    • 24944469492 scopus 로고    scopus 로고
    • Control of Selectivity in the Hydromethylation of Olefins via Ligand Modification in Scandocene Catalysts
    • Fontaine, F.-G.; Tilley, T. D. Control of Selectivity in the Hydromethylation of Olefins via Ligand Modification in Scandocene Catalysts Organometallics 2005, 24, 4340-2342 10.1021/om0505460
    • (2005) Organometallics , vol.24 , pp. 2342-4340
    • Fontaine, F.-G.1    Tilley, T.D.2
  • 317
    • 33746416282 scopus 로고
    • Radical Cyclization of Mesitylsulfonylhydrazones
    • Kim, S.; Cho, J. R. Radical Cyclization of Mesitylsulfonylhydrazones Synlett 1992, 1992, 629-630 10.1055/s-1992-21435
    • (1992) Synlett , vol.1992 , pp. 629-630
    • Kim, S.1    Cho, J.R.2
  • 318
    • 37049084804 scopus 로고
    • Azo Anions in Synthesis: α-Amino Carbanion Equivalents from t-Butyldiphenyl-Methylhydrazones
    • Baldwin, J. E.; Adlington, R. M.; Newington, I. M. Azo Anions in Synthesis: α-Amino Carbanion Equivalents from t-Butyldiphenyl-Methylhydrazones J. Chem. Soc., Chem. Commun. 1986, 176-178 10.1039/C39860000176
    • (1986) J. Chem. Soc., Chem. Commun. , pp. 176-178
    • Baldwin, J.E.1    Adlington, R.M.2    Newington, I.M.3
  • 319
    • 0029930055 scopus 로고    scopus 로고
    • An Unexpected Reaction between 2-Aryl-1-Nitro-1-Alkenes and Trialkylgallium Compounds
    • Ying, H.; Yao-Zeng, H.; Cheng-Ming, Z. An Unexpected Reaction Between 2-Aryl-1-Nitro-1-Alkenes and Trialkylgallium Compounds Tetrahedron Lett. 1996, 37, 3347-3350 10.1016/0040-4039(96)00542-4
    • (1996) Tetrahedron Lett. , vol.37 , pp. 3347-3350
    • Ying, H.1    Yao-Zeng, H.2    Cheng-Ming, Z.3
  • 320
    • 0000111727 scopus 로고    scopus 로고
    • Free-Radical Reactions of Trialkylboranes with β-Nitrostyrenes to Generate Alkenes
    • Yao, C.-F.; Chu, C.-M.; Liu, J.-T. Free-Radical Reactions of Trialkylboranes with β-Nitrostyrenes to Generate Alkenes J. Org. Chem. 1998, 63, 719-722 10.1021/jo9716901
    • (1998) J. Org. Chem. , vol.63 , pp. 719-722
    • Yao, C.-F.1    Chu, C.-M.2    Liu, J.-T.3
  • 321
    • 0035926282 scopus 로고    scopus 로고
    • Novel Synthesis of Alkenes via Triethylaluminum-Induced Free Radical Reactions of Alkyl Iodides and β-nitrostyrenes
    • Liu, J.-Y.; Liu, J.-T.; Yao, C.-F. Novel Synthesis of Alkenes via Triethylaluminum-Induced Free Radical Reactions of Alkyl Iodides and β-nitrostyrenes Tetrahedron Lett. 2001, 42, 3613-3615 10.1016/S0040-4039(01)00519-6
    • (2001) Tetrahedron Lett. , vol.42 , pp. 3613-3615
    • Liu, J.-Y.1    Liu, J.-T.2    Yao, C.-F.3
  • 322
    • 4143128102 scopus 로고    scopus 로고
    • A Highly Diastereoselective Tandem Radical Reaction. Facile Three-Component Routes to Protected (E)-Polysubstituted Homoallylic Alcohols
    • Jang, Y.-J.; Wu, J.; Lin, Y.-F.; Yao, C.-F. A Highly Diastereoselective Tandem Radical Reaction. Facile Three-Component Routes to Protected (E)-Polysubstituted Homoallylic Alcohols Tetrahedron 2004, 60, 6565-6574 10.1016/j.tet.2004.06.001
    • (2004) Tetrahedron , vol.60 , pp. 6565-6574
    • Jang, Y.-J.1    Wu, J.2    Lin, Y.-F.3    Yao, C.-F.4
  • 323
    • 0001574188 scopus 로고
    • Alkylation of β-Substituted Styrenes by a Free Radical Addition-Elimination Sequence
    • Russell, G. A.; Tashtoush, H.; Ngoviwatchai, P. Alkylation of β-Substituted Styrenes by a Free Radical Addition-Elimination Sequence J. Am. Chem. Soc. 1984, 106, 4622-4623 10.1021/ja00328a057
    • (1984) J. Am. Chem. Soc. , vol.106 , pp. 4622-4623
    • Russell, G.A.1    Tashtoush, H.2    Ngoviwatchai, P.3
  • 324
    • 84942198086 scopus 로고    scopus 로고
    • Synthesis of Oxindoles via Iron-Mediated Hydrometallation-Cyclization of N-Arylacrylamides
    • Gui, Q.; Hu, L.; Chen, X.; Liu, J.; Tan, Z. Synthesis of Oxindoles via Iron-Mediated Hydrometallation-Cyclization of N-Arylacrylamides Asian J. Org. Chem. 2015, 4, 870-874 10.1002/ajoc.201500217
    • (2015) Asian J. Org. Chem. , vol.4 , pp. 870-874
    • Gui, Q.1    Hu, L.2    Chen, X.3    Liu, J.4    Tan, Z.5
  • 325
    • 84973513388 scopus 로고    scopus 로고
    • Synthesis of the Privileged 8-Arylmenthol Class by Radical Arylation of Isopulegol
    • Crossley, S. W. M.; Martinez, R. M.; Guevara-Zuluaga, S.; Shenvi, R. A. Synthesis of the Privileged 8-Arylmenthol Class by Radical Arylation of Isopulegol Org. Lett. 2016, 18, 2620-2623 10.1021/acs.orglett.6b01047
    • (2016) Org. Lett. , vol.18 , pp. 2620-2623
    • Crossley, S.W.M.1    Martinez, R.M.2    Guevara-Zuluaga, S.3    Shenvi, R.A.4
  • 326
    • 0001899091 scopus 로고
    • Cobalt(II) Catalyzed Coupling Reaction of a,b-Unsaturated Compounds with Aldehydes by the Use of Phenylsilane. New Method for Preparation of b-Hydroxy Nitriles, Amides, and Esters
    • Isayama, S.; Mukaiyama, T. Cobalt(II) Catalyzed Coupling Reaction of a,b-Unsaturated Compounds with Aldehydes by the Use of Phenylsilane. New Method for Preparation of b-Hydroxy Nitriles, Amides, and Esters Chem. Lett. 1989, 18, 2005-2008 10.1246/cl.1989.2005
    • (1989) Chem. Lett. , vol.18 , pp. 2005-2008
    • Isayama, S.1    Mukaiyama, T.2
  • 327
    • 0033935920 scopus 로고    scopus 로고
    • Aymmetric Catalysis of Aldol Reactions with Chiral Lewis Bases
    • Denmark, S. E.; Stavenger, R. A. Aymmetric Catalysis of Aldol Reactions with Chiral Lewis Bases Acc. Chem. Res. 2000, 33, 432-440 10.1021/ar960027g
    • (2000) Acc. Chem. Res. , vol.33 , pp. 432-440
    • Denmark, S.E.1    Stavenger, R.A.2
  • 328
    • 0037243649 scopus 로고    scopus 로고
    • Enones as Latent Enolates in Catalytic Processes: Catalytic Cycloreductions, Cycloaddition and Cycloisomerization
    • Huddleston, R. R.; Krische, M. J. Enones as Latent Enolates in Catalytic Processes: Catalytic Cycloreductions, Cycloaddition and Cycloisomerization Synlett 2003, 0012-0021 10.1055/s-2003-36213
    • (2003) Synlett , pp. 0012-0021
    • Huddleston, R.R.1    Krische, M.J.2
  • 330
    • 33845183776 scopus 로고
    • The Palladium-Catalyzed Directed Aldol Reaction of Aldehydes with Ketone Enolates Generated by the Decarboxylation of Allyl b-Keto Carboxylates under Neutral Conditions
    • Nokami, J.; Mandai, T.; Watanabe, H.; Ohyama, H.; Tsuji, J. The Palladium-Catalyzed Directed Aldol Reaction of Aldehydes with Ketone Enolates Generated by the Decarboxylation of Allyl b-Keto Carboxylates under Neutral Conditions J. Am. Chem. Soc. 1989, 111, 4126-4127 10.1021/ja00193a069
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 4126-4127
    • Nokami, J.1    Mandai, T.2    Watanabe, H.3    Ohyama, H.4    Tsuji, J.5
  • 331
    • 0032537679 scopus 로고    scopus 로고
    • A Mild Aldol Reaction of Aryl Aldehydes through Palladium-Catalyzed Hydrosilation of a,b-Unsaturated Carbonyl Compounds with Trichlorosilane
    • Kiyooka, S.; Shimizu, A.; Torii, S. A Mild Aldol Reaction of Aryl Aldehydes through Palladium-Catalyzed Hydrosilation of a,b-Unsaturated Carbonyl Compounds with Trichlorosilane Tetrahedron Lett. 1998, 39, 5237-5238 10.1016/S0040-4039(98)01030-2
    • (1998) Tetrahedron Lett. , vol.39 , pp. 5237-5238
    • Kiyooka, S.1    Shimizu, A.2    Torii, S.3
  • 332
    • 0001494417 scopus 로고    scopus 로고
    • Enantio- and Diastereoselective Reductive Aldol Reactions with Iridium Pybox Catalysts
    • Zhao, C.-X.; Duffey, M. O.; Taylor, S. J.; Morken, J. P. Enantio- and Diastereoselective Reductive Aldol Reactions with Iridium Pybox Catalysts Org. Lett. 2001, 3, 1829-1831 10.1021/ol015859f
    • (2001) Org. Lett. , vol.3 , pp. 1829-1831
    • Zhao, C.-X.1    Duffey, M.O.2    Taylor, S.J.3    Morken, J.P.4
  • 334
    • 0000556498 scopus 로고
    • Synthesis of h1-Oxygen-Bound Rhodium Enolates. Applications to Catalytic Aldol Chemistry
    • Slough, G. A.; Bergman, R. G.; Heathcock, H. Synthesis of h1-Oxygen-Bound Rhodium Enolates. Applications to Catalytic Aldol Chemistry J. Am. Chem. Soc. 1989, 111, 938-949 10.1021/ja00185a025
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 938-949
    • Slough, G.A.1    Bergman, R.G.2    Heathcock, H.3
  • 335
    • 0034630894 scopus 로고    scopus 로고
    • Rhodium-Catalyzed Enantioselective Reductive Aldol Reaction
    • Taylor, S. J.; Duffey, M. O.; Morken, J. P. Rhodium-Catalyzed Enantioselective Reductive Aldol Reaction J. Am. Chem. Soc. 2000, 122, 4528-4529 10.1021/ja9944453
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 4528-4529
    • Taylor, S.J.1    Duffey, M.O.2    Morken, J.P.3
  • 336
    • 84897481492 scopus 로고    scopus 로고
    • Cobalt-Catalyzed Reductive Carboxylation of a,b-Unsaturated Nitriles with Carbon Dioxide
    • Hayashi, C.; Hayashi, T.; Kikuchi, S.; Yamada, T. Cobalt-Catalyzed Reductive Carboxylation of a,b-Unsaturated Nitriles with Carbon Dioxide Chem. Lett. 2014, 43, 565-567 10.1246/cl.131163
    • (2014) Chem. Lett. , vol.43 , pp. 565-567
    • Hayashi, C.1    Hayashi, T.2    Kikuchi, S.3    Yamada, T.4
  • 337
    • 0034803441 scopus 로고    scopus 로고
    • Diastereoselective Cobalt-Catalyzed Aldol and Michael Cycloreductions
    • Baik, T.-G.; Luis, A. L.; Wang, L.-C.; Krische, M. J. Diastereoselective Cobalt-Catalyzed Aldol and Michael Cycloreductions J. Am. Chem. Soc. 2001, 123, 5112-5113 10.1021/ja0040971
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 5112-5113
    • Baik, T.-G.1    Luis, A.L.2    Wang, L.-C.3    Krische, M.J.4
  • 338
    • 0034809351 scopus 로고    scopus 로고
    • Diastereoselective Metal-Catalyzed [2 + 2] Cycloaddition of Bis-enones
    • Baik, T.-G.; Luis, A. L.; Wang, L.-C.; Krische, M. J. Diastereoselective Metal-Catalyzed [2 + 2] Cycloaddition of Bis-enones J. Am. Chem. Soc. 2001, 123, 6716-6717 10.1021/ja010800p
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 6716-6717
    • Baik, T.-G.1    Luis, A.L.2    Wang, L.-C.3    Krische, M.J.4
  • 339
    • 35748973304 scopus 로고    scopus 로고
    • Tin-Free Radical Carbon-Carbon Bond-Forming Reactions Based on α-Scission of Alkylsulfonyl Radicals
    • Kim, S.; Kim, S. Tin-Free Radical Carbon-Carbon Bond-Forming Reactions Based on α-Scission of Alkylsulfonyl Radicals Bull. Chem. Soc. Jpn. 2007, 80, 809-822 10.1246/bcsj.80.809
    • (2007) Bull. Chem. Soc. Jpn. , vol.80 , pp. 809-822
    • Kim, S.1    Kim, S.2
  • 340
    • 53549085446 scopus 로고    scopus 로고
    • Catalytic Hydrochlorination of Unactivated Olefins with Para-Toluenesulfonyl Chloride
    • Gaspar, B.; Carreira, E. M. Catalytic Hydrochlorination of Unactivated Olefins with Para-Toluenesulfonyl Chloride Angew. Chem., Int. Ed. 2008, 47, 5758-5760 10.1002/anie.200801760
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 5758-5760
    • Gaspar, B.1    Carreira, E.M.2
  • 342
    • 84950237704 scopus 로고    scopus 로고
    • A Concise Approach to Paxilline Indole Diterpenes
    • George, D. T.; Kuenstner, E. J.; Pronin, S. V. A Concise Approach to Paxilline Indole Diterpenes J. Am. Chem. Soc. 2015, 137, 15410-15413 10.1021/jacs.5b11129
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 15410-15413
    • George, D.T.1    Kuenstner, E.J.2    Pronin, S.V.3
  • 344
    • 84985123200 scopus 로고
    • Synthetic Methods and Reactions II. Hydrofluorination of Alkenes, Cyclopropane and Alkynes with Poly-Hydrogen Fluoride/Pyridine (Trialkamine) Reagents
    • Olah, G. A.; Nojima, M.; Kerekes, I. Synthetic Methods and Reactions II. Hydrofluorination of Alkenes, Cyclopropane and Alkynes with Poly-Hydrogen Fluoride/Pyridine (Trialkamine) Reagents Synthesis 1973, 1973, 779-780 10.1055/s-1973-22297
    • (1973) Synthesis , vol.1973 , pp. 779-780
    • Olah, G.A.1    Nojima, M.2    Kerekes, I.3
  • 347
    • 84863483648 scopus 로고    scopus 로고
    • Silver-Catalyzed Decarboxylative Fluorination of Aliphatic Carboxylic Acids in Aqueous Solution
    • Yin, F.; Wang, Z.; Li, Z.; Li, C. Silver-Catalyzed Decarboxylative Fluorination of Aliphatic Carboxylic Acids in Aqueous Solution J. Am. Chem. Soc. 2012, 134, 10401-10404 10.1021/ja3048255
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 10401-10404
    • Yin, F.1    Wang, Z.2    Li, Z.3    Li, C.4
  • 348
    • 64349105617 scopus 로고    scopus 로고
    • Electrophilic Fluorination with N-F Reagents
    • John Wiley & Sons, Inc. Vol
    • Baudoux, J.; Cahard, D. Electrophilic Fluorination with N-F Reagents. In Organic Reactions; John Wiley & Sons, Inc.: 2004; Vol. 69, pp 347-672.
    • (2004) Organic Reactions , vol.69 , pp. 347-672
    • Baudoux, J.1    Cahard, D.2
  • 349
    • 84865431754 scopus 로고    scopus 로고
    • 4-Mediated Free Radical Hydrofluorination of Unactivated Alkenes
    • 4-Mediated Free Radical Hydrofluorination of Unactivated Alkenes J. Am. Chem. Soc. 2012, 134, 13588-13591 10.1021/ja3063716
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 13588-13591
    • Barker, T.J.1    Boger, D.L.2
  • 350
    • 0032823766 scopus 로고    scopus 로고
    • Efficient Synthesis of 4-Fluorocyclohexa-2,5-dienone Derivatives Using N-Fluoro-1,4-diazoniabicyclo[2.2.2]octane Salt Analogues
    • Stavber, S.; Jereb, M.; Zupan, M. Efficient Synthesis of 4-Fluorocyclohexa-2,5-dienone Derivatives Using N-Fluoro-1,4-diazoniabicyclo[2.2.2]octane Salt Analogues Synlett 1999, 1999, 1375-1378 10.1055/s-1999-2840
    • (1999) Synlett , vol.1999 , pp. 1375-1378
    • Stavber, S.1    Jereb, M.2    Zupan, M.3
  • 351
    • 84862538749 scopus 로고    scopus 로고
    • Iron(III)-Catalyzed Conia-Ene Cyclization of 2-Alkynic 1,3-Dicarbonyl Compounds
    • Chan, L. Y.; Kim, S.; Park, Y.; Lee, P. H. Iron(III)-Catalyzed Conia-Ene Cyclization of 2-Alkynic 1,3-Dicarbonyl Compounds J. Org. Chem. 2012, 77, 5239-5244 10.1021/jo300957q
    • (2012) J. Org. Chem. , vol.77 , pp. 5239-5244
    • Chan, L.Y.1    Kim, S.2    Park, Y.3    Lee, P.H.4
  • 352
    • 84859613811 scopus 로고    scopus 로고
    • Facile Synthesis of Azaspirocycles via Iron Trichloride-Promoted Cyclization/Chlorination of Cyclic 8-Aryl-5-aza-5-tosyl-2-en-7-yn-1-ols
    • Yeh, M.-C. P.; Fang, C.-W.; Lin, H.-H. Facile Synthesis of Azaspirocycles via Iron Trichloride-Promoted Cyclization/Chlorination of Cyclic 8-Aryl-5-aza-5-tosyl-2-en-7-yn-1-ols Org. Lett. 2012, 14, 1830-1833 10.1021/ol300434m
    • (2012) Org. Lett. , vol.14 , pp. 1830-1833
    • Yeh, M.-C.P.1    Fang, C.-W.2    Lin, H.-H.3
  • 354
    • 84944038672 scopus 로고    scopus 로고
    • Non-Classical Selectivities in the Reduction of Alkenes by Cobalt-Mediated Hydrogen Atom Transfer
    • Ma, X. S.; Herzon, S. B. Non-Classical Selectivities in the Reduction of Alkenes by Cobalt-Mediated Hydrogen Atom Transfer Chem. Sci. 2015, 6, 6250-6255 10.1039/C5SC02476E
    • (2015) Chem. Sci. , vol.6 , pp. 6250-6255
    • Ma, X.S.1    Herzon, S.B.2
  • 355
    • 84869061478 scopus 로고    scopus 로고
    • Ananikov, V. P. Tanaka, M. Topics in Organometallics Chemistry 43; Springer: Berlin
    • Ogawa, A. In Hydrofunctionalization; Ananikov, V. P.; Tanaka, M., Eds.; Topics in Organometallics Chemistry 43; Springer: Berlin, 2012; pp 325-360.
    • (2012) Hydrofunctionalization , pp. 325-360
    • Ogawa, A.1
  • 356
    • 84887097589 scopus 로고    scopus 로고
    • Highly Regioselective Palladium-Catalyzed Double Hydroselenation of Terminal Alkynes with Benzeselenol in the Presence of Acetic Acid
    • Ikeda, T.; Tamai, T.; Daitou, M.; Minamida, Y.; Mitamura, T. et al. Highly Regioselective Palladium-Catalyzed Double Hydroselenation of Terminal Alkynes with Benzeselenol in the Presence of Acetic Acid Chem. Lett. 2013, 42, 1383-1385 10.1246/cl.130641
    • (2013) Chem. Lett. , vol.42 , pp. 1383-1385
    • Ikeda, T.1    Tamai, T.2    Daitou, M.3    Minamida, Y.4    Mitamura, T.5
  • 357
    • 0004562427 scopus 로고
    • Hemin-Catalyzed Addition Reactions of Thiophenols to Styrene
    • Kano, K.; Takeuchi, M.; Hashimoto, S.; Yoshidat, Z. Hemin-Catalyzed Addition Reactions of Thiophenols to Styrene Chem. Lett. 1990, 19, 1381-1384 10.1246/cl.1990.1381
    • (1990) Chem. Lett. , vol.19 , pp. 1381-1384
    • Kano, K.1    Takeuchi, M.2    Hashimoto, S.3    Yoshidat, Z.4
  • 358
    • 0000215648 scopus 로고
    • (Porphinato)iron-Catalyzed Addition Reactions of Thiols to Alkenes via (s-Alkyl)iron(II) Complexes
    • Takeuchi, M.; Shimakoshi, H.; Kano, K. (Porphinato)iron-Catalyzed Addition Reactions of Thiols to Alkenes via (s-Alkyl)iron(II) Complexes Organometallics 1994, 13, 1208-1213 10.1021/om00016a025
    • (1994) Organometallics , vol.13 , pp. 1208-1213
    • Takeuchi, M.1    Shimakoshi, H.2    Kano, K.3
  • 359
    • 79961093490 scopus 로고    scopus 로고
    • Regioselective Cobalt-Catalyzed Addition of Sulfides to Unactivated Alkenes
    • Girijavallabhan, V.; Alvarez, C.; Njoroge, F. G. Regioselective Cobalt-Catalyzed Addition of Sulfides to Unactivated Alkenes J. Org. Chem. 2011, 76, 6442-6446 10.1021/jo201016z
    • (2011) J. Org. Chem. , vol.76 , pp. 6442-6446
    • Girijavallabhan, V.1    Alvarez, C.2    Njoroge, F.G.3
  • 360
    • 0000155174 scopus 로고
    • Mechanism of the Cobalt Carbonyl-Catalyzed Homogeneous Hydrogenation of Aromatic Hydrocarbons
    • Feder, H. M.; Halpern, J. Mechanism of the Cobalt Carbonyl-Catalyzed Homogeneous Hydrogenation of Aromatic Hydrocarbons J. Am. Chem. Soc. 1975, 97, 7186-7188 10.1021/ja00857a051
    • (1975) J. Am. Chem. Soc. , vol.97 , pp. 7186-7188
    • Feder, H.M.1    Halpern, J.2
  • 361
    • 0000898468 scopus 로고
    • Hydrogenation of α-Methylstyrene by Hydridopentacarbonylmanganese (I). Evidence for a Free-Radical Mechanism
    • Sweany, R. L.; Halpern, J. Hydrogenation of α-Methylstyrene by Hydridopentacarbonylmanganese (I). Evidence for a Free-Radical Mechanism J. Am. Chem. Soc. 1977, 99, 8335-8337 10.1021/ja00467a045
    • (1977) J. Am. Chem. Soc. , vol.99 , pp. 8335-8337
    • Sweany, R.L.1    Halpern, J.2
  • 362
    • 33748226168 scopus 로고
    • Otto Roelen, Pioneer in Industrial Homogeneous Catalysis
    • Cornils, B.; Herrmann, W. A.; Rasch, M. Otto Roelen, Pioneer in Industrial Homogeneous Catalysis Angew. Chem., Int. Ed. Engl. 1994, 33, 2144-2163 10.1002/anie.199421441
    • (1994) Angew. Chem., Int. Ed. Engl. , vol.33 , pp. 2144-2163
    • Cornils, B.1    Herrmann, W.A.2    Rasch, M.3
  • 363
    • 0344798306 scopus 로고
    • Hydroformylation of Unsaturated Compounds with a Cobalt Carbonyl Catalyst
    • Adkins, H.; Krsek, G. Hydroformylation of Unsaturated Compounds with a Cobalt Carbonyl Catalyst J. Am. Chem. Soc. 1949, 71, 3051-3055 10.1021/ja01177a032
    • (1949) J. Am. Chem. Soc. , vol.71 , pp. 3051-3055
    • Adkins, H.1    Krsek, G.2
  • 366
    • 0001629246 scopus 로고
    • Selective Hydrogenation of Polynuclear Aromatic Hydrocarbons
    • Friedman, S.; Metlin, S.; Svedi, A.; Wender, I. Selective Hydrogenation of Polynuclear Aromatic Hydrocarbons J. Org. Chem. 1959, 24, 1287-1289 10.1021/jo01091a033
    • (1959) J. Org. Chem. , vol.24 , pp. 1287-1289
    • Friedman, S.1    Metlin, S.2    Svedi, A.3    Wender, I.4
  • 367
    • 84945786529 scopus 로고
    • Reactions Catalyzed by Pentacyanocobaltate(II)
    • Kwiatek, J. Reactions Catalyzed by Pentacyanocobaltate(II) Catal. Rev.: Sci. Eng. 1968, 1, 37-72 10.1080/01614946808064700
    • (1968) Catal. Rev.: Sci. Eng. , vol.1 , pp. 37-72
    • Kwiatek, J.1
  • 368
    • 84990106036 scopus 로고
    • Studies on the Catalytic Oxido-reduction by Some Metallic Complex Salts. XVII
    • Iguchi, M. Studies on the Catalytic Oxido-reduction by Some Metallic Complex Salts. XVII Nippon Kagaku Kaishi 1942, 63, 634-643 10.1246/nikkashi1921.63.634
    • (1942) Nippon Kagaku Kaishi , vol.63 , pp. 634-643
    • Iguchi, M.1
  • 369
    • 85021465954 scopus 로고
    • Catalytic Hydrogenation of Organic Compounds by Pentacyanocobaltate(II)
    • Kwiatek, J.; Mador, I. L.; Seyler, J. K. Catalytic Hydrogenation of Organic Compounds by Pentacyanocobaltate(II) J. Am. Chem. Soc. 1962, 84, 304-305 10.1021/ja00861a034
    • (1962) J. Am. Chem. Soc. , vol.84 , pp. 304-305
    • Kwiatek, J.1    Mador, I.L.2    Seyler, J.K.3
  • 370
    • 84891530257 scopus 로고
    • Catalytic Hydrogenation by Pentacyanopentacobaltate (II)
    • Kwiatek, J.; Mador, I. L.; Seyler, J. K. Catalytic Hydrogenation by Pentacyanopentacobaltate (II) Adv. Chem. Ser. 1962, 37, 201-215 10.1021/ba-1963-0037.ch015
    • (1962) Adv. Chem. Ser. , vol.37 , pp. 201-215
    • Kwiatek, J.1    Mador, I.L.2    Seyler, J.K.3
  • 371
    • 33646438595 scopus 로고
    • Homogeneous Catalysis by Coordination Compounds
    • Halpern, J. Homogeneous Catalysis by Coordination Compounds Adv. Chem. Ser. 1974, 70, 1-24 10.1021/ba-1968-0070.ch001
    • (1974) Adv. Chem. Ser. , vol.70 , pp. 1-24
    • Halpern, J.1
  • 372
    • 0013336416 scopus 로고
    • Kinetics of the Addition of Hydridopentacyanocobaltate(III) to some α,β-Unsaturated Compounds
    • Halpern, J.; Wong, L.-Y. Kinetics of the Addition of Hydridopentacyanocobaltate(III) to some α,β-Unsaturated Compounds J. Am. Chem. Soc. 1968, 90, 6665-6669 10.1021/ja01026a018
    • (1968) J. Am. Chem. Soc. , vol.90 , pp. 6665-6669
    • Halpern, J.1    Wong, L.-Y.2
  • 374
    • 0022047222 scopus 로고
    • Free Radical Mechanisms in Organometallic and Bioorganometallic Chemistry
    • Halpern, J. Free Radical Mechanisms in Organometallic and Bioorganometallic Chemistry Pure Appl. Chem. 1986, 58, 575-584 10.1351/pac198658040575
    • (1986) Pure Appl. Chem. , vol.58 , pp. 575-584
    • Halpern, J.1
  • 375
    • 85005746639 scopus 로고
    • Hydrogen-Atom Transfer Reactions of Transition-Metal Hydrides
    • Eisenberg, D. C.; Norton, J. R. Hydrogen-Atom Transfer Reactions of Transition-Metal Hydrides Isr. J. Chem. 1991, 31, 55-66 10.1002/ijch.199100006
    • (1991) Isr. J. Chem. , vol.31 , pp. 55-66
    • Eisenberg, D.C.1    Norton, J.R.2
  • 377
    • 84976243112 scopus 로고    scopus 로고
    • Conjuring a Supernatural Product - DelMarine
    • Wan, K. K.; Shenvi, R. A. Conjuring a Supernatural Product-DelMarine Synlett 2016, 27, 1145-1164 10.1055/s-0035-1561329
    • (2016) Synlett , vol.27 , pp. 1145-1164
    • Wan, K.K.1    Shenvi, R.A.2
  • 378
    • 84981737520 scopus 로고
    • Stereochemistry of Reduction of Methylenecyclohexanes by Dissolving Metals
    • Ficini, J.; Francilette, J.; Touzin, A. M. Stereochemistry of Reduction of Methylenecyclohexanes by Dissolving Metals J. Chem. Res., Synop. 1979, 150-151
    • (1979) J. Chem. Res., Synop. , pp. 150-151
    • Ficini, J.1    Francilette, J.2    Touzin, A.M.3
  • 379
    • 0000255655 scopus 로고
    • Diastereofacial Selectivity in Reactions of Substituted Cyclohexyl Radicals. An Experimental and Theoretical Study
    • Damm, W.; Giese, B.; Hartung, J.; Hasskerl, T.; Houk, K. N.; Hueter, O.; Zipse, H. Diastereofacial Selectivity in Reactions of Substituted Cyclohexyl Radicals. An Experimental and Theoretical Study J. Am. Chem. Soc. 1992, 114, 4067-4079 10.1021/ja00037a007
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 4067-4079
    • Damm, W.1    Giese, B.2    Hartung, J.3    Hasskerl, T.4    Houk, K.N.5    Hueter, O.6    Zipse, H.7
  • 380
    • 4143095276 scopus 로고
    • Alternative and Stereoselective Synthesis of 8β(H)-Drimane, A Bicyclic Sesquiterpane of Widespread Occurrence in Petroleum
    • González-Sierra, M.; Laborde, M. A.; Rúveda, E. A. Alternative and Stereoselective Synthesis of 8β(H)-Drimane, A Bicyclic Sesquiterpane of Widespread Occurrence in Petroleum Synth. Commun. 1987, 17, 431-441 10.1080/00397918708063921
    • (1987) Synth. Commun. , vol.17 , pp. 431-441
    • González-Sierra, M.1    Laborde, M.A.2    Rúveda, E.A.3
  • 381
    • 84875353573 scopus 로고    scopus 로고
    • Herzon Total Syntheses of (-)-Acutumine and (-)-Dechloroacutumine
    • King, S. M.; Calandra, N. A.; Herzon, S. B. Herzon Total Syntheses of (-)-Acutumine and (-)-Dechloroacutumine Angew. Chem., Int. Ed. 2013, 52, 3642-3645 10.1002/anie.201210076
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 3642-3645
    • King, S.M.1    Calandra, N.A.2    Herzon, S.B.3
  • 382
    • 0000259344 scopus 로고
    • Selective Reduction of Mono- and Disubstituted Olefins by Sodium Borohydride and Cobalt(II)
    • Chung, S.-K. Selective Reduction of Mono- and Disubstituted Olefins by Sodium Borohydride and Cobalt(II) J. Org. Chem. 1979, 44, 1014-1016 10.1021/jo01320a033
    • (1979) J. Org. Chem. , vol.44 , pp. 1014-1016
    • Chung, S.-K.1
  • 383
    • 0012918150 scopus 로고    scopus 로고
    • Methods of Enhancement of Reactivity and Selectivity of Sodium Borohydride for Applications in Organic Synthesis
    • Periasamy, M.; Thirumalaikumar, M. Methods of Enhancement of Reactivity and Selectivity of Sodium Borohydride for Applications in Organic Synthesis J. Organomet. Chem. 2000, 609, 137-151 10.1016/S0022-328X(00)00210-2
    • (2000) J. Organomet. Chem. , vol.609 , pp. 137-151
    • Periasamy, M.1    Thirumalaikumar, M.2
  • 384
    • 0002931218 scopus 로고
    • Studies on the Mechanism of Transition-Metal-Assisted Sodium Borohydride and Lithium Aluminum Hydride Reductions
    • Osby, J. O.; Heinzman, S. W.; Ganem, B. Studies on the Mechanism of Transition-Metal-Assisted Sodium Borohydride and Lithium Aluminum Hydride Reductions J. Am. Chem. Soc. 1986, 108, 67-72 10.1021/ja00261a011
    • (1986) J. Am. Chem. Soc. , vol.108 , pp. 67-72
    • Osby, J.O.1    Heinzman, S.W.2    Ganem, B.3
  • 386
    • 0028133038 scopus 로고
    • Total Synthesis of (±)-Epicubenol
    • Cane, D. E.; Tandon, M. Total Synthesis of (±)-Epicubenol Tetrahedron Lett. 1994, 35, 5351-5354 10.1016/S0040-4039(00)73497-6
    • (1994) Tetrahedron Lett. , vol.35 , pp. 5351-5354
    • Cane, D.E.1    Tandon, M.2
  • 387
    • 0028967594 scopus 로고
    • Construction of Oxocane Skeleton via Unusually Regioselective C-C Bond Forming Cyclization: Synthesis of (+) and (-)-Lauthisan
    • Suh, Y.-G.; Koo, B.-A.; Kim, E.-N.; Choi, N.-S. Construction of Oxocane Skeleton via Unusually Regioselective C-C Bond Forming Cyclization: Synthesis of (+) and (-)-Lauthisan Tetrahedron Lett. 1995, 36, 2089-2092 10.1016/0040-4039(95)00217-Z
    • (1995) Tetrahedron Lett. , vol.36 , pp. 2089-2092
    • Suh, Y.-G.1    Koo, B.-A.2    Kim, E.-N.3    Choi, N.-S.4
  • 388
    • 0032500142 scopus 로고    scopus 로고
    • Synthesis of the C19 through C27 Segment of Okadaic Acid Using Vinylogous Urethane Aldol Chemistry: Part III
    • Dankwardt, J. W.; Dankwardt, S. M.; Schlessinger, R. H. Synthesis of the C19 through C27 Segment of Okadaic Acid Using Vinylogous Urethane Aldol Chemistry: Part III Tetrahedron Lett. 1998, 39, 4979 10.1016/S0040-4039(98)00973-3
    • (1998) Tetrahedron Lett. , vol.39 , pp. 4979
    • Dankwardt, J.W.1    Dankwardt, S.M.2    Schlessinger, R.H.3
  • 389
    • 18644377487 scopus 로고    scopus 로고
    • Structure-Based Design: Synthesis and Biological Evaluation of a Series of Novel Cycloamide-Derived HIV-1 Protease Inhibitors
    • Ghosh, A. K.; Swanson, L. M.; Cho, H.; Leshchenko, S.; Hussain, K. A.; Kay, S.; Walters, D. E.; Koh, Y.; Mitsuya, H. Structure-Based Design: Synthesis and Biological Evaluation of a Series of Novel Cycloamide-Derived HIV-1 Protease Inhibitors J. Med. Chem. 2005, 48, 3576-3585 10.1021/jm050019i
    • (2005) J. Med. Chem. , vol.48 , pp. 3576-3585
    • Ghosh, A.K.1    Swanson, L.M.2    Cho, H.3    Leshchenko, S.4    Hussain, K.A.5    Kay, S.6    Walters, D.E.7    Koh, Y.8    Mitsuya, H.9
  • 390
    • 80053601493 scopus 로고    scopus 로고
    • [2,3]-Wittig Rearrangement Approach to Iminosugar C-glycosides: 5-epi-Ethylfagomine, 2-epi-5-Deoxyadenophorine and Formal Synthesis of Indolizidine 167B and 209D
    • Chandrasekhar, B.; Prasada Rao, J.; Venkateswara Rao, B.; Naresh, P. [2,3]-Wittig Rearrangement Approach to Iminosugar C-glycosides: 5-epi-Ethylfagomine, 2-epi-5-Deoxyadenophorine and Formal Synthesis of Indolizidine 167B and 209D Tetrahedron Lett. 2011, 52, 5921-5925 10.1016/j.tetlet.2011.08.084
    • (2011) Tetrahedron Lett. , vol.52 , pp. 5921-5925
    • Chandrasekhar, B.1    Prasada Rao, J.2    Venkateswara Rao, B.3    Naresh, P.4
  • 391
    • 84926142255 scopus 로고    scopus 로고
    • Total Synthesis of the Leucosceptroid Family of Natural Products
    • Hugelshofer, C. L.; Magauer, T. Total Synthesis of the Leucosceptroid Family of Natural Products J. Am. Chem. Soc. 2015, 137, 3807-3810 10.1021/jacs.5b02021
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 3807-3810
    • Hugelshofer, C.L.1    Magauer, T.2
  • 392
    • 0542441253 scopus 로고
    • Porphyrinatoiron-Catalysed Reduction of Styrene with Sodium Borohydride: Proposed [s]-Alkyliron(III) Complex as an Intermediate
    • Kano, K.; Takeuchi, M.; Hashimoto, S.; Yoshida, Z.-i. Porphyrinatoiron-Catalysed Reduction of Styrene with Sodium Borohydride: Proposed [s]-Alkyliron(III) Complex as an Intermediate J. Chem. Soc., Chem. Commun. 1991, 1728-1729 10.1039/C39910001728
    • (1991) J. Chem. Soc., Chem. Commun. , pp. 1728-1729
    • Kano, K.1    Takeuchi, M.2    Hashimoto, S.3    Yoshida, Z.-I.4
  • 394
    • 84941798259 scopus 로고    scopus 로고
    • Mechanistic Understanding of Transition-Metal Catalyzed Olefin Isomerization: Transition-Metal-Catalyzed Olefin Isomerization: Metal-Hydride Insertion-Elimination vs. -Allyl Pathways
    • Biswas, S. Mechanistic Understanding of Transition-Metal Catalyzed Olefin Isomerization: Transition-Metal-Catalyzed Olefin Isomerization: Metal-Hydride Insertion-Elimination vs. -Allyl Pathways Comments Inorg. Chem. 2015, 35, 300-330 10.1080/02603594.2015.1059325
    • (2015) Comments Inorg. Chem. , vol.35 , pp. 300-330
    • Biswas, S.1
  • 396
    • 84927945526 scopus 로고    scopus 로고
    • The Cobalt Hydride that Never Was: Revisiting Schrauzer's Hydridocobaloxime'
    • Lacy, D. C.; Roberts, G. M.; Peters, J. C. The Cobalt Hydride that Never Was: Revisiting Schrauzer's Hydridocobaloxime' J. Am. Chem. Soc. 2015, 137, 4860-4864 10.1021/jacs.5b01838
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 4860-4864
    • Lacy, D.C.1    Roberts, G.M.2    Peters, J.C.3
  • 398
    • 84907849424 scopus 로고    scopus 로고
    • Dihydrogen Activation by Cobaloximes with Various Axial Ligands
    • Li, G.; Estes, D. P.; Norton, J. R.; Ruccolo, S.; Sattler, A.; Sattler, W. Dihydrogen Activation by Cobaloximes with Various Axial Ligands Inorg. Chem. 2014, 53, 10743-10747 10.1021/ic501975r
    • (2014) Inorg. Chem. , vol.53 , pp. 10743-10747
    • Li, G.1    Estes, D.P.2    Norton, J.R.3    Ruccolo, S.4    Sattler, A.5    Sattler, W.6
  • 399
  • 400
    • 84891337963 scopus 로고    scopus 로고
    • Bis(imino)pyridine Cobalt-Catalyzed Alkene Isomerization-Hydroboration: A Strategy for Remote Hydrofunctionalization with Terminal Selectivity
    • Obligacion, J. V.; Chirik, P. J. Bis(imino)pyridine Cobalt-Catalyzed Alkene Isomerization-Hydroboration: A Strategy for Remote Hydrofunctionalization with Terminal Selectivity J. Am. Chem. Soc. 2013, 135, 19107-19110 10.1021/ja4108148
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 19107-19110
    • Obligacion, J.V.1    Chirik, P.J.2
  • 401
    • 84863465368 scopus 로고    scopus 로고
    • Stereoselective Alkene Isomerization over One Position
    • Larsen, C. R.; Grotjahn, D. B. Stereoselective Alkene Isomerization over One Position J. Am. Chem. Soc. 2012, 134, 10357-10360 10.1021/ja3036477
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 10357-10360
    • Larsen, C.R.1    Grotjahn, D.B.2
  • 402
    • 84893025319 scopus 로고    scopus 로고
    • Z-Selective Alkene Isomerization by High-Spin Cobalt(II) Complexes
    • Chen, C.; Dugan, T. R.; Brennessel, W. W.; Weix, D. J.; Holland, P. L. Z-Selective Alkene Isomerization by High-Spin Cobalt(II) Complexes J. Am. Chem. Soc. 2014, 136, 945-955 10.1021/ja408238n
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 945-955
    • Chen, C.1    Dugan, T.R.2    Brennessel, W.W.3    Weix, D.J.4    Holland, P.L.5
  • 403
    • 84944916851 scopus 로고    scopus 로고
    • Approach to cis-Phlegmarine Alkaloids via Stereodivergent Reduction: Total Synthesis of (+)-Serratezomine e and Putative Structure of (-)-Huperzine N
    • Bosch, C.; Fiser, B.; Gómez-Bengoa, E.; Bradshaw, B.; Bonjoch, J. Approach to cis-Phlegmarine Alkaloids via Stereodivergent Reduction: Total Synthesis of (+)-Serratezomine E and Putative Structure of (-)-Huperzine N Org. Lett. 2015, 17, 5084 10.1021/acs.orglett.5b02581
    • (2015) Org. Lett. , vol.17 , pp. 5084
    • Bosch, C.1    Fiser, B.2    Gómez-Bengoa, E.3    Bradshaw, B.4    Bonjoch, J.5
  • 404
    • 85027939403 scopus 로고    scopus 로고
    • Concise Construction of Bicyclo[6.4.0] and -[7.4.0] Frameworks by [4 + 2] Cycloaddition of 3,4-Dimethylene-2,5-bis(phenylsulfonyl)cycloalk-1-enes
    • Mukai, C.; Ueda, M.; Takahashi, Y.; Inagaki, F. Concise Construction of Bicyclo[6.4.0] and -[7.4.0] Frameworks by [4 + 2] Cycloaddition of 3,4-Dimethylene-2,5-bis(phenylsulfonyl)cycloalk-1-enes Eur. J. Org. Chem. 2015, 2015, 4412-4422 10.1002/ejoc.201500598
    • (2015) Eur. J. Org. Chem. , vol.2015 , pp. 4412-4422
    • Mukai, C.1    Ueda, M.2    Takahashi, Y.3    Inagaki, F.4
  • 405
    • 84975042668 scopus 로고    scopus 로고
    • Synthesis of (+)-7,20-Diisocyanoadociane and Liver Stage Antiplasmodial Activity of the ICT Class
    • Lu, H.-H.; Pronin, S. V.; Antonova-Koch, Y.; Meister, S.; Winzeler, E. A.; Shenvi, R. A. Synthesis of (+)-7,20-Diisocyanoadociane and Liver Stage Antiplasmodial Activity of the ICT Class J. Am. Chem. Soc. 2016, 138, 7268-7271 10.1021/jacs.6b03899
    • (2016) J. Am. Chem. Soc. , vol.138 , pp. 7268-7271
    • Lu, H.-H.1    Pronin, S.V.2    Antonova-Koch, Y.3    Meister, S.4    Winzeler, E.A.5    Shenvi, R.A.6
  • 406
    • 34347271804 scopus 로고    scopus 로고
    • Hydroformylation of Alkenes: An Industrial View of the Status and Importance
    • Bohnen, H.-W.; Cornils, B. Hydroformylation of Alkenes: An Industrial View of the Status and Importance Adv. Catal. 2002, 47, 1-64 10.1016/S0360-0564(02)47005-8
    • (2002) Adv. Catal. , vol.47 , pp. 1-64
    • Bohnen, H.-W.1    Cornils, B.2
  • 408
    • 0012316426 scopus 로고
    • The Brønsted acidity of Transition Metal Hydrides
    • Pearson, R. G.; Ford, P. C. The Brønsted acidity of Transition Metal Hydrides Comments Inorg. Chem. 1982, 1, 279-291 10.1080/02603598208078099
    • (1982) Comments Inorg. Chem. , vol.1 , pp. 279-291
    • Pearson, R.G.1    Ford, P.C.2
  • 409
    • 0002288783 scopus 로고
    • The Transition-Metal-Hydrogen Bond
    • Pearson, R. G. The Transition-Metal-Hydrogen Bond Chem. Rev. 1985, 85, 41-49 10.1021/cr00065a002
    • (1985) Chem. Rev. , vol.85 , pp. 41-49
    • Pearson, R.G.1
  • 410
    • 33845279086 scopus 로고
    • Seventeen-Electron Metal-Centered Radicals
    • Baird, M. C. Seventeen-Electron Metal-Centered Radicals Chem. Rev. 1988, 88, 1217-1227 10.1021/cr00089a011
    • (1988) Chem. Rev. , vol.88 , pp. 1217-1227
    • Baird, M.C.1
  • 411
    • 0042801932 scopus 로고
    • 4 and CO with Styrene. Mechanism of (a-Phenylpropionyl)- and (b-Phenylpropionyl)cobalt Tetracarbonyl Formation
    • 4 and CO with Styrene. Mechanism of (a-Phenylpropionyl)- and (b-Phenylpropionyl)cobalt Tetracarbonyl Formation Organometallics 1982, 1, 1120-1125 10.1021/om00069a003
    • (1982) Organometallics , vol.1 , pp. 1120-1125
    • Ungvary, F.1    Marko, L.2
  • 413
    • 0000592683 scopus 로고
    • 15N NMR Spectroscopic Studies of Lithium Dialkylamides. Solution Structure of Lithium Isopropylcyclohexylamide (LICA) in Tetrahydrofuran
    • 15N NMR Spectroscopic Studies of Lithium Dialkylamides. Solution Structure of Lithium Isopropylcyclohexylamide (LICA) in Tetrahydrofuran J. Am. Chem. Soc. 1988, 110, 2658-2660 10.1021/ja00216a055
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 2658-2660
    • Galiano-Roth, A.S.1    Michaelides, E.M.2    Collum, D.B.3
  • 414
    • 0346402113 scopus 로고
    • Free Radical Reactions of Tetracarbonylhydridocobalt
    • Nalesnik, T. E.; Orchin, M. Free Radical Reactions of Tetracarbonylhydridocobalt Organometallics 1982, 1, 222-223 10.1021/om00061a041
    • (1982) Organometallics , vol.1 , pp. 222-223
    • Nalesnik, T.E.1    Orchin, M.2
  • 415
    • 0000183581 scopus 로고
    • Acylcobalt Carbonyls and their Triphenylphosphine Complexes
    • Heck, R. F.; Breslow, D. S. Acylcobalt Carbonyls and their Triphenylphosphine Complexes J. Am. Chem. Soc. 1962, 84, 2499-2502 10.1021/ja00872a009
    • (1962) J. Am. Chem. Soc. , vol.84 , pp. 2499-2502
    • Heck, R.F.1    Breslow, D.S.2
  • 416
    • 33947478638 scopus 로고
    • The Reaction of Cobalt Hydrotetracarbonyl with Olefins
    • Heck, R. F.; Breslow, D. S. The Reaction of Cobalt Hydrotetracarbonyl with Olefins J. Am. Chem. Soc. 1961, 83, 4023-4027 10.1021/ja01480a017
    • (1961) J. Am. Chem. Soc. , vol.83 , pp. 4023-4027
    • Heck, R.F.1    Breslow, D.S.2
  • 417
    • 33845378340 scopus 로고
    • Synthesis and Chemistry of a Bridging Vinylidenedicobalt Complex. Evidence for a Nonchain Radical Mechanism in Its Reaction with Metal Hydrides to Give Heteronuclear Clusters
    • Jacobsen, E. N.; Bergman, R. G. Synthesis and Chemistry of a Bridging Vinylidenedicobalt Complex. Evidence for a Nonchain Radical Mechanism in Its Reaction with Metal Hydrides to Give Heteronuclear Clusters J. Am. Chem. Soc. 1985, 107, 2023-2032 10.1021/ja00293a037
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 2023-2032
    • Jacobsen, E.N.1    Bergman, R.G.2
  • 419
    • 0041523367 scopus 로고
    • 3, and Conjugated Dienes. Evidence for a Free Radical Mechanism
    • 3, and Conjugated Dienes. Evidence for a Free Radical Mechanism Organometallics 1984, 3, 1333-1337 10.1021/om00087a002
    • (1984) Organometallics , vol.3 , pp. 1333-1337
    • Connolly, J.W.1
  • 420
    • 0347452347 scopus 로고
    • The Hydrogenation of 9,10-Dimethylanthracene by Hydridopentacarbonylmanganese(I). Evidence for a Free-Radical Mechanism
    • Sweany, R.; Butler, S. C.; Halpern, J. The Hydrogenation of 9,10-Dimethylanthracene by Hydridopentacarbonylmanganese(I). Evidence for a Free-Radical Mechanism J. Organomet. Chem. 1981, 213, 487-492 10.1016/S0022-328X(00)82954-X
    • (1981) J. Organomet. Chem. , vol.213 , pp. 487-492
    • Sweany, R.1    Butler, S.C.2    Halpern, J.3
  • 423
    • 0001193406 scopus 로고
    • Relative Rates of H• Transfer from Transition-Metal Hydrides to Trityl Radicals
    • Eisenberg, D. C.; Lawrie, C. J.; Moody, A. E.; Norton, J. R. Relative Rates of H• Transfer from Transition-Metal Hydrides to Trityl Radicals J. Am. Chem. Soc. 1991, 113, 4888-4895 10.1021/ja00013a026
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 4888-4895
    • Eisenberg, D.C.1    Lawrie, C.J.2    Moody, A.E.3    Norton, J.R.4
  • 424
    • 34247515508 scopus 로고    scopus 로고
    • Large Ground-State Entropy Changes for Hydrogen Atom Transfer Reactions of Iron Complexes
    • Mader, E. A.; Davidson, E. R.; Mayer, J. M. Large Ground-State Entropy Changes for Hydrogen Atom Transfer Reactions of Iron Complexes J. Am. Chem. Soc. 2007, 129, 5153-5166 10.1021/ja0686918
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 5153-5166
    • Mader, E.A.1    Davidson, E.R.2    Mayer, J.M.3
  • 425
    • 33845282825 scopus 로고
    • Hydrogen Atom Transfer Reactions of Transition-Metal Hydrides. Utilization of a Radical Rearrangement in the Determination of Hydrogen Atom Transfer Rates
    • Bullock, R. M.; Samsel, E. G. Hydrogen Atom Transfer Reactions of Transition-Metal Hydrides. Utilization of a Radical Rearrangement in the Determination of Hydrogen Atom Transfer Rates J. Am. Chem. Soc. 1987, 109, 6542-6544 10.1021/ja00255a067
    • (1987) J. Am. Chem. Soc. , vol.109 , pp. 6542-6544
    • Bullock, R.M.1    Samsel, E.G.2
  • 426
    • 0000593804 scopus 로고
    • Hydrogen Atom Transfer Reactions of Transition-Metal Hydrides. Kinetics and Mechanism of the Hydrogenation of a-Cyclopropylstyrene by Metal Carbonyl Hydrides
    • Bullock, R. M.; Samsel, E. G. Hydrogen Atom Transfer Reactions of Transition-Metal Hydrides. Kinetics and Mechanism of the Hydrogenation of a-Cyclopropylstyrene by Metal Carbonyl Hydrides J. Am. Chem. Soc. 1990, 112, 6886-6898 10.1021/ja00175a024
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 6886-6898
    • Bullock, R.M.1    Samsel, E.G.2
  • 427
    • 0035901673 scopus 로고    scopus 로고
    • Factors Controlling the Addition of Carbon-Centered Radicals to Alkenes - An Experimental and Theoretical Perspective
    • Fischer, H.; Radom, L. Factors Controlling the Addition of Carbon-Centered Radicals to Alkenes-An Experimental and Theoretical Perspective Angew. Chem., Int. Ed. 2001, 40, 1340-1371 10.1002/1521-3773(20010417)40:8<1340::AID-ANIE1340>3.0.CO;2-#
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 1340-1371
    • Fischer, H.1    Radom, L.2
  • 428
    • 0022430394 scopus 로고
    • 12-Dependent Rearrangements
    • 12-Dependent Rearrangements Science 1985, 227, 869-875 10.1126/science.2857503
    • (1985) Science , vol.227 , pp. 869-875
    • Halpern, J.1
  • 430
    • 81255127888 scopus 로고    scopus 로고
    • Cobalt-Catalyzed Coupling of Alkyl Iodides with Alkenes: Deprotonation of Hydridocobalt Enables Turnover
    • Weiss, M. E.; Kreis, L. M.; Lauber, A.; Carreira, E. M. Cobalt-Catalyzed Coupling of Alkyl Iodides with Alkenes: Deprotonation of Hydridocobalt Enables Turnover Angew. Chem., Int. Ed. 2011, 50, 11125-11128 10.1002/anie.201105235
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 11125-11128
    • Weiss, M.E.1    Kreis, L.M.2    Lauber, A.3    Carreira, E.M.4
  • 431
    • 0011631587 scopus 로고
    • Autocatalytic Reduction of Pyridinecobaloxime(III) by Molecular Hydrogen
    • Szeverényi, Z.; Budó-Záhonyi, é.; Simándi, L. I. Autocatalytic Reduction of Pyridinecobaloxime(III) by Molecular Hydrogen J. Coord. Chem. 1980, 10, 41-45 10.1080/00958978008079849
    • (1980) J. Coord. Chem. , vol.10 , pp. 41-45
    • Szeverényi, Z.1    Budó-Záhonyi, É.2    Simándi, L.I.3
  • 434
  • 435
    • 0000197790 scopus 로고
    • Chemical Mechanism of Olefin Oxygenation Reaction Catalyzed by Bis(acetylacetonato)nikel(II) or Cobalt(II) Compounds in the Presence of Reducing Agents
    • Nishida, Y.; Tanaka, N.; Okazaki, M. Chemical Mechanism of Olefin Oxygenation Reaction Catalyzed by Bis(acetylacetonato)nikel(II) or Cobalt(II) Compounds in the Presence of Reducing Agents Polyhedron 1994, 13, 2245-2249 10.1016/S0277-5387(00)88131-0
    • (1994) Polyhedron , vol.13 , pp. 2245-2249
    • Nishida, Y.1    Tanaka, N.2    Okazaki, M.3
  • 436
    • 44949237920 scopus 로고    scopus 로고
    • Enantioselective Borohydride Reduction Catalyzed by Cobalt Complexes: Discovery, Analysis, and Design for a Halogen-Free System
    • Yamada, T. Enantioselective Borohydride Reduction Catalyzed by Cobalt Complexes: Discovery, Analysis, and Design for a Halogen-Free System Synthesis 2008, 2008, 1628-1640 10.1055/s-2008-1067036
    • (2008) Synthesis , vol.2008 , pp. 1628-1640
    • Yamada, T.1
  • 437
    • 0000604006 scopus 로고
    • Metal-Ammonia Reductions of Cyclic Aliphatic Ketones
    • Huffman, J. W. Metal-Ammonia Reductions of Cyclic Aliphatic Ketones Acc. Chem. Res. 1983, 16, 399-405 10.1021/ar00095a002
    • (1983) Acc. Chem. Res. , vol.16 , pp. 399-405
    • Huffman, J.W.1
  • 438
    • 0010811217 scopus 로고
    • Catalysis in Organosilicon Chemistry. III. Catalytic Mode, Solvent Isotope Effects, and Transition-State Structure in Hydride Expulsion from Silicon
    • O'Donnell, K.; Bacon, R.; Chellappa, K. L.; Schowen, R. L.; Lee, J. K. Catalysis in Organosilicon Chemistry. III. Catalytic Mode, Solvent Isotope Effects, and Transition-State Structure in Hydride Expulsion from Silicon J. Am. Chem. Soc. 1972, 94, 2500-2505 10.1021/ja00762a051
    • (1972) J. Am. Chem. Soc. , vol.94 , pp. 2500-2505
    • O'Donnell, K.1    Bacon, R.2    Chellappa, K.L.3    Schowen, R.L.4    Lee, J.K.5
  • 439
    • 84892371359 scopus 로고    scopus 로고
    • Base-Catalyzed Hydrosilylation of Ketones and Esters and Insight into the Mechanism
    • Revunova, K.; Nikonov, G. I. Base-Catalyzed Hydrosilylation of Ketones and Esters and Insight into the Mechanism Chem.-Eur. J. 2014, 20, 839-845 10.1002/chem.201302728
    • (2014) Chem. - Eur. J. , vol.20 , pp. 839-845
    • Revunova, K.1    Nikonov, G.I.2
  • 440
    • 84865120407 scopus 로고    scopus 로고
    • New Insights into the Mechanism and an Expanded Scope of the Fe(III)-Mediated Vinblastine Coupling Reaction
    • Gotoh, H.; Sears, J. E.; Eschenmoser, A.; Boger, D. L. New Insights into the Mechanism and an Expanded Scope of the Fe(III)-Mediated Vinblastine Coupling Reaction J. Am. Chem. Soc. 2012, 134, 13240-13243 10.1021/ja306229x
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 13240-13243
    • Gotoh, H.1    Sears, J.E.2    Eschenmoser, A.3    Boger, D.L.4
  • 441
    • 33845379500 scopus 로고
    • Cobalt(III) Alkylperoxy Complexes. Synthesis, X-Ray Structure, and Role in the Catalytic Decomposition of Alkyl Hydroperoxides and in the Hydroxylation of Hydrocarbons
    • Saussine, L.; Brazi, E.; Robine, A.; Mimoun, H.; Fischer, J.; Weiss, R. Cobalt(III) Alkylperoxy Complexes. Synthesis, X-Ray Structure, and Role in the Catalytic Decomposition of Alkyl Hydroperoxides and in the Hydroxylation of Hydrocarbons J. Am. Chem. Soc. 1985, 107, 3534-3540 10.1021/ja00298a022
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 3534-3540
    • Saussine, L.1    Brazi, E.2    Robine, A.3    Mimoun, H.4    Fischer, J.5    Weiss, R.6
  • 442
    • 0001723715 scopus 로고
    • Stereochemistry and Mechanism of the Photochemical and Thermal Insertion of Oxygen into the Carbon-Cobalt Bond of Alkyl(pyridine)cobaloximes
    • Jensen, F. R.; Kiskis, R. C. Stereochemistry and Mechanism of the Photochemical and Thermal Insertion of Oxygen into the Carbon-Cobalt Bond of Alkyl(pyridine)cobaloximes J. Am. Chem. Soc. 1975, 97, 5825-5831 10.1021/ja00853a029
    • (1975) J. Am. Chem. Soc. , vol.97 , pp. 5825-5831
    • Jensen, F.R.1    Kiskis, R.C.2
  • 445
    • 0035903932 scopus 로고    scopus 로고
    • 3 Catalyst and Phenylsilane in the Presence of Dioxygen
    • 3 Catalyst and Phenylsilane in the Presence of Dioxygen Tetrahedron Lett. 2001, 42, 6633-6636 10.1016/S0040-4039(01)01304-1
    • (2001) Tetrahedron Lett. , vol.42 , pp. 6633-6636
    • Magnus, P.1    Fielding, M.R.2
  • 446
    • 0009161210 scopus 로고
    • Reduction of Olefins Using Sodium-Hexamethylphosphoramide-Tert-Butyl Alcohol
    • Whitesides, G. M.; Ehmann, W. J. Reduction of Olefins Using Sodium-Hexamethylphosphoramide-Tert-Butyl Alcohol J. Org. Chem. 1970, 35, 3565-3567 10.1021/jo00835a087
    • (1970) J. Org. Chem. , vol.35 , pp. 3565-3567
    • Whitesides, G.M.1    Ehmann, W.J.2
  • 447
    • 0001214791 scopus 로고
    • Bridgehead Decalin Radicals: Evidence for Nonplanarity at the Radical Site
    • Lloyd, R. V.; Williams, R. V. Bridgehead Decalin Radicals: Evidence for Nonplanarity at the Radical Site J. Phys. Chem. 1985, 89, 5379-5381 10.1021/j100271a013
    • (1985) J. Phys. Chem. , vol.89 , pp. 5379-5381
    • Lloyd, R.V.1    Williams, R.V.2
  • 448
    • 0000829322 scopus 로고
    • Organosilanes as Radical-Based Reducing Agents in Synthesis
    • Chatgilialoglu, C. Organosilanes as Radical-Based Reducing Agents in Synthesis Acc. Chem. Res. 1992, 25, 188-194 10.1021/ar00016a003
    • (1992) Acc. Chem. Res. , vol.25 , pp. 188-194
    • Chatgilialoglu, C.1
  • 449
    • 4243749358 scopus 로고
    • Structural and Chemical Properties of Silyl Radicals
    • Chatgilialoglu, C. Structural and Chemical Properties of Silyl Radicals Chem. Rev. 1995, 95, 1229-1251 10.1021/cr00037a005
    • (1995) Chem. Rev. , vol.95 , pp. 1229-1251
    • Chatgilialoglu, C.1
  • 450
    • 78751499421 scopus 로고    scopus 로고
    • Understanding Hydrogen Atom Transfer: From Bond Strengths to Marcus Theory
    • Mayer, J. M. Understanding Hydrogen Atom Transfer: From Bond Strengths to Marcus Theory Acc. Chem. Res. 2011, 44, 36-46 10.1021/ar100093z
    • (2011) Acc. Chem. Res. , vol.44 , pp. 36-46
    • Mayer, J.M.1
  • 451
    • 84858776560 scopus 로고    scopus 로고
    • On the Interpretation of Deuterium Kinetic Isotope Effects in C-H Bond Functionalizations by Transition-Metal Complexes
    • Simmons, E. M.; Hartwig, J. F. On the Interpretation of Deuterium Kinetic Isotope Effects in C-H Bond Functionalizations by Transition-Metal Complexes Angew. Chem., Int. Ed. 2012, 51, 3066-3072 10.1002/anie.201107334
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 3066-3072
    • Simmons, E.M.1    Hartwig, J.F.2
  • 452
    • 0035780989 scopus 로고    scopus 로고
    • Catalytic Chain Transfer in Free-Radical Polymerizations
    • Gridnev, A. A.; Ittel, S. D. Catalytic Chain Transfer in Free-Radical Polymerizations Chem. Rev. 2001, 101, 3611-3660 10.1021/cr9901236
    • (2001) Chem. Rev. , vol.101 , pp. 3611-3660
    • Gridnev, A.A.1    Ittel, S.D.2
  • 453
    • 84923787935 scopus 로고
    • Living Radical Polymerization of Acrylates by Organocobalt Porphyrin Complexes
    • Wayland, B. B.; Poszmik, G.; Mukerjee, S. L.; Fryd, M. Living Radical Polymerization of Acrylates by Organocobalt Porphyrin Complexes J. Am. Chem. Soc. 1994, 116, 7943-7944 10.1021/ja00096a080
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 7943-7944
    • Wayland, B.B.1    Poszmik, G.2    Mukerjee, S.L.3    Fryd, M.4
  • 454
    • 53549135236 scopus 로고    scopus 로고
    • Exchange of Organic Radicals with Organo-Cobalt Complexes Formed in the Living Radical Polymerization of Vinyl Acetate
    • Li, S.; de Bruin, B.; Peng, C.-H.; Fryd, M.; Wayland, B. B. Exchange of Organic Radicals with Organo-Cobalt Complexes Formed in the Living Radical Polymerization of Vinyl Acetate J. Am. Chem. Soc. 2008, 130, 13373-13381 10.1021/ja804010h
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 13373-13381
    • Li, S.1    De Bruin, B.2    Peng, C.-H.3    Fryd, M.4    Wayland, B.B.5
  • 455
    • 65349159157 scopus 로고    scopus 로고
    • Hydrogen-Atom Transfer in Reactions of Organic Radicals with [Co(II) (por)]· (Por = Porphyrinato) and in Subsequent Addition of [Co(H) (por)] to Olefins
    • De Bruin, B.; Dzik, W. I.; Li, S.; Wayland, B. B. Hydrogen-Atom Transfer in Reactions of Organic Radicals with [Co(II) (por)]· (Por = Porphyrinato) and in Subsequent Addition of [Co(H) (por)] to Olefins Chem.-Eur. J. 2009, 15, 4312-4320 10.1002/chem.200802022
    • (2009) Chem. - Eur. J. , vol.15 , pp. 4312-4320
    • De Bruin, B.1    Dzik, W.I.2    Li, S.3    Wayland, B.B.4
  • 456
    • 0036128645 scopus 로고    scopus 로고
    • Atom Transfer Radical Cyclisation Reactions Mediated by Copper Complexes
    • Clark, A. J. Atom Transfer Radical Cyclisation Reactions Mediated by Copper Complexes Chem. Soc. Rev. 2002, 31, 1-11 10.1039/b107811a
    • (2002) Chem. Soc. Rev. , vol.31 , pp. 1-11
    • Clark, A.J.1
  • 458
    • 84856630050 scopus 로고    scopus 로고
    • Iron Catalysts for Selective Anti-Markovnikov Alkene Hydrosilylation Using Tertiary Silanes
    • Tondreau, A. M.; Atienza, C. C. H.; Weller, K. J.; Nye, S. A.; Lewis, K. M.; Delis, J. G. P.; Chirik, P. J. Iron Catalysts for Selective Anti-Markovnikov Alkene Hydrosilylation Using Tertiary Silanes Science 2012, 335, 567-570 10.1126/science.1214451
    • (2012) Science , vol.335 , pp. 567-570
    • Tondreau, A.M.1    Atienza, C.C.H.2    Weller, K.J.3    Nye, S.A.4    Lewis, K.M.5    Delis, J.G.P.6    Chirik, P.J.7
  • 461
    • 0001728539 scopus 로고
    • Formation of C-C Bonds by Addition of Free Radicals to Alkenes
    • Giese, B. Formation of C-C Bonds by Addition of Free Radicals to Alkenes Angew. Chem., Int. Ed. Engl. 1983, 22, 753-764 10.1002/anie.198307531
    • (1983) Angew. Chem., Int. Ed. Engl. , vol.22 , pp. 753-764
    • Giese, B.1
  • 462
    • 0001180629 scopus 로고
    • Rate Constants for Some Prototype Radical Reactions in Liquids by Kinetic Electron Spin Resonance
    • Fischer, H.; Paul, H. Rate Constants for Some Prototype Radical Reactions in Liquids by Kinetic Electron Spin Resonance Acc. Chem. Res. 1987, 20, 200-206 10.1021/ar00137a007
    • (1987) Acc. Chem. Res. , vol.20 , pp. 200-206
    • Fischer, H.1    Paul, H.2
  • 463
    • 0037077603 scopus 로고    scopus 로고
    • Factors Affecting the Rates of Addition of Free Radicals to Alkenes. Determination of Absolute Rate Coefficients Using the Persistent Aminoxyl Method
    • Beckwith, A. L. J.; Poole, J. S. Factors Affecting the Rates of Addition of Free Radicals to Alkenes. Determination of Absolute Rate Coefficients Using the Persistent Aminoxyl Method J. Am. Chem. Soc. 2002, 124, 9489-9497 10.1021/ja025730g
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 9489-9497
    • Beckwith, A.L.J.1    Poole, J.S.2
  • 464
    • 0026561946 scopus 로고
    • The Invention of Radical Reactions. Part XXIII New Reactions: Nitrile and Thiocyanate Transfer to Carbon Radicals from Sulfonyl Cyanides and Sulfonyl Isothiocyanates
    • Barton, D. H. R.; Jaszberenyi, J. C.; Theodorakis, E. A. The Invention of Radical Reactions. Part XXIII New Reactions: Nitrile and Thiocyanate Transfer to Carbon Radicals from Sulfonyl Cyanides and Sulfonyl Isothiocyanates Tetrahedron 1992, 48, 2613-2626 10.1016/S0040-4020(01)88524-0
    • (1992) Tetrahedron , vol.48 , pp. 2613-2626
    • Barton, D.H.R.1    Jaszberenyi, J.C.2    Theodorakis, E.A.3
  • 465
    • 33845282341 scopus 로고
    • A Force-Field Model for Intramolecular Radical Additions
    • Spellmeyer, D. C.; Houk, K. N. A Force-Field Model for Intramolecular Radical Additions J. Org. Chem. 1987, 52, 959-974 10.1021/jo00382a001
    • (1987) J. Org. Chem. , vol.52 , pp. 959-974
    • Spellmeyer, D.C.1    Houk, K.N.2
  • 466
    • 0039785339 scopus 로고    scopus 로고
    • Toward an Alkene Hydroamination Catalyst: Static and Dynamic Ab Initio DFT Studies
    • Senn, H. M.; Blöchl, P. E.; Togni, A. Toward an Alkene Hydroamination Catalyst: Static and Dynamic Ab Initio DFT Studies J. Am. Chem. Soc. 2000, 122, 4098-4107 10.1021/ja992689h
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 4098-4107
    • Senn, H.M.1    Blöchl, P.E.2    Togni, A.3
  • 467
    • 33947468395 scopus 로고
    • Reactions of Atoms and Free Radicals in Solution. XXXIX. The Reaction of Diacetyl Peroxide with Sec-Butyl Nitrite and 3-Amyl Nitrite
    • Kharasch, M. S.; Meltzer, T. H.; Nudenberg, W. Reactions of Atoms and Free Radicals in Solution. XXXIX. The Reaction of Diacetyl Peroxide with Sec-Butyl Nitrite and 3-Amyl Nitrite J. Org. Chem. 1957, 22, 37-39 10.1021/jo01352a008
    • (1957) J. Org. Chem. , vol.22 , pp. 37-39
    • Kharasch, M.S.1    Meltzer, T.H.2    Nudenberg, W.3
  • 468
    • 84986384468 scopus 로고
    • Deoxygenation of Nitro and Nitrosoaromatics by Photolysis with t-BuHgl/Kl. Regiochemistry Oftert-Butyl Radical Addition to Nitrosoaromatics
    • Russell, G. A.; Yao, C.-F. Deoxygenation of Nitro and Nitrosoaromatics by Photolysis With t-BuHgl/Kl. Regiochemistry Oftert-Butyl Radical Addition to Nitrosoaromatics Heteroat. Chem. 1993, 4, 433-444 10.1002/hc.520040505
    • (1993) Heteroat. Chem. , vol.4 , pp. 433-444
    • Russell, G.A.1    Yao, C.-F.2
  • 469
    • 0009058518 scopus 로고
    • Mechanism of a Novel Synthesis of Haemin c from Protohaemin and L-Cysteine. A Markownikoff-Type Radical Addition Reaction
    • Kojo, S.; Sano, S. Mechanism of a Novel Synthesis of Haemin c from Protohaemin and L-Cysteine. A Markownikoff-Type Radical Addition Reaction J. Chem. Soc., Perkin Trans. 1 1981, 2864-2870 10.1039/p19810002864
    • (1981) J. Chem. Soc., Perkin Trans. 1 , pp. 2864-2870
    • Kojo, S.1    Sano, S.2
  • 470
    • 71949099030 scopus 로고    scopus 로고
    • Synthesis, Properties, and Reactivity of Diketiminate-Supported Cobalt Fluoride Complexes
    • Ding, K.; Dugan, T. R.; Brennessel, W. W.; Bill, E.; Holland, P. L. Synthesis, Properties, and Reactivity of Diketiminate-Supported Cobalt Fluoride Complexes Organometallics 2009, 28, 6650-6656 10.1021/om900394t
    • (2009) Organometallics , vol.28 , pp. 6650-6656
    • Ding, K.1    Dugan, T.R.2    Brennessel, W.W.3    Bill, E.4    Holland, P.L.5
  • 471
    • 0037077589 scopus 로고    scopus 로고
    • 2 -Silane (Dpm = 2,2,6,6-Tetramethylheptane-3,5-Dionate): Mechanism and Partitioning of Hydrometallative versus Anion Radical Pathways
    • 2 -Silane (Dpm = 2,2,6,6-Tetramethylheptane-3,5-Dionate): Mechanism and Partitioning of Hydrometallative versus Anion Radical Pathways J. Am. Chem. Soc. 2002, 124, 9448-9453 10.1021/ja020223k
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 9448-9453
    • Wang, L.-C.1    Jang, H.-Y.2    Roh, Y.3    Lynch, V.4    Schultz, A.J.5    Wang, X.6    Krische, M.J.7
  • 472
    • 0034803563 scopus 로고    scopus 로고
    • Catalytic Dehydrogenative Coupling of Secondary Silanes Using Wilkinson's Catalyst
    • Rosenberg, L.; Davis, C. W.; Yao, J. Catalytic Dehydrogenative Coupling of Secondary Silanes Using Wilkinson's Catalyst J. Am. Chem. Soc. 2001, 123, 5120-5121 10.1021/ja015697i
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 5120-5121
    • Rosenberg, L.1    Davis, C.W.2    Yao, J.3
  • 473
    • 33947490919 scopus 로고
    • Homogeneous Catalysis. II. the Mechanism of the Hydrosilation of Olefins Catalyzed by Group VIII Metal Complexes
    • Chalk, A. J.; Harrod, J. F. Homogeneous Catalysis. II. The Mechanism of the Hydrosilation of Olefins Catalyzed by Group VIII Metal Complexes J. Am. Chem. Soc. 1965, 87, 16-21 10.1021/ja01079a004
    • (1965) J. Am. Chem. Soc. , vol.87 , pp. 16-21
    • Chalk, A.J.1    Harrod, J.F.2
  • 474
    • 0000426857 scopus 로고
    • Formation and Oxidation of Alkyl Radicals by Cobalt(III) Complexes
    • Lande, S. S.; Kochi, J. K. Formation and Oxidation of Alkyl Radicals by Cobalt(III) Complexes J. Am. Chem. Soc. 1968, 90, 5196-5207 10.1021/ja01021a023
    • (1968) J. Am. Chem. Soc. , vol.90 , pp. 5196-5207
    • Lande, S.S.1    Kochi, J.K.2
  • 475
    • 33751331898 scopus 로고    scopus 로고
    • Computational Studies of Metal-Ligand Bond Enthalpies across the Transition Metal Series
    • Uddin, J.; Morales, C. M.; Maynard, J. H.; Landis, C. R. Computational Studies of Metal-Ligand Bond Enthalpies across the Transition Metal Series Organometallics 2006, 25, 5566-5581 10.1021/om0603058
    • (2006) Organometallics , vol.25 , pp. 5566-5581
    • Uddin, J.1    Morales, C.M.2    Maynard, J.H.3    Landis, C.R.4
  • 476
    • 77955397974 scopus 로고    scopus 로고
    • Probing a Biomimetic Approach to Mycaperoxide B: Hydroperoxidation Studies
    • Harwood, L.; Silva, E.; Pye, R.; Cardin, C. Probing a Biomimetic Approach to Mycaperoxide B: Hydroperoxidation Studies Synlett 2010, 4, 509-513 10.1055/s-0029-1219152
    • (2010) Synlett , vol.4 , pp. 509-513
    • Harwood, L.1    Silva, E.2    Pye, R.3    Cardin, C.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.