메뉴 건너뛰기




Volumn 47, Issue 10, 2014, Pages 3162-3173

Anionic chiral tridentate n-donor pincer ligands in asymmetric catalysis

Author keywords

[No Author keywords available]

Indexed keywords


EID: 84908093673     PISSN: 00014842     EISSN: 15204898     Source Type: Journal    
DOI: 10.1021/ar5002457     Document Type: Article
Times cited : (93)

References (95)
  • 6
    • 0035886138 scopus 로고    scopus 로고
    • Platinum Group Organometallics Based on "pincer" Complexes: Sensors, Switches, and Catalysts
    • Albrecht, M.; van Koten, G. Platinum Group Organometallics Based on "Pincer" Complexes: Sensors, Switches, and Catalysts Angew. Chem., Int. Ed. 2001, 40, 3750-3781
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 3750-3781
    • Albrecht, M.1    Van Koten, G.2
  • 7
    • 0038620356 scopus 로고    scopus 로고
    • Cyclometalated Phosphine-Based Pincer Complexes: Mechanistic Insight in Catalysis, Coordination, and Bond Activation
    • van der Boom, M.; Milstein, D. Cyclometalated Phosphine-Based Pincer Complexes: Mechanistic Insight in Catalysis, Coordination, and Bond Activation Chem. Rev. 2003, 103, 1759-1792
    • (2003) Chem. Rev. , vol.103 , pp. 1759-1792
    • Van Der Boom, M.1    Milstein, D.2
  • 9
    • 84868528156 scopus 로고    scopus 로고
    • Eds. Topics in Organometallic Chemistry, Vol. Springer: New York
    • Organometallic Pincer Chemistry; van Koten, G.; Milstein, D., Eds.; Topics in Organometallic Chemistry, Vol. 40; Springer: New York, 2013.
    • (2013) Organometallic Pincer Chemistry , vol.40
    • Van Koten, G.1    Milstein, D.2
  • 10
    • 0043240876 scopus 로고    scopus 로고
    • Pyridine-2,6-bis(oxazolines), Helpful Ligands for Asymmetric Catalysts
    • Desimoni, G.; Faita, G.; Quadrelli, P. Pyridine-2,6-bis(oxazolines), Helpful Ligands for Asymmetric Catalysts Chem. Rev. 2003, 103, 3119-3154
    • (2003) Chem. Rev. , vol.103 , pp. 3119-3154
    • Desimoni, G.1    Faita, G.2    Quadrelli, P.3
  • 11
    • 33749828310 scopus 로고    scopus 로고
    • 2-Symmetric Chiral Bis(oxazoline) Ligands in Asymmetric Catalysis
    • 2-Symmetric Chiral Bis(oxazoline) Ligands in Asymmetric Catalysis Chem. Rev. 2006, 106, 3561-3651
    • (2006) Chem. Rev. , vol.106 , pp. 3561-3651
    • Desimoni, G.1    Faita, G.2    Jørgensen, K.A.3
  • 12
    • 84908103025 scopus 로고    scopus 로고
    • Chem. Rev. 2012, 112, PR284-PR437.
    • (2012) Chem. Rev. , vol.112 , pp. 284-PR437
  • 13
    • 1542398427 scopus 로고    scopus 로고
    • Cyclopropanation with Diazomethane and Bis(oxazoline)palladium(II) Complexes
    • Denmark, S. E.; Stavenger, R. A.; Faucher, A.-M.; Edwards, J. P. Cyclopropanation with Diazomethane and Bis(oxazoline)palladium(II) Complexes J. Org. Chem. 1997, 62, 3375-3389
    • (1997) J. Org. Chem. , vol.62 , pp. 3375-3389
    • Denmark, S.E.1    Stavenger, R.A.2    Faucher, A.-M.3    Edwards, J.P.4
  • 15
    • 34250630793 scopus 로고    scopus 로고
    • Synthesis and use of bisoxazolinyl-phenyl pincers
    • Nishiyama, H. Synthesis and use of bisoxazolinyl-phenyl pincers Chem. Soc. Rev. 2007, 36, 1133-1141
    • (2007) Chem. Soc. Rev. , vol.36 , pp. 1133-1141
    • Nishiyama, H.1
  • 16
    • 0035216968 scopus 로고    scopus 로고
    • Development of the First P-Stereogenic PCP Pincer Ligands, Their Metallation by Palladium and Platinum, and Preliminary Catalysis
    • Williams, B. S.; Dani, P.; Lutz, M.; Spek, A. L.; van Koten, G. Development of the First P-Stereogenic PCP Pincer Ligands, Their Metallation by Palladium and Platinum, and Preliminary Catalysis Helv. Chim. Acta 2001, 84, 3519-3530
    • (2001) Helv. Chim. Acta , vol.84 , pp. 3519-3530
    • Williams, B.S.1    Dani, P.2    Lutz, M.3    Spek, A.L.4    Van Koten, G.5
  • 17
    • 33644915811 scopus 로고    scopus 로고
    • The first pincer-aryl [M-(NCN)] complexes {M = Pd(II); Pt(II)} with chiral pyridine donors: Synthesis and catalytic activity in C-C bond formation
    • Soro, B.; Stoccoro, S.; Minghetti, G.; Zucca, A.; Cinellu, M. A.; Manassero, M.; Gladiali, S. The first pincer-aryl [M-(NCN)] complexes {M = Pd(II); Pt(II)} with chiral pyridine donors: Synthesis and catalytic activity in C-C bond formation Inorg. Chim. Acta 2006, 359, 1879-1888
    • (2006) Inorg. Chim. Acta , vol.359 , pp. 1879-1888
    • Soro, B.1    Stoccoro, S.2    Minghetti, G.3    Zucca, A.4    Cinellu, M.A.5    Manassero, M.6    Gladiali, S.7
  • 18
    • 33847089947 scopus 로고
    • Grignard-type carbonyl addition of allyl halides by means of chromous salt. A chemospecific synthesis of homoallyl alcohols
    • Okude, Y.; Hirano, S.; Hiyama, T.; Nozaki, H. Grignard-type carbonyl addition of allyl halides by means of chromous salt. A chemospecific synthesis of homoallyl alcohols J. Am. Chem. Soc. 1977, 99, 3179-3181
    • (1977) J. Am. Chem. Soc. , vol.99 , pp. 3179-3181
    • Okude, Y.1    Hirano, S.2    Hiyama, T.3    Nozaki, H.4
  • 20
    • 0037486826 scopus 로고    scopus 로고
    • Carbon-Carbon Bond Formations Involving Organochromium(III) Reagents
    • Fürstner, A. Carbon-Carbon Bond Formations Involving Organochromium(III) Reagents Chem. Rev. 1999, 99, 991-1046
    • (1999) Chem. Rev. , vol.99 , pp. 991-1046
    • Fürstner, A.1
  • 21
    • 0032954123 scopus 로고    scopus 로고
    • Recent Advances in Chromium(II)- and Chromium(III)-Mediated Organic Synthesis
    • Wessjohann, L. A.; Scheid, G. Recent Advances in Chromium(II)- and Chromium(III)-Mediated Organic Synthesis Synthesis 1999, 1-36
    • (1999) Synthesis , pp. 1-36
    • Wessjohann, L.A.1    Scheid, G.2
  • 23
    • 0030458468 scopus 로고    scopus 로고
    • Nozaki-Hiyama-Kishi Reactions Catalytic in Chromium
    • Fürstner, A.; Shi, N. Nozaki-Hiyama-Kishi Reactions Catalytic in Chromium J. Am. Chem. Soc. 1996, 118, 12349-12357
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 12349-12357
    • Fürstner, A.1    Shi, N.2
  • 24
    • 0037419886 scopus 로고    scopus 로고
    • Asymmetric Catalysis of Nozaki-Hiyama Allylation and Methallylation with a New Tridentate Bis(oxazolinyl)carbazole Ligand
    • Inoue, M.; Suzuki, T.; Nakada, M. Asymmetric Catalysis of Nozaki-Hiyama Allylation and Methallylation with a New Tridentate Bis(oxazolinyl)carbazole Ligand J. Am. Chem. Soc. 2003, 125, 1140-1141
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 1140-1141
    • Inoue, M.1    Suzuki, T.2    Nakada, M.3
  • 25
    • 0037239928 scopus 로고    scopus 로고
    • A New Asymmetric Tridentate Carbazole Ligand: Its Preparation and Application to Nozaki-Hiyama Allylation
    • Suzuki, T.; Kinoshita, A.; Kawada, H.; Nakada, M. A New Asymmetric Tridentate Carbazole Ligand: Its Preparation and Application to Nozaki-Hiyama Allylation Synlett 2003, 570-572
    • (2003) Synlett , pp. 570-572
    • Suzuki, T.1    Kinoshita, A.2    Kawada, H.3    Nakada, M.4
  • 26
    • 34547830827 scopus 로고    scopus 로고
    • New Preparation of Tridentate Bis-oxazoline Carbazole Ligand Effective for Enantioselective Nozaki-Hiyama Reaction
    • Inoue, M.; Nakada, M. New Preparation of Tridentate Bis-oxazoline Carbazole Ligand Effective for Enantioselective Nozaki-Hiyama Reaction Heterocycles 2007, 72, 133-138
    • (2007) Heterocycles , vol.72 , pp. 133-138
    • Inoue, M.1    Nakada, M.2
  • 27
    • 77956382088 scopus 로고    scopus 로고
    • Enantioselective synthesis of butadien-2-ylcarbinols via (silylmethyl)allenic alcohols from chromium-catalyzed additions to aldehydes utilizing chiral carbazole ligands
    • Durán-Galván, M.; Worlikar, S. A.; Connell, B. T. Enantioselective synthesis of butadien-2-ylcarbinols via (silylmethyl)allenic alcohols from chromium-catalyzed additions to aldehydes utilizing chiral carbazole ligands Tetrahedron 2010, 66, 7707-7719
    • (2010) Tetrahedron , vol.66 , pp. 7707-7719
    • Durán-Galván, M.1    Worlikar, S.A.2    Connell, B.T.3
  • 28
    • 0037195663 scopus 로고    scopus 로고
    • Coupling of Bulky, Electron-Deficient Partners in Aryl Amination in the Preparation of Tridentate Bis(oxazoline) Ligands for Asymmetric Catalysis
    • McManus, H. A.; Guiry, P. J. Coupling of Bulky, Electron-Deficient Partners in Aryl Amination in the Preparation of Tridentate Bis(oxazoline) Ligands for Asymmetric Catalysis J. Org. Chem. 2002, 67, 8566-8573
    • (2002) J. Org. Chem. , vol.67 , pp. 8566-8573
    • McManus, H.A.1    Guiry, P.J.2
  • 29
    • 7444242815 scopus 로고    scopus 로고
    • 2-symmetric tridentate bis(thiazoline) and bis(oxazoline) ligands and their application in the enantioselective Henry reaction
    • 2-symmetric tridentate bis(thiazoline) and bis(oxazoline) ligands and their application in the enantioselective Henry reaction Tetrahedron: Asymmetry 2004, 15, 3433-3441
    • (2004) Tetrahedron: Asymmetry , vol.15 , pp. 3433-3441
    • Lu, S.-F.1    Du, D.-M.2    Zhang, S.-W.3    Xu, J.4
  • 30
    • 33645923054 scopus 로고    scopus 로고
    • Application of Tridentate Bis(oxazoline) Ligands in Catalytic Asymmetric Nozaki-Hiyama Allylation and Crotylation: An Example of High Enantioselection with a Non-Symmetric Bis(oxazoline) Ligand
    • McManus, H. A.; Cozzi, P. G.; Guiry, P. J. Application of Tridentate Bis(oxazoline) Ligands in Catalytic Asymmetric Nozaki-Hiyama Allylation and Crotylation: An Example of High Enantioselection with a Non-Symmetric Bis(oxazoline) Ligand Adv. Synth. Catal. 2006, 348, 551-558
    • (2006) Adv. Synth. Catal. , vol.348 , pp. 551-558
    • McManus, H.A.1    Cozzi, P.G.2    Guiry, P.J.3
  • 31
    • 33847221045 scopus 로고    scopus 로고
    • The application of bis(oxazoline) ligands in the catalytic enantioselective methallylation of aldehydes
    • Hargaden, G. C.; McManus, H. A.; Cozzi, P. G.; Guiry, P. J. The application of bis(oxazoline) ligands in the catalytic enantioselective methallylation of aldehydes Org. Biomol. Chem. 2007, 5, 763-766
    • (2007) Org. Biomol. Chem. , vol.5 , pp. 763-766
    • Hargaden, G.C.1    McManus, H.A.2    Cozzi, P.G.3    Guiry, P.J.4
  • 32
    • 83755172583 scopus 로고    scopus 로고
    • The Synthesis of a New Class of Chiral Pincer Ligands and Their Applications in Enantioselective Catalytic Fluorinations and the Nozaki-Hiyama-Kishi Reaction
    • Deng, Q.-H.; Wadepohl, H.; Gade, L. H. The Synthesis of a New Class of Chiral Pincer Ligands and Their Applications in Enantioselective Catalytic Fluorinations and the Nozaki-Hiyama-Kishi Reaction Chem.-Eur. J. 2011, 17, 14922-14928
    • (2011) Chem.-Eur. J. , vol.17 , pp. 14922-14928
    • Deng, Q.-H.1    Wadepohl, H.2    Gade, L.H.3
  • 33
    • 34247104647 scopus 로고    scopus 로고
    • Structure Elucidation and Enantioselective Total Synthesis of the Potent HMG-CoA Reductase Inhibitor FR901512 via Catalytic Asymmetric Nozaki-Hiyama Reactions
    • Inoue, M.; Nakada, M. Structure Elucidation and Enantioselective Total Synthesis of the Potent HMG-CoA Reductase Inhibitor FR901512 via Catalytic Asymmetric Nozaki-Hiyama Reactions J. Am. Chem. Soc. 2007, 129, 4164-4165
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 4164-4165
    • Inoue, M.1    Nakada, M.2
  • 34
    • 4444351226 scopus 로고    scopus 로고
    • Studies on Catalytic Asymmetric Nozaki-Hiyama Propargylation
    • Inoue, M.; Nakada, M. Studies on Catalytic Asymmetric Nozaki-Hiyama Propargylation Org. Lett. 2004, 6, 2977-2980
    • (2004) Org. Lett. , vol.6 , pp. 2977-2980
    • Inoue, M.1    Nakada, M.2
  • 35
    • 0034832840 scopus 로고    scopus 로고
    • Lewis Base Activation of Lewis Acids: Catalytic Enantioselective Allylation and Propargylation of Aldehydes
    • Denmark, S. E.; Wynn, T. Lewis Base Activation of Lewis Acids: Catalytic Enantioselective Allylation and Propargylation of Aldehydes J. Am. Chem. Soc. 2001, 123, 6199-6200
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 6199-6200
    • Denmark, S.E.1    Wynn, T.2
  • 36
    • 29544452399 scopus 로고    scopus 로고
    • Studies into Asymmetric Catalysis of the Nozaki-Hiyama Allenylation
    • Inoue, M.; Nakada, M. Studies into Asymmetric Catalysis of the Nozaki-Hiyama Allenylation Angew. Chem., Int. Ed. 2006, 45, 252-255
    • (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 252-255
    • Inoue, M.1    Nakada, M.2
  • 37
    • 77951157256 scopus 로고    scopus 로고
    • Asymmetric Synthesis of (1,3-Butadien-2-yl)methanols from Aldehydes via [1-(Silylmethyl)allenyl]methanols
    • Duran-Galvan, M.; Connell, B. T. Asymmetric Synthesis of (1,3-Butadien-2-yl)methanols from Aldehydes via [1-(Silylmethyl)allenyl]methanols Eur. J. Org. Chem. 2010, 2455-2488
    • (2010) Eur. J. Org. Chem. , pp. 2455-2488
    • Duran-Galvan, M.1    Connell, B.T.2
  • 38
    • 70449574094 scopus 로고    scopus 로고
    • First Regio- and Enantioselective Chromium-Catalyzed Homoallenylation of Aldehydes
    • Coeffard, V.; Aylward, M.; Guiry, P. J. First Regio- and Enantioselective Chromium-Catalyzed Homoallenylation of Aldehydes Angew. Chem., Int. Ed. 2009, 48, 9152-9155
    • (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 9152-9155
    • Coeffard, V.1    Aylward, M.2    Guiry, P.J.3
  • 42
    • 27144518078 scopus 로고    scopus 로고
    • Catalytic Enantioselective Friedel-Crafts Alkylation of Indoles with Nitroalkenes by Using a Simple Thiourea Organocatalyst
    • Herrera, R. P.; Sgarzani, V.; Bernardi, L.; Ricci, A. Catalytic Enantioselective Friedel-Crafts Alkylation of Indoles with Nitroalkenes by Using a Simple Thiourea Organocatalyst Angew. Chem., Int. Ed. 2005, 44, 6576-6579
    • (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 6576-6579
    • Herrera, R.P.1    Sgarzani, V.2    Bernardi, L.3    Ricci, A.4
  • 43
    • 23044472914 scopus 로고    scopus 로고
    • Enantioselective Friedel-Crafts type addition of indoles to nitro-olefins using a chiral hydrogen-bonding catalyst-Synthesis of optically active tetrahydro-β-carbolines
    • Zhuang, W.; Hazell, R. G.; Jørgensen, K. A. Enantioselective Friedel-Crafts type addition of indoles to nitro-olefins using a chiral hydrogen-bonding catalyst-Synthesis of optically active tetrahydro-β-carbolines Org. Biomol. Chem. 2005, 3, 2566-2571
    • (2005) Org. Biomol. Chem. , vol.3 , pp. 2566-2571
    • Zhuang, W.1    Hazell, R.G.2    Jørgensen, K.A.3
  • 44
    • 31144455178 scopus 로고    scopus 로고
    • Asymmetric Friedel-Crafts Alkylations of Indoles with Nitroalkenes Catalyzed by Zn(II)-Bisoxazoline Complexes
    • Jia, Y.-X.; Zhu, S.-F.; Yang, Y.; Zhou, Q.-L. Asymmetric Friedel-Crafts Alkylations of Indoles with Nitroalkenes Catalyzed by Zn(II)-Bisoxazoline Complexes J. Org. Chem. 2006, 71, 75-80
    • (2006) J. Org. Chem. , vol.71 , pp. 75-80
    • Jia, Y.-X.1    Zhu, S.-F.2    Yang, Y.3    Zhou, Q.-L.4
  • 46
    • 33744757023 scopus 로고    scopus 로고
    • Enantioselective Friedel-Crafts Alkylation of Indoles with Nitroalkenes Catalyzed by Bifunctional Tridentate Bis(oxazoline)-Zn(II) Complex
    • Lu, S.-F.; Du, D.-M.; Xu, J. Enantioselective Friedel-Crafts Alkylation of Indoles with Nitroalkenes Catalyzed by Bifunctional Tridentate Bis(oxazoline)-Zn(II) Complex Org. Lett. 2006, 8, 2115-2118
    • (2006) Org. Lett. , vol.8 , pp. 2115-2118
    • Lu, S.-F.1    Du, D.-M.2    Xu, J.3
  • 47
    • 36348935182 scopus 로고    scopus 로고
    • Asymmetric Friedel-Crafts Alkylation of Methoxyfuran with Nitroalkenes Catalyzed by Diphenylamine-Tethered Bis(oxazoline)-Zn(II) Complexes
    • Liu, H.; Xu, J.; Du, D.-M. Asymmetric Friedel-Crafts Alkylation of Methoxyfuran with Nitroalkenes Catalyzed by Diphenylamine-Tethered Bis(oxazoline)-Zn(II) Complexes Org. Lett. 2007, 9, 4725-4728
    • (2007) Org. Lett. , vol.9 , pp. 4725-4728
    • Liu, H.1    Xu, J.2    Du, D.-M.3
  • 49
  • 50
    • 77950243314 scopus 로고    scopus 로고
    • Immobilization of Diphenylamine-Linked Bis(oxazoline) Ligands and Their Application in the Asymmetric Friedel-Crafts Alkylation of Indole Derivatives with Nitroalkenes
    • Liu, H.; Du, D.-M. Immobilization of Diphenylamine-Linked Bis(oxazoline) Ligands and Their Application in the Asymmetric Friedel-Crafts Alkylation of Indole Derivatives with Nitroalkenes Eur. J. Org. Chem. 2010, 2121-2131
    • (2010) Eur. J. Org. Chem. , pp. 2121-2131
    • Liu, H.1    Du, D.-M.2
  • 52
    • 84862290807 scopus 로고    scopus 로고
    • Asymmetric Friedel-Crafts alkylation of indoles with 3-nitro-2 H -chromenes catalyzed by diphenylamine-linked bis(oxazoline) and bis(thiazoline) Zn(II) complexes
    • Jia, Y.; Yang, W.; Du, D.-M. Asymmetric Friedel-Crafts alkylation of indoles with 3-nitro-2 H -chromenes catalyzed by diphenylamine-linked bis(oxazoline) and bis(thiazoline) Zn(II) complexes Org. Biomol. Chem. 2012, 10, 4739-4746
    • (2012) Org. Biomol. Chem. , vol.10 , pp. 4739-4746
    • Jia, Y.1    Yang, W.2    Du, D.-M.3
  • 53
    • 84874281025 scopus 로고    scopus 로고
    • Enantioselective Synthesis of Highly Substituted Chromans by a Zinc(II)-Catalyzed Tandem Friedel-Crafts Alkylation/Michael Addition Reaction
    • Li, C.; Liu, F.-L.; Zou, Y.-Q.; Lu, L.-Q.; Chen, J.-R.; Xiao, W.-J. Enantioselective Synthesis of Highly Substituted Chromans by a Zinc(II)-Catalyzed Tandem Friedel-Crafts Alkylation/Michael Addition Reaction Synthesis 2013, 45, 601-605
    • (2013) Synthesis , vol.45 , pp. 601-605
    • Li, C.1    Liu, F.-L.2    Zou, Y.-Q.3    Lu, L.-Q.4    Chen, J.-R.5    Xiao, W.-J.6
  • 56
    • 58349091443 scopus 로고    scopus 로고
    • Recent advances in enantioselective trifluoromethylation reactions
    • Shibata, N.; Mizuta, S.; Kawai, H. Recent advances in enantioselective trifluoromethylation reactions Tetrahedron: Asymmetry 2008, 19, 2633-2644
    • (2008) Tetrahedron: Asymmetry , vol.19 , pp. 2633-2644
    • Shibata, N.1    Mizuta, S.2    Kawai, H.3
  • 57
    • 79551702999 scopus 로고    scopus 로고
    • Enantioselective Organocatalytic Synthesis of Fluorinated Molecules
    • Valero, G.; Companyo, X.; Rios, R. Enantioselective Organocatalytic Synthesis of Fluorinated Molecules Chem.-Eur. J. 2011, 17, 2018-2037
    • (2011) Chem.-Eur. J. , vol.17 , pp. 2018-2037
    • Valero, G.1    Companyo, X.2    Rios, R.3
  • 58
    • 84860377516 scopus 로고    scopus 로고
    • The New Age of Electrophilic Perfluoroalkylation Reactions
    • Macé, Y.; Magnier, E. The New Age of Electrophilic Perfluoroalkylation Reactions Eur. J. Org. Chem. 2012, 2479-2494
    • (2012) Eur. J. Org. Chem. , pp. 2479-2494
    • Macé, Y.1    Magnier, E.2
  • 60
    • 33644919105 scopus 로고    scopus 로고
    • Novel 10-I-3 Hypervalent Iodine-Based Compounds for Electrophilic Trifluoromethylation
    • Eisenberger, P.; Gischig, S.; Togni, A. Novel 10-I-3 Hypervalent Iodine-Based Compounds for Electrophilic Trifluoromethylation Chem.-Eur. J. 2006, 12, 2579-2586
    • (2006) Chem.-Eur. J. , vol.12 , pp. 2579-2586
    • Eisenberger, P.1    Gischig, S.2    Togni, A.3
  • 62
    • 70349908279 scopus 로고    scopus 로고
    • Catalytic Enantioselective Trifluoromethylation of Azomethine Imines with Trimethyl(trifluoromethyl)silane
    • Kawai, H.; Kusuda, A.; Nakamura, S.; Shiro, M.; Shibata, N. Catalytic Enantioselective Trifluoromethylation of Azomethine Imines with Trimethyl(trifluoromethyl)silane Angew. Chem., Int. Ed. 2009, 48, 6324-6327
    • (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 6324-6327
    • Kawai, H.1    Kusuda, A.2    Nakamura, S.3    Shiro, M.4    Shibata, N.5
  • 63
    • 84863536667 scopus 로고    scopus 로고
    • Highly Enantioselective Copper-Catalyzed Electrophilic Trifluoromethylation of β-Ketoesters
    • Deng, Q.-H.; Wadepohl, H.; Gade, L. H. Highly Enantioselective Copper-Catalyzed Electrophilic Trifluoromethylation of β-Ketoesters J. Am. Chem. Soc. 2012, 134, 10769-10772
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 10769-10772
    • Deng, Q.-H.1    Wadepohl, H.2    Gade, L.H.3
  • 64
    • 8644243613 scopus 로고
    • Partition coefficients and their uses
    • Leo, A.; Hansch, C.; Elkins, D. Partition coefficients and their uses Chem. Rev. 1971, 71, 525-616
    • (1971) Chem. Rev. , vol.71 , pp. 525-616
    • Leo, A.1    Hansch, C.2    Elkins, D.3
  • 67
    • 4243664295 scopus 로고
    • A survey of Hammett substituent constants and resonance and field parameters
    • Hansch, C.; Leo, A.; Taft, R. W. A survey of Hammett substituent constants and resonance and field parameters Chem. Rev. 1991, 91, 165-195
    • (1991) Chem. Rev. , vol.91 , pp. 165-195
    • Hansch, C.1    Leo, A.2    Taft, R.W.3
  • 68
    • 84875189703 scopus 로고    scopus 로고
    • An Electrophilic Hypervalent Iodine Reagent for Trifluoromethylthiolation
    • Shao, X.; Wang, X.; Yang, T.; Lu, L.; Shen, Q. An Electrophilic Hypervalent Iodine Reagent for Trifluoromethylthiolation Angew. Chem., Int. Ed. 2013, 52, 3457-3460
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 3457-3460
    • Shao, X.1    Wang, X.2    Yang, T.3    Lu, L.4    Shen, Q.5
  • 69
    • 84891495010 scopus 로고    scopus 로고
    • Copper-Boxmi Complexes as Highly Enantioselective Catalysts for Electrophilic Trifluoromethylthiolations
    • Deng, Q.-H.; Rettenmeier, C.; Wadepohl, H.; Gade, L. H. Copper-Boxmi Complexes as Highly Enantioselective Catalysts for Electrophilic Trifluoromethylthiolations Chem.-Eur. J. 2014, 20, 93-97
    • (2014) Chem.-Eur. J. , vol.20 , pp. 93-97
    • Deng, Q.-H.1    Rettenmeier, C.2    Wadepohl, H.3    Gade, L.H.4
  • 70
    • 24044531286 scopus 로고    scopus 로고
    • Organic Azides: An Exploding Diversity of a Unique Class of Compounds
    • Bräse, S.; Gil, C.; Knepper, K.; Zimmermann, V. Organic Azides: An Exploding Diversity of a Unique Class of Compounds Angew. Chem., Int. Ed. 2005, 44, 5188-5240
    • (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 5188-5240
    • Bräse, S.1    Gil, C.2    Knepper, K.3    Zimmermann, V.4
  • 72
    • 84876026225 scopus 로고    scopus 로고
    • Enantioselective Iron-Catalyzed Azidation of β-Keto Esters and Oxindoles
    • Deng, Q.-H.; Bleith, T.; Wadepohl, H.; Gade, L. H. Enantioselective Iron-Catalyzed Azidation of β-Keto Esters and Oxindoles J. Am. Chem. Soc. 2013, 135, 5356-5359
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 5356-5359
    • Deng, Q.-H.1    Bleith, T.2    Wadepohl, H.3    Gade, L.H.4
  • 73
    • 84856879427 scopus 로고    scopus 로고
    • Highly Enantioselective Copper-Catalyzed Alkylation of β-Ketoesters and Subsequent Cyclization to Spirolactones/Bi-spirolactones
    • Deng, Q.-H.; Wadepohl, H.; Gade, L. H. Highly Enantioselective Copper-Catalyzed Alkylation of β-Ketoesters and Subsequent Cyclization to Spirolactones/Bi-spirolactones J. Am. Chem. Soc. 2012, 134, 2946-2949
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 2946-2949
    • Deng, Q.-H.1    Wadepohl, H.2    Gade, L.H.3
  • 74
    • 84857752743 scopus 로고    scopus 로고
    • 2/Bis(oxazoline) Complex: An Efficient Approach to Fused Heterocycles with a Quaternary Stereocenter
    • 2/Bis(oxazoline) Complex: An Efficient Approach to Fused Heterocycles with a Quaternary Stereocenter Chem.-Asian J. 2012, 7, 493-497
    • (2012) Chem.-Asian J. , vol.7 , pp. 493-497
    • Tan, F.1    Xiao, C.2    Cheng, H.-G.3    Wu, W.4    Ding, K.-R.5    Xiao, W.-J.6
  • 75
    • 48849112023 scopus 로고    scopus 로고
    • Chiral Bis(pyridylimino)isoindoles: A Highly Modular Class of Pincer Ligands for Enantioselective Catalysis
    • Langlotz, B. K.; Wadepohl, H.; Gade, L. H. Chiral Bis(pyridylimino)isoindoles: A Highly Modular Class of Pincer Ligands for Enantioselective Catalysis Angew. Chem., Int. Ed. 2008, 47, 4670-4674
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 4670-4674
    • Langlotz, B.K.1    Wadepohl, H.2    Gade, L.H.3
  • 76
    • 85027943349 scopus 로고    scopus 로고
    • Chromophores, Fluorophores, and Robust Ancillary Ligands for Molecular Catalysts: 1,3-Bis(2-pyridylimino)isoindolines
    • Sauer, D. C.; Melen, R. L.; Kruck, M.; Gade, L. H. Chromophores, Fluorophores, and Robust Ancillary Ligands for Molecular Catalysts: 1,3-Bis(2-pyridylimino)isoindolines Eur. J. Inorg. Chem. 2014, 10.1002/ejic.201402595
    • (2014) Eur. J. Inorg. Chem.
    • Sauer, D.C.1    Melen, R.L.2    Kruck, M.3    Gade, L.H.4
  • 77
    • 84870526093 scopus 로고    scopus 로고
    • Cobalt Alkyl Complexes of a New Family of Chiral 1,3-Bis(2-pyridylimino)isoindolates and Their Application in Asymmetric Hydrosilylation
    • Sauer, D. C.; Wadepohl, H.; Gade, L. H. Cobalt Alkyl Complexes of a New Family of Chiral 1,3-Bis(2-pyridylimino)isoindolates and Their Application in Asymmetric Hydrosilylation Inorg. Chem. 2012, 51, 12948-12958
    • (2012) Inorg. Chem. , vol.51 , pp. 12948-12958
    • Sauer, D.C.1    Wadepohl, H.2    Gade, L.H.3
  • 78
    • 78650084572 scopus 로고    scopus 로고
    • Asymmetric Iron-Catalyzed Hydrosilane Reduction of Ketones: Effect of Zinc Metal upon the Absolute Configuration
    • Inagaki, T.; Ito, A.; Ito, J.-i.; Nishiyama, H. Asymmetric Iron-Catalyzed Hydrosilane Reduction of Ketones: Effect of Zinc Metal upon the Absolute Configuration Angew. Chem., Int. Ed. 2010, 49, 9384-9387
    • (2010) Angew. Chem., Int. Ed. , vol.49 , pp. 9384-9387
    • Inagaki, T.1    Ito, A.2    Ito, J.-I.3    Nishiyama, H.4
  • 79
    • 77649220413 scopus 로고    scopus 로고
    • Iron- and Cobalt-Catalyzed Asymmetric Hydrosilylation of Ketones and Enones with Bis(oxazolinylphenyl)amine Ligands
    • Inagaki, T.; Phong, L. T.; Furuta, A.; Ito, J.-i.; Nishiyama, H. Iron- and Cobalt-Catalyzed Asymmetric Hydrosilylation of Ketones and Enones with Bis(oxazolinylphenyl)amine Ligands Chem.-Eur. J. 2010, 16, 3090-3096
    • (2010) Chem.-Eur. J. , vol.16 , pp. 3090-3096
    • Inagaki, T.1    Phong, L.T.2    Furuta, A.3    Ito, J.-I.4    Nishiyama, H.5
  • 80
    • 33846927966 scopus 로고    scopus 로고
    • An iron-catalysed hydrosilylation of ketones
    • Nishiyama, H.; Furuta, A. An iron-catalysed hydrosilylation of ketones Chem. Commun. 2007, 760-762
    • (2007) Chem. Commun. , pp. 760-762
    • Nishiyama, H.1    Furuta, A.2
  • 81
    • 49949143547 scopus 로고
    • Asymmetric induction in carbenoid reaction by means of a dissymmetric copper chelate
    • Nozaki, H.; Moriuti, S.; Takaya, H.; Noyori, R. Asymmetric induction in carbenoid reaction by means of a dissymmetric copper chelate Tetrahedron Lett. 1966, 7, 5239-5244
    • (1966) Tetrahedron Lett. , vol.7 , pp. 5239-5244
    • Nozaki, H.1    Moriuti, S.2    Takaya, H.3    Noyori, R.4
  • 83
    • 33745048479 scopus 로고    scopus 로고
    • 2-Symmetric Tridentate Bis(oxazoline) and Bis(thiazoline) Zinc Complexes
    • 2-Symmetric Tridentate Bis(oxazoline) and Bis(thiazoline) Zinc Complexes J. Am. Chem. Soc. 2006, 128, 7418-7419
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 7418-7419
    • Lu, S.-F.1    Du, D.-M.2    Xu, J.3    Zhang, S.-W.4
  • 84
    • 3743082936 scopus 로고
    • Heterocycle formation from 1,3-dinitroalkanes. A novel pyrazole synthesis
    • Escribano, F. C.; Alcántara, M. D.; Gómez-Sánchez, A. Heterocycle formation from 1,3-dinitroalkanes. A novel pyrazole synthesis Tetrahedron Lett. 1988, 29, 6001-6004
    • (1988) Tetrahedron Lett. , vol.29 , pp. 6001-6004
    • Escribano, F.C.1    Alcántara, M.D.2    Gómez-Sánchez, A.3
  • 85
    • 0000307757 scopus 로고
    • A Novel Approach to the Synthesis of 1,3,3-trinitroazetidine
    • references therein
    • Marchand, A. P.; Rajagopal, D.; Bott, S. G.; Archibold, T. G. A Novel Approach to the Synthesis of 1,3,3-trinitroazetidine J. Org. Chem. 1995, 60, 4943-4946 and references therein.
    • (1995) J. Org. Chem. , vol.60 , pp. 4943-4946
    • Marchand, A.P.1    Rajagopal, D.2    Bott, S.G.3    Archibold, T.G.4
  • 86
    • 0000851805 scopus 로고
    • Trost, B. M. Heathcock, C. H. Pergamon: Oxford, U.K
    • Rosini, G. In Comprehensive Organic Synthesis; Trost, B. M.; Heathcock, C. H., Eds.; Pergamon: Oxford, U.K., 1991; Vol. 2, pp 321-340.
    • (1991) Comprehensive Organic Synthesis , vol.2 , pp. 321-340
    • Rosini, G.1
  • 88
    • 0037434136 scopus 로고    scopus 로고
    • Asymmetric Catalytic Aza-Henry Reactions Leading to 1,2-Diamines and 1,2-Diaminocarboxylic Acids
    • Westermann, B. Asymmetric Catalytic Aza-Henry Reactions Leading to 1,2-Diamines and 1,2-Diaminocarboxylic Acids Angew. Chem., Int. Ed. 2003, 42, 151-153
    • (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 151-153
    • Westermann, B.1
  • 89
    • 17744381382 scopus 로고    scopus 로고
    • 2-Symmetric Tridentate Bis(oxazoline) and Bis(thiazoline) Complexes: Metal-Controlled Reversal of Enantioselectivity
    • 2-Symmetric Tridentate Bis(oxazoline) and Bis(thiazoline) Complexes: Metal-Controlled Reversal of Enantioselectivity J. Org. Chem. 2005, 70, 3712-3715
    • (2005) J. Org. Chem. , vol.70 , pp. 3712-3715
    • Du, D.-M.1    Lu, S.-F.2    Fang, T.3    Xu, J.4
  • 90
    • 84905670207 scopus 로고    scopus 로고
    • Stereoselective Hydro-dehalogenation via a Radical Based Mechanism Involving T-Shaped Chiral Nickel(I) Pincer Complexes
    • Rettenmeier, C.; Wadepohl, H.; Gade, L. H. Stereoselective Hydro-dehalogenation via a Radical Based Mechanism Involving T-Shaped Chiral Nickel(I) Pincer Complexes Chem.-Eur. J. 2014, 20, 9657-9665
    • (2014) Chem.-Eur. J. , vol.20 , pp. 9657-9665
    • Rettenmeier, C.1    Wadepohl, H.2    Gade, L.H.3
  • 93
    • 84865439282 scopus 로고    scopus 로고
    • A Non-Heme Iron(III) Complex with Porphyrin-like Properties That Catalyzes Asymmetric Epoxidation
    • Niwa, T.; Nakada, M. A Non-Heme Iron(III) Complex with Porphyrin-like Properties That Catalyzes Asymmetric Epoxidation J. Am. Chem. Soc. 2012, 134, 13538-13541
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 13538-13541
    • Niwa, T.1    Nakada, M.2
  • 94
    • 84868563738 scopus 로고    scopus 로고
    • Calcium amido-bisoxazoline complexes in asymmetric hydroamination/cyclisation catalysis
    • Nixon, T. D.; Ward, B. D. Calcium amido-bisoxazoline complexes in asymmetric hydroamination/cyclisation catalysis Chem. Commun. 2012, 48, 11790-11792
    • (2012) Chem. Commun. , vol.48 , pp. 11790-11792
    • Nixon, T.D.1    Ward, B.D.2
  • 95
    • 84896466528 scopus 로고    scopus 로고
    • Chiral lanthanide complexes: Coordination chemistry, spectroscopy, and catalysis
    • Bennett, S. D.; Core, B. A.; Blake, M. P.; Pope, S. J. A.; Mountford, P.; Ward, B. D. Chiral lanthanide complexes: Coordination chemistry, spectroscopy, and catalysis Dalton Trans. 2014, 43, 5871-5885
    • (2014) Dalton Trans. , vol.43 , pp. 5871-5885
    • Bennett, S.D.1    Core, B.A.2    Blake, M.P.3    Pope, S.J.A.4    Mountford, P.5    Ward, B.D.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.