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Volumn 49, Issue 10, 2016, Pages 2261-2272

Merging Visible Light Photoredox and Gold Catalysis

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EID: 84991784019     PISSN: 00014842     EISSN: 15204898     Source Type: Journal    
DOI: 10.1021/acs.accounts.6b00351     Document Type: Article
Times cited : (532)

References (56)
  • 2
    • 33947578482 scopus 로고    scopus 로고
    • Relativistic effects in homogeneous gold catalysis
    • Gorin, D. J.; Toste, F. D. Relativistic effects in homogeneous gold catalysis Nature 2007, 446, 395-403 10.1038/nature05592
    • (2007) Nature , vol.446 , pp. 395-403
    • Gorin, D.J.1    Toste, F.D.2
  • 3
    • 70350496890 scopus 로고    scopus 로고
    • Gold and platinum catalysis - A convenient tool for generating molecular complexity
    • Fürstner, A. Gold and platinum catalysis-a convenient tool for generating molecular complexity Chem. Soc. Rev. 2009, 38, 3208-3221 10.1039/b816696j
    • (2009) Chem. Soc. Rev. , vol.38 , pp. 3208-3221
    • Fürstner, A.1
  • 4
    • 79952686693 scopus 로고    scopus 로고
    • Gold-Catalyzed Nucleophilic Cyclization of Functionalized Allenes: A Powerful Access to Carbo- and Heterocycles
    • Krause, N.; Winter, C. Gold-Catalyzed Nucleophilic Cyclization of Functionalized Allenes: A Powerful Access to Carbo- and Heterocycles Chem. Rev. 2011, 111, 1994-2009 10.1021/cr1004088
    • (2011) Chem. Rev. , vol.111 , pp. 1994-2009
    • Krause, N.1    Winter, C.2
  • 5
    • 79951861392 scopus 로고    scopus 로고
    • Gold-catalyzed decorations of arenes and heteroarenes with C-C multiple bonds
    • Bandini, M. Gold-catalyzed decorations of arenes and heteroarenes with C-C multiple bonds Chem. Soc. Rev. 2011, 40, 1358-1367 10.1039/C0CS00041H
    • (2011) Chem. Soc. Rev. , vol.40 , pp. 1358-1367
    • Bandini, M.1
  • 6
    • 84935009621 scopus 로고    scopus 로고
    • Gold(I)-Catalyzed Activation of Alkynes for the Construction of Molecular Complexity
    • Dorel, R.; Echavarren, A. M. Gold(I)-Catalyzed Activation of Alkynes for the Construction of Molecular Complexity Chem. Rev. 2015, 115, 9028-9072 10.1021/cr500691k
    • (2015) Chem. Rev. , vol.115 , pp. 9028-9072
    • Dorel, R.1    Echavarren, A.M.2
  • 7
    • 84945310635 scopus 로고
    • Standard Electrode Potentials and Temperature Coefficients in Water at 298.15 K
    • Bratsch, S. G. Standard Electrode Potentials and Temperature Coefficients in Water at 298.15 K J. Phys. Chem. Ref. Data 1989, 18, 1-21 10.1063/1.555839
    • (1989) J. Phys. Chem. Ref. Data , vol.18 , pp. 1-21
    • Bratsch, S.G.1
  • 8
    • 79960298576 scopus 로고    scopus 로고
    • III Catalysis: An Alternative Approach for C-C Oxidative Coupling
    • III Catalysis: An Alternative Approach for C-C Oxidative Coupling Chem.-Eur. J. 2011, 17, 8248-8262 10.1002/chem.201100736
    • (2011) Chem. - Eur. J. , vol.17 , pp. 8248-8262
    • Hopkinson, M.N.1    Gee, A.D.2    Gouverneur, V.3
  • 9
    • 80052088155 scopus 로고    scopus 로고
    • Gold for C-C Coupling Reactions: A Swiss-Army-Knife Catalyst?
    • Wegner, H. A.; Auzias, M. Gold for C-C Coupling Reactions: A Swiss-Army-Knife Catalyst? Angew. Chem., Int. Ed. 2011, 50, 8236-8247 10.1002/anie.201101603
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 8236-8247
    • Wegner, H.A.1    Auzias, M.2
  • 10
    • 37049105998 scopus 로고
    • Reactions of trifluoromethyl iodide with methylgold(I) complexes. Preparation of trifluoromethyl-gold(I) and -gold(III) complexes
    • Johnson, A.; Puddephatt, R. J. Reactions of trifluoromethyl iodide with methylgold(I) complexes. Preparation of trifluoromethyl-gold(I) and -gold(III) complexes J. Chem. Soc., Dalton Trans. 1976, 1360-1363 10.1039/dt9760001360
    • (1976) J. Chem. Soc., Dalton Trans. , pp. 1360-1363
    • Johnson, A.1    Puddephatt, R.J.2
  • 12
    • 33745685969 scopus 로고    scopus 로고
    • Radical Trapping by Gold Chlorides Forming Organogold Intermediates
    • Aprile, C.; Boronat, M.; Ferrer, B.; Corma, A.; García, H. Radical Trapping by Gold Chlorides Forming Organogold Intermediates J. Am. Chem. Soc. 2006, 128, 8388-8389 10.1021/ja062000q
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 8388-8389
    • Aprile, C.1    Boronat, M.2    Ferrer, B.3    Corma, A.4    García, H.5
  • 13
    • 68149126733 scopus 로고    scopus 로고
    • Palladium-Catalyzed Decarboxylative Arylation of C-H Bonds by Aryl Acylperoxides
    • Yu, W.-Y.; Sit, N. G.; Zhou, Z.; Chan, A. S.-C. Palladium-Catalyzed Decarboxylative Arylation of C-H Bonds by Aryl Acylperoxides Org. Lett. 2009, 11, 3174-3177 10.1021/ol900756g
    • (2009) Org. Lett. , vol.11 , pp. 3174-3177
    • Yu, W.-Y.1    Sit, N.G.2    Zhou, Z.3    Chan, A.S.-C.4
  • 14
    • 83055161587 scopus 로고    scopus 로고
    • Room-Temperature C-H Arylation: Merger of Pd-Catalyzed C-H Functionalization and Visible-Light Photocatalysis
    • Kalyani, D.; McMurtrey, K. B.; Neufeldt, S. R.; Sanford, M. S. Room-Temperature C-H Arylation: Merger of Pd-Catalyzed C-H Functionalization and Visible-Light Photocatalysis J. Am. Chem. Soc. 2011, 133, 18566-18569 10.1021/ja208068w
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 18566-18569
    • Kalyani, D.1    McMurtrey, K.B.2    Neufeldt, S.R.3    Sanford, M.S.4
  • 15
    • 78650383080 scopus 로고    scopus 로고
    • Visible light photoredox catalysis: Applications in organic synthesis
    • Narayanam, J. M. R.; Stephenson, C. R. J. Visible light photoredox catalysis: applications in organic synthesis Chem. Soc. Rev. 2011, 40, 102-113 10.1039/B913880N
    • (2011) Chem. Soc. Rev. , vol.40 , pp. 102-113
    • Narayanam, J.M.R.1    Stephenson, C.R.J.2
  • 16
    • 84863643233 scopus 로고    scopus 로고
    • Visible-Light Photoredox Catalysis
    • Xuan, J.; Xiao, W.-J. Visible-Light Photoredox Catalysis Angew. Chem., Int. Ed. 2012, 51, 6828-6838 10.1002/anie.201200223
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 6828-6838
    • Xuan, J.1    Xiao, W.-J.2
  • 17
    • 84880124916 scopus 로고    scopus 로고
    • Visible Light Photoredox Catalysis with Transition Metal Complexes: Applications in Organic Synthesis
    • Prier, C. K.; Rankic, D. A.; MacMillan, D. W. C. Visible Light Photoredox Catalysis with Transition Metal Complexes: Applications in Organic Synthesis Chem. Rev. 2013, 113, 5322-5363 10.1021/cr300503r
    • (2013) Chem. Rev. , vol.113 , pp. 5322-5363
    • Prier, C.K.1    Rankic, D.A.2    MacMillan, D.W.C.3
  • 18
    • 84896707663 scopus 로고    scopus 로고
    • Solar Synthesis: Prospects in Visible Light Photocatalysis
    • Schultz, D. M.; Yoon, T. P. Solar Synthesis: Prospects in Visible Light Photocatalysis Science 2014, 343, 1239176 10.1126/science.1239176
    • (2014) Science , vol.343 , pp. 1239176
    • Schultz, D.M.1    Yoon, T.P.2
  • 19
    • 84897915531 scopus 로고    scopus 로고
    • Dual Catalysis sees the Light: Combining Photoredox with Organo-, Acid and Transition-Metal Catalysis
    • Hopkinson, M. N.; Sahoo, B.; Li, J.-L.; Glorius, F. Dual Catalysis sees the Light: Combining Photoredox with Organo-, Acid and Transition-Metal Catalysis Chem.-Eur. J. 2014, 20, 3874-3886 10.1002/chem.201304823
    • (2014) Chem. - Eur. J. , vol.20 , pp. 3874-3886
    • Hopkinson, M.N.1    Sahoo, B.2    Li, J.-L.3    Glorius, F.4
  • 20
    • 84876580516 scopus 로고    scopus 로고
    • The Photocatalyzed Meerwein Arylation: Classic Reaction of Aryl Diazonium Salts in a New Light
    • Hari, D. P.; König, B. The Photocatalyzed Meerwein Arylation: Classic Reaction of Aryl Diazonium Salts in a New Light Angew. Chem., Int. Ed. 2013, 52, 4734-4743 10.1002/anie.201210276
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 4734-4743
    • Hari, D.P.1    König, B.2
  • 21
    • 76149131690 scopus 로고    scopus 로고
    • Homogeneous Gold-Catalyzed Oxidative Carboheterofunctionalization of Alkenes
    • Zhang, G.; Cui, L.; Wang, Y.; Zhang, L. Homogeneous Gold-Catalyzed Oxidative Carboheterofunctionalization of Alkenes J. Am. Chem. Soc. 2010, 132, 1474-1475 10.1021/ja909555d
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 1474-1475
    • Zhang, G.1    Cui, L.2    Wang, Y.3    Zhang, L.4
  • 22
    • 77955030369 scopus 로고    scopus 로고
    • Gold-Catalyzed Intramolecular Aminoarylation of Alkenes: C-C Bond Formation through Bimolecular Reductive Elimination
    • Brenzovich, W. E., Jr.; Benitez, D.; Lackner, A. D.; Shunatona, H. P.; Tkatchouk, E.; Goddard, W. A., III; Toste, F. D. Gold-Catalyzed Intramolecular Aminoarylation of Alkenes: C-C Bond Formation through Bimolecular Reductive Elimination Angew. Chem., Int. Ed. 2010, 49, 5519-5522 10.1002/anie.201002739
    • (2010) Angew. Chem., Int. Ed. , vol.49 , pp. 5519-5522
    • Brenzovich, Jr.W.E.1    Benitez, D.2    Lackner, A.D.3    Shunatona, H.P.4    Tkatchouk, E.5    Goddard, W.A.6    Toste, F.D.7
  • 23
    • 77954273261 scopus 로고    scopus 로고
    • Gold-Catalyzed Three-Component Coupling: Oxidative Oxyarylation of Alkenes
    • Melhado, A. D.; Brenzovich, W. E., Jr.; Lackner, A. D.; Toste, F. D. Gold-Catalyzed Three-Component Coupling: Oxidative Oxyarylation of Alkenes J. Am. Chem. Soc. 2010, 132, 8885-8887 10.1021/ja1034123
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 8885-8887
    • Melhado, A.D.1    Brenzovich, Jr.W.E.2    Lackner, A.D.3    Toste, F.D.4
  • 24
    • 78049510000 scopus 로고    scopus 로고
    • Arylsilanes: Application to Gold-Catalyzed Oxyarylation of Alkenes
    • Ball, L. T.; Lloyd-Jones, G. C.; Russell, C. A.; Green, M. Arylsilanes: Application to Gold-Catalyzed Oxyarylation of Alkenes Org. Lett. 2010, 12, 4724-4727 10.1021/ol1019162
    • (2010) Org. Lett. , vol.12 , pp. 4724-4727
    • Ball, L.T.1    Lloyd-Jones, G.C.2    Russell, C.A.3    Green, M.4
  • 25
    • 78049494200 scopus 로고    scopus 로고
    • Gold-Catalyzed Oxidative Coupling Reactions with Aryltrimethylsilanes
    • Brenzovich, W. E., Jr.; Brazeau, J.-F.; Toste, F. D. Gold-Catalyzed Oxidative Coupling Reactions with Aryltrimethylsilanes Org. Lett. 2010, 12, 4728-4731 10.1021/ol102194c
    • (2010) Org. Lett. , vol.12 , pp. 4728-4731
    • Brenzovich, Jr.W.E.1    Brazeau, J.-F.2    Toste, F.D.3
  • 26
    • 84876487932 scopus 로고    scopus 로고
    • Combining Gold and Photoredox Catalysis: Visible Light-Mediated Oxy- and Aminoarylation of Alkenes
    • Sahoo, B.; Hopkinson, M. N.; Glorius, F. Combining Gold and Photoredox Catalysis: Visible Light-Mediated Oxy- and Aminoarylation of Alkenes J. Am. Chem. Soc. 2013, 135, 5505-5508 10.1021/ja400311h
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 5505-5508
    • Sahoo, B.1    Hopkinson, M.N.2    Glorius, F.3
  • 27
    • 84957544359 scopus 로고    scopus 로고
    • Mechanism of the Visible Light-Mediated Gold-Catalyzed Oxyarylation Reaction of Alkenes
    • Zhang, Q.; Zhang, Z.-Q.; Fu, Y.; Yu, H.-Z. Mechanism of the Visible Light-Mediated Gold-Catalyzed Oxyarylation Reaction of Alkenes ACS Catal. 2016, 6, 798-808 10.1021/acscatal.5b01971
    • (2016) ACS Catal. , vol.6 , pp. 798-808
    • Zhang, Q.1    Zhang, Z.-Q.2    Fu, Y.3    Yu, H.-Z.4
  • 28
    • 84941055830 scopus 로고    scopus 로고
    • Dual Photoredox and Gold Catalysis: Intermolecular Multicomponent Oxyarylation of Alkenes
    • Hopkinson, M. N.; Sahoo, B.; Glorius, F. Dual Photoredox and Gold Catalysis: Intermolecular Multicomponent Oxyarylation of Alkenes Adv. Synth. Catal. 2014, 356, 2794-2800 10.1002/adsc.201400580
    • (2014) Adv. Synth. Catal. , vol.356 , pp. 2794-2800
    • Hopkinson, M.N.1    Sahoo, B.2    Glorius, F.3
  • 29
    • 84871054395 scopus 로고    scopus 로고
    • Combining Transition Metal Catalysis with Radical Chemistry: Dramatic Acceleration of Palladium-Catalyzed C-H Arylation with Diaryliodonium Salts
    • Neufeldt, S. R.; Sanford, M. S. Combining Transition Metal Catalysis with Radical Chemistry: Dramatic Acceleration of Palladium-Catalyzed C-H Arylation with Diaryliodonium Salts Adv. Synth. Catal. 2012, 354, 3517-3522 10.1002/adsc.201200738
    • (2012) Adv. Synth. Catal. , vol.354 , pp. 3517-3522
    • Neufeldt, S.R.1    Sanford, M.S.2
  • 30
    • 84899500083 scopus 로고    scopus 로고
    • Dual Visible Light Photoredox and Gold-Catalyzed Arylative Ring Expansion
    • Shu, X.-Z.; Zhang, M.; He, Y.; Frei, H.; Toste, F. D. Dual Visible Light Photoredox and Gold-Catalyzed Arylative Ring Expansion J. Am. Chem. Soc. 2014, 136, 5844-5847 10.1021/ja500716j
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 5844-5847
    • Shu, X.-Z.1    Zhang, M.2    He, Y.3    Frei, H.4    Toste, F.D.5
  • 31
    • 84939832830 scopus 로고    scopus 로고
    • Catalytic Cross-Coupling of Vinyl Golds with Diazonium Salts under Photoredox and Thermal Conditions
    • Patil, D. V.; Yun, H.; Shin, S. Catalytic Cross-Coupling of Vinyl Golds with Diazonium Salts under Photoredox and Thermal Conditions Adv. Synth. Catal. 2015, 357, 2622-2628 10.1002/adsc.201500525
    • (2015) Adv. Synth. Catal. , vol.357 , pp. 2622-2628
    • Patil, D.V.1    Yun, H.2    Shin, S.3
  • 32
    • 33947353548 scopus 로고
    • The Chemistry of Organic Gold Compounds. III. Direct Introduction of Gold into the Aromatic Nucleus (Preliminary Communication)
    • Kharasch, M. S.; Isbell, H. S. The Chemistry of Organic Gold Compounds. III. Direct Introduction of Gold into the Aromatic Nucleus (Preliminary Communication) J. Am. Chem. Soc. 1931, 53, 3053-3059 10.1021/ja01359a030
    • (1931) J. Am. Chem. Soc. , vol.53 , pp. 3053-3059
    • Kharasch, M.S.1    Isbell, H.S.2
  • 33
    • 79957569118 scopus 로고    scopus 로고
    • Gold-mediated C-H bond functionalisation
    • Boorman, T. C.; Larrosa, I. Gold-mediated C-H bond functionalisation Chem. Soc. Rev. 2011, 40, 1910-1925 10.1039/C0CS00098A
    • (2011) Chem. Soc. Rev. , vol.40 , pp. 1910-1925
    • Boorman, T.C.1    Larrosa, I.2
  • 34
    • 84951197056 scopus 로고    scopus 로고
    • Dual gold/photoredox-catalyzed C(sp)-H arylation of terminal alkynes with diazonium salts
    • Tlahuext-Aca, A.; Hopkinson, M. N.; Sahoo, B.; Glorius, F. Dual gold/photoredox-catalyzed C(sp)-H arylation of terminal alkynes with diazonium salts Chem. Sci. 2016, 7, 89-93 10.1039/C5SC02583D
    • (2016) Chem. Sci. , vol.7 , pp. 89-93
    • Tlahuext-Aca, A.1    Hopkinson, M.N.2    Sahoo, B.3    Glorius, F.4
  • 36
    • 84921341133 scopus 로고    scopus 로고
    • A dual catalytic strategy for carbon-phosphorus cross-coupling via gold and photoredox catalysis
    • He, Y.; Wu, H.; Toste, F. D. A dual catalytic strategy for carbon-phosphorus cross-coupling via gold and photoredox catalysis Chem. Sci. 2015, 6, 1194-1198 10.1039/C4SC03092C
    • (2015) Chem. Sci. , vol.6 , pp. 1194-1198
    • He, Y.1    Wu, H.2    Toste, F.D.3
  • 37
    • 70349782130 scopus 로고    scopus 로고
    • Gold-Catalyzed Homogeneous Oxidative Cross-Coupling Reactions
    • Zhang, G.; Peng, Y.; Cui, L.; Zhang, L. Gold-Catalyzed Homogeneous Oxidative Cross-Coupling Reactions Angew. Chem., Int. Ed. 2009, 48, 3112-3115 10.1002/anie.200900585
    • (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 3112-3115
    • Zhang, G.1    Peng, Y.2    Cui, L.3    Zhang, L.4
  • 39
    • 84957577878 scopus 로고    scopus 로고
    • Cross-Coupling of Meyer-Schuster Intermediates under Dual Gold-Photoredox Catalysis
    • Um, J.; Yun, H.; Shin, S. Cross-Coupling of Meyer-Schuster Intermediates under Dual Gold-Photoredox Catalysis Org. Lett. 2016, 18, 484-487 10.1021/acs.orglett.5b03531
    • (2016) Org. Lett. , vol.18 , pp. 484-487
    • Um, J.1    Yun, H.2    Shin, S.3
  • 40
    • 84965082718 scopus 로고    scopus 로고
    • Domino Meyer-Schuster/Arylation Reaction of Alkynols or Alkynyl Hydroperoxides with Diazonium Salts Promoted by Visible Light under Dual Gold and Ruthenium Catalysis
    • Alcaide, B.; Almendros, P.; Busto, E.; Luna, A. Domino Meyer-Schuster/Arylation Reaction of Alkynols or Alkynyl Hydroperoxides with Diazonium Salts Promoted by Visible Light under Dual Gold and Ruthenium Catalysis Adv. Synth. Catal. 2016, 358, 1526-1533 10.1002/adsc.201600158
    • (2016) Adv. Synth. Catal. , vol.358 , pp. 1526-1533
    • Alcaide, B.1    Almendros, P.2    Busto, E.3    Luna, A.4
  • 41
    • 77957365029 scopus 로고    scopus 로고
    • Fluorine-Enabled Cationic Gold Catalysis: Functionalized Hydration of Alkynes
    • Wang, W.; Jasinski, J.; Hammond, G. B.; Xu, B. Fluorine-Enabled Cationic Gold Catalysis: Functionalized Hydration of Alkynes Angew. Chem., Int. Ed. 2010, 49, 7247-7252 10.1002/anie.201003593
    • (2010) Angew. Chem., Int. Ed. , vol.49 , pp. 7247-7252
    • Wang, W.1    Jasinski, J.2    Hammond, G.B.3    Xu, B.4
  • 42
    • 84929222900 scopus 로고    scopus 로고
    • Regioselectivity in the Au-catalyzed hydration and hydroalkoxylation of alkynes
    • Goodwin, J. A.; Aponick, A. Regioselectivity in the Au-catalyzed hydration and hydroalkoxylation of alkynes Chem. Commun. 2015, 51, 8730-8741 10.1039/C5CC00120J
    • (2015) Chem. Commun. , vol.51 , pp. 8730-8741
    • Goodwin, J.A.1    Aponick, A.2
  • 43
    • 84955172566 scopus 로고    scopus 로고
    • Catalysis of Radical Reactions: A Radical Chemistry Perspective
    • Studer, A.; Curran, D. P. Catalysis of Radical Reactions: A Radical Chemistry Perspective Angew. Chem., Int. Ed. 2016, 55, 58-102 10.1002/anie.201505090
    • (2016) Angew. Chem., Int. Ed. , vol.55 , pp. 58-102
    • Studer, A.1    Curran, D.P.2
  • 44
    • 84960510911 scopus 로고    scopus 로고
    • Photosensitizer-Free Visible Light-Mediated Gold-Catalyzed 1,2-Difunctionalization of Alkynes
    • Huang, L.; Rudolph, M.; Rominger, F.; Hashmi, A. S. K. Photosensitizer-Free Visible Light-Mediated Gold-Catalyzed 1,2-Difunctionalization of Alkynes Angew. Chem., Int. Ed. 2016, 55, 4808-4813 10.1002/anie.201511487
    • (2016) Angew. Chem., Int. Ed. , vol.55 , pp. 4808-4813
    • Huang, L.1    Rudolph, M.2    Rominger, F.3    Hashmi, A.S.K.4
  • 45
    • 84899868476 scopus 로고    scopus 로고
    • On the mechanism of photocatalytic reactions with eosin y
    • Majek, M.; Filace, F.; von Wangelin, A. J. On the mechanism of photocatalytic reactions with eosin Y Beilstein J. Org. Chem. 2014, 10, 981-989 10.3762/bjoc.10.97
    • (2014) Beilstein J. Org. Chem. , vol.10 , pp. 981-989
    • Majek, M.1    Filace, F.2    Von Wangelin, A.J.3
  • 46
    • 84947866890 scopus 로고    scopus 로고
    • Ligand-Assisted Gold-Catalyzed Cross-Coupling with Aryldiazonium Salts: Redox Gold Catalysis without an External Oxidant
    • For another remarkable gold-catalyzed arylation of terminal alkynes using aryldiazonium salts mediated by an external ligand, see
    • For another remarkable gold-catalyzed arylation of terminal alkynes using aryldiazonium salts mediated by an external ligand, see: Cai, R.; Lu, M.; Aguilera, E. Y.; Xi, Y.; Akhmedov, N. G.; Petersen, J. L.; Chen, H.; Shi, X. Ligand-Assisted Gold-Catalyzed Cross-Coupling with Aryldiazonium Salts: Redox Gold Catalysis without an External Oxidant Angew. Chem., Int. Ed. 2015, 54, 8772-8776 10.1002/anie.201503546
    • (2015) Angew. Chem., Int. Ed. , vol.54 , pp. 8772-8776
    • Cai, R.1    Lu, M.2    Aguilera, E.Y.3    Xi, Y.4    Akhmedov, N.G.5    Petersen, J.L.6    Chen, H.7    Shi, X.8
  • 47
    • 84979912175 scopus 로고    scopus 로고
    • Oxidative addition to gold(I) by photoredox catalysis: Straightforward access to diverse (C,N)-cyclometalated gold(III) complexes
    • Tlahuext-Aca, A.; Hopkinson, M. N.; Daniliuc, C. G.; Glorius, F. Oxidative addition to gold(I) by photoredox catalysis: straightforward access to diverse (C,N)-cyclometalated gold(III) complexes Chem.-Eur. J. 2016, 22, 11587-11592 10.1002/chem.201602649
    • (2016) Chem. - Eur. J. , vol.22 , pp. 11587-11592
    • Tlahuext-Aca, A.1    Hopkinson, M.N.2    Daniliuc, C.G.3    Glorius, F.4
  • 50
    • 84922998686 scopus 로고    scopus 로고
    • Stable gold(III) catalysts by oxidative addition of a carbon-carbon bond
    • Wu, C.-Y.; Horibe, T.; Jacobsen, C. B.; Toste, F. D. Stable gold(III) catalysts by oxidative addition of a carbon-carbon bond Nature 2015, 517, 449-454 10.1038/nature14104
    • (2015) Nature , vol.517 , pp. 449-454
    • Wu, C.-Y.1    Horibe, T.2    Jacobsen, C.B.3    Toste, F.D.4
  • 51
    • 75649103176 scopus 로고    scopus 로고
    • Percent buried volume for phosphine and N-heterocyclic carbene ligands: Steric properties in organometallic chemistry
    • bur values obtained from gold(I) chlorides complexes
    • bur values obtained from gold(I) chlorides complexes: Clavier, H.; Nolan, S. P. Percent buried volume for phosphine and N-heterocyclic carbene ligands: steric properties in organometallic chemistry Chem. Commun. 2010, 46, 841-861 10.1039/b922984a
    • (2010) Chem. Commun. , vol.46 , pp. 841-861
    • Clavier, H.1    Nolan, S.P.2
  • 52
    • 84970956304 scopus 로고    scopus 로고
    • A general access to organogold(III) complexes by oxidative addition of diazonium salts
    • Huang, L.; Rominger, F.; Rudolph, M.; Hashmi, A. S. K. A general access to organogold(III) complexes by oxidative addition of diazonium salts Chem. Commun. 2016, 52, 6435-6438 10.1039/C6CC02199A
    • (2016) Chem. Commun. , vol.52 , pp. 6435-6438
    • Huang, L.1    Rominger, F.2    Rudolph, M.3    Hashmi, A.S.K.4
  • 53
    • 84971422033 scopus 로고    scopus 로고
    • Arenediazonium salts as electrophiles for the oxidative addition of gold(I)
    • Asomoza-Solís, E. O.; Rojas-Ocampo, J.; Toscano, R. A.; Porcel, S. Arenediazonium salts as electrophiles for the oxidative addition of gold(I) Chem. Commun. 2016, 52, 7295-7298 10.1039/C6CC03105F
    • (2016) Chem. Commun. , vol.52 , pp. 7295-7298
    • Asomoza-Solís, E.O.1    Rojas-Ocampo, J.2    Toscano, R.A.3    Porcel, S.4
  • 54
    • 84983348100 scopus 로고    scopus 로고
    • Dual Photoredox/Gold Catalysis Arylative Cyclization of o-Alkynylphenols with Aryldiazonium Salts: A Flexible Synthesis of Benzofurans
    • Xia, Z.; Khaled, O.; Mouries-Mansuy, V.; Ollivier, C.; Fensterbank, L. Dual Photoredox/Gold Catalysis Arylative Cyclization of o-Alkynylphenols with Aryldiazonium Salts: A Flexible Synthesis of Benzofurans J. Org. Chem. 2016, 81, 7182-7190 10.1021/acs.joc.6b01060
    • (2016) J. Org. Chem. , vol.81 , pp. 7182-7190
    • Xia, Z.1    Khaled, O.2    Mouries-Mansuy, V.3    Ollivier, C.4    Fensterbank, L.5
  • 55
    • 84981169912 scopus 로고    scopus 로고
    • Gold-catalysed cross-coupling between aryldiazonium salts and arylboronic acids: Probing the usefulness of photoredox conditions
    • Cornilleau, T.; Hermange, P.; Fouquet, E. Gold-catalysed cross-coupling between aryldiazonium salts and arylboronic acids: probing the usefulness of photoredox conditions Chem. Commun. 2016, 52, 10040-10043 10.1039/C6CC04239B
    • (2016) Chem. Commun. , vol.52 , pp. 10040-10043
    • Cornilleau, T.1    Hermange, P.2    Fouquet, E.3
  • 56
    • 84981294841 scopus 로고    scopus 로고
    • Dual gold photoredox C(sp2)-C(sp2) cross couplings - Development and mechanistic studies
    • Gauchot, V.; Lee, A.-L. Dual gold photoredox C(sp2)-C(sp2) cross couplings-development and mechanistic studies Chem. Commun. 2016, 52, 10163-10166 10.1039/C6CC05078F
    • (2016) Chem. Commun. , vol.52 , pp. 10163-10166
    • Gauchot, V.1    Lee, A.-L.2


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