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Volumn 1, Issue , 2017, Pages

The merger of transition metal and photocatalysis

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EID: 85027180777     PISSN: None     EISSN: 23973358     Source Type: Journal    
DOI: 10.1038/s41570-017-0052     Document Type: Review
Times cited : (1625)

References (183)
  • 1
    • 0036570496 scopus 로고    scopus 로고
    • The Nobel prize in chemistry for 2001
    • Ault, A. The Nobel prize in chemistry for 2001. J. Chem. Educ. 79, 572-577 (2002).
    • (2002) J. Chem. Educ. , vol.79 , pp. 572-577
    • Ault, A.1
  • 2
    • 31644447881 scopus 로고    scopus 로고
    • 2005 Nobel prize in chemistry. Development of the E-olefin metathesis method in organic synthesis
    • Casey, C. P. 2005 Nobel prize in chemistry. Development of the E-olefin metathesis method in organic synthesis. J. Chem. Educ. 83, 192-195 (2006).
    • (2006) J. Chem. Educ. , vol.83 , pp. 192-195
    • Casey, C.P.1
  • 3
    • 84862065162 scopus 로고    scopus 로고
    • Palladium-catalyzed cross-coupling: A historical contextual perspective to the 2010 Nobel prize
    • Johansson Seechurn, C. C. C., Kitching, M. O., Colacot, T. J., Snieckus, V. Palladium-catalyzed cross-coupling: A historical contextual perspective to the 2010 Nobel prize. Angew. Chem. Int. Ed. 51, 5062-5085 (2012).
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 5062-5085
    • Johansson Seechurn, C.C.C.1    Kitching, M.O.2    Colacot, T.J.3    Snieckus, V.4
  • 5
    • 84991696045 scopus 로고    scopus 로고
    • Application of palladium-catalyzed C-N cross-coupling reactions
    • Ruiz-Castillo, P., Buchwald, S. L. Application of palladium-catalyzed C-N cross-coupling reactions. Chem. Rev. 116, 12564-12649 (2016).
    • (2016) Chem. Rev. , vol.116 , pp. 12564-12649
    • Ruiz-Castillo, P.1    Buchwald, S.L.2
  • 6
    • 84930633780 scopus 로고
    • Oxygen-atom transfer from nitrous oxide to a nickelmetallacycle. Synthesis, structure, and reactions of [cyclic] ( 2, 2-bipyridine)Ni(OCH2CH2CH2CH2)
    • Matsunaga, P. T., Hillhouse, G. L., Rheingold, A. L. Oxygen-atom transfer from nitrous oxide to a nickelmetallacycle. Synthesis, structure, and reactions of [cyclic] (2, 2-bipyridine)Ni(OCH2CH2CH2CH2). J. Am. Chem. Soc. 115, 2075-2077 (1993).
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 2075-2077
    • Matsunaga, P.T.1    Hillhouse, G.L.2    Rheingold, A.L.3
  • 7
    • 0000424220 scopus 로고
    • Oxygen-atom transfer from nitrous oxide (N=N=O) to nickel alkyls. Syntheses and reactions of nickel(II) alkoxides
    • Matsunaga, P. T., Mavropoulos, J. C., Hillhouse, G. L. Oxygen-atom transfer from nitrous oxide (N=N=O) to nickel alkyls. Syntheses and reactions of nickel(ii) alkoxides. Polyhedron 14, 175-185 (1995).
    • (1995) Polyhedron , vol.14 , pp. 175-185
    • Matsunaga, P.T.1    Mavropoulos, J.C.2    Hillhouse, G.L.3
  • 8
    • 0030758961 scopus 로고    scopus 로고
    • Carbon-oxygen reductive-elimination from nickel(II) oxametallacycles and factors that control formation of ether, aldehyde, alcohol, or ester products
    • Han, R., Hillhouse, G. L. Carbon-oxygen reductive-elimination from nickel(ii) oxametallacycles and factors that control formation of ether, aldehyde, alcohol, or ester products. J. Am. Chem. Soc. 119, 8135-8136 (1997).
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 8135-8136
    • Han, R.1    Hillhouse, G.L.2
  • 9
    • 84924778325 scopus 로고    scopus 로고
    • Design synthesis and carbon-heteroatom coupling reactions of organometallic nickel(IV) complexes
    • Camasso, N. M., Sanford, M. S. Design, synthesis, and carbon-heteroatom coupling reactions of organometallic nickel(iv) complexes. Science 347, 1218-1220 (2013).
    • (2013) Science , vol.347 , pp. 1218-1220
    • Camasso, N.M.1    Sanford, M.S.2
  • 10
    • 0032492942 scopus 로고    scopus 로고
    • New N and O-arylations with phenylboronic acids and cupric acetate
    • Chan, D., Monaco, K., Wang, R., Winter, M. New N and O-arylations with phenylboronic acids and cupric acetate. Tetrahedron Lett. 39, 2933-2936 (1998).
    • (1998) Tetrahedron Lett. , vol.39 , pp. 2933-2936
    • Chan, D.1    Monaco, K.2    Wang, R.3    Winter, M.4
  • 11
    • 0032492980 scopus 로고    scopus 로고
    • Synthesis of diaryl ethers through the copper-promoted arylation of phenols with arylboronic acids. An expedient synthesis of thyroxine
    • Evans, D., Katz, J., West, T. Synthesis of diaryl ethers through the copper-promoted arylation of phenols with arylboronic acids. An expedient synthesis of thyroxine. Tetrahedron Lett. 39, 2937-2942 (1998).
    • (1998) Tetrahedron Lett. , vol.39 , pp. 2937-2942
    • Evans, D.1    Katz, J.2    West, T.3
  • 12
    • 0032493017 scopus 로고    scopus 로고
    • New aryl/heteroaryl C-N bond cross-coupling reactions via arylboronic acid/cupric acetate arylation
    • Lam, P. et al. New aryl/heteroaryl C-N bond cross-coupling reactions via arylboronic acid/cupric acetate arylation. Tetrahedron Lett. 39, 2941-2944 (1998).
    • (1998) Tetrahedron Lett. , vol.39 , pp. 2941-2944
    • Lam, P.1
  • 13
    • 84887657120 scopus 로고    scopus 로고
    • Cu(OTf) 2-mediated fluorination of aryltrifluoroborates with potassium fluoride
    • Ye, Y., Schimler, S. D., Hanley, P. S., Sanford, M. S. Cu(OTf)2-mediated fluorination of aryltrifluoroborates with potassium fluoride. J. Am. Chem. Soc. 135, 16292-16295 (2013).
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 16292-16295
    • Ye, Y.1    Schimler, S.D.2    Hanley, P.S.3    Sanford, M.S.4
  • 14
    • 77956233002 scopus 로고    scopus 로고
    • Pd(II)-catalyzed hydroxyl-directed C-H activation/C-O cyclization: Expedient construction of dihydrobenzofurans
    • Wang, X., Lu, Y., Dai, H.-X., Yu, J.-Q. Pd(ii)-catalyzed hydroxyl-directed C-H activation/C-O cyclization: Expedient construction of dihydrobenzofurans. J. Am. Chem. Soc. 132, 12203-12205 (2010).
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 12203-12205
    • Wang, X.1    Lu, Y.2    Dai, H.-X.3    Yu, J.-Q.4
  • 15
    • 68249138163 scopus 로고    scopus 로고
    • Pd(II)-catalyzed amination of C-H bonds using single-electron or two-electron oxidants
    • Mei, T.-S., Wang, X., Yu, J.-Q. Pd(ii)-catalyzed amination of C-H bonds using single-electron or two-electron oxidants. J. Am. Chem. Soc. 131, 10806-10807 (2009).
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 10806-10807
    • Mei, T.-S.1    Wang, X.2    Yu, J.-Q.3
  • 16
    • 79851471855 scopus 로고    scopus 로고
    • Bystanding F+ oxidants enable selective reductive elimination from high-valent metal centers in catalysis
    • Engle, K. M., Mei, T.-S., Wang, X., Yu, J.-Q. Bystanding F+ oxidants enable selective reductive elimination from high-valent metal centers in catalysis. Angew. Chem. Int. Ed. 50, 1478-1491 (2011).
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 1478-1491
    • Engle, K.M.1    Mei, T.-S.2    Wang, X.3    Yu, J.-Q.4
  • 17
    • 84859616806 scopus 로고    scopus 로고
    • High-valent organometallic copper and palladium in catalysis
    • Hickman, A. J., Sanford, M. S. High-valent organometallic copper and palladium in catalysis. Nature 484, 177-185 (2012).
    • (2012) Nature , vol.484 , pp. 177-185
    • Hickman, A.J.1    Sanford, M.S.2
  • 18
    • 79952435321 scopus 로고    scopus 로고
    • Catalyst control of site selectivity in the PdII/IV-catalyzed direct arylation of naphthalene
    • Hickman, A. J., Sanford, M. S. Catalyst control of site selectivity in the PdII/IV-catalyzed direct arylation of naphthalene. ACS Catal. 1, 170-174 (2011).
    • (2011) ACS Catal. , vol.1 , pp. 170-174
    • Hickman, A.J.1    Sanford, M.S.2
  • 19
    • 9944242650 scopus 로고    scopus 로고
    • Organometallic photochemistry at the end of its first century
    • Bitterwolf, T. E. Organometallic photochemistry at the end of its first century. J. Organometal. Chem. 689, 3939-3952 (2004).
    • (2004) J. Organometal. Chem. , vol.689 , pp. 3939-3952
    • Bitterwolf, T.E.1
  • 20
    • 33845558157 scopus 로고
    • Artificial photosynthesis: Water cleavage into hydrogen and oxygen by visible light
    • Grätzel, M. Artificial photosynthesis: Water cleavage into hydrogen and oxygen by visible light. Acc. Chem. Res. 14, 376-384 (1981).
    • (1981) Acc. Chem. Res. , vol.14 , pp. 376-384
    • Grätzel, M.1
  • 21
    • 0343148642 scopus 로고
    • Chemical approaches to artificial photosynthesis
    • Meyer, T. J. Chemical approaches to artificial photosynthesis. Acc. Chem. Res. 22, 163-170 (1989).
    • (1989) Acc. Chem. Res. , vol.22 , pp. 163-170
    • Meyer, T.J.1
  • 22
    • 33750558882 scopus 로고    scopus 로고
    • Synthetically tailored excited states: Phosphorescent, cyclometalated iridium(III) complexes and their applications
    • Lowry, M. S., Bernhard, S. Synthetically tailored excited states: Phosphorescent, cyclometalated iridium(iii) complexes and their applications. Chem. Eur. J. 12, 7970-7977 (2006).
    • (2006) Chem. Eur. J. , vol.12 , pp. 7970-7977
    • Lowry, M.S.1    Bernhard, S.2
  • 23
    • 0346980355 scopus 로고    scopus 로고
    • Applications of functionalized transition metal complexes in photonic and optoelectronic devices
    • Kalyanasundaram, K., Grätzel, M. Applications of functionalized transition metal complexes in photonic and optoelectronic devices. Coord. Chem. Rev. 177, 347-414 (1998).
    • (1998) Coord. Chem. Rev. , vol.177 , pp. 347-414
    • Kalyanasundaram, K.1    Grätzel, M.2
  • 24
    • 84983344352 scopus 로고    scopus 로고
    • Photoredox catalysis in organic chemistry
    • Shaw, M. H., Twilton, J., MacMillan, D. W. C. Photoredox catalysis in organic chemistry. J. Org. Chem. 81, 6898-6926 (2016).
    • (2016) J. Org. Chem. , vol.81 , pp. 6898-6926
    • Shaw, M.H.1    Twilton, J.2    MacMillan, D.W.C.3
  • 25
    • 0001450665 scopus 로고
    • Selective catalytic dehydrogenation of alkanes to alkenes
    • Burk, M. J., Crabtree, R. H. Selective catalytic dehydrogenation of alkanes to alkenes. J. Am. Chem. Soc. 109, 8025-8032 (1987).
    • (1987) J. Am. Chem. Soc. , vol.109 , pp. 8025-8032
    • Burk, M.J.1    Crabtree, R.H.2
  • 26
    • 0001562807 scopus 로고
    • Photochemical dehydrogenation of alkanes catalyzed by trans-carbonylchlorobis(trimethylphosphine) rhodium: Aspects of selectivity and mechanism
    • Maguire, J. A., Boese, W. T., Goldman, A. S. Photochemical dehydrogenation of alkanes catalyzed by trans-carbonylchlorobis(trimethylphosphine) rhodium: Aspects of selectivity and mechanism. J. Am. Chem. Soc. 111, 7088-7093 (1989).
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 7088-7093
    • Maguire, J.A.1    Boese, W.T.2    Goldman, A.S.3
  • 27
    • 0000997549 scopus 로고
    • Carbonylation of hydrocarbons via carbon-hydrogen activation catalyzed by RhCl(CO)(PMe3)2 under irradiation
    • Sakakura, T., Sodeyama, T., Sasaki, K., Wada, K., Tanaka, M. Carbonylation of hydrocarbons via carbon-hydrogen activation catalyzed by RhCl(CO)(PMe3)2 under irradiation. J. Am. Chem. Soc. 112, 7221-7229 (1990).
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 7221-7229
    • Sakakura, T.1    Sodeyama, T.2    Sasaki, K.3    Wada, K.4    Tanaka, M.5
  • 28
    • 0026046823 scopus 로고
    • Palladium-catalyzed carbonylative cross-coupling reaction of iodoalkanes with 9-alkyl-9-BBN derivatives A direct and selective synthesis of ketones
    • Ishiyama, T., Miyaura, N., Suzuki, A. Palladium-catalyzed carbonylative cross-coupling reaction of iodoalkanes with 9-alkyl-9-BBN derivatives. A direct and selective synthesis of ketones. Tetrahedron Lett. 47, 6923-6926 (1991).
    • (1991) Tetrahedron Lett. , vol.47 , pp. 6923-6926
    • Ishiyama, T.1    Miyaura, N.2    Suzuki, A.3
  • 29
    • 84868238205 scopus 로고    scopus 로고
    • Photoinduced Ullmann C-N coupling: Demonstrating the viability of a radical pathway
    • Creutz, S. E., Lotito, K. J., Fu, G. C., Peters, J. C. Photoinduced Ullmann C-N coupling: Demonstrating the viability of a radical pathway. Science 338, 647-651 (2012).
    • (2012) Science , vol.338 , pp. 647-651
    • Creutz, S.E.1    Lotito, K.J.2    Fu, G.C.3    Peters, J.C.4
  • 30
    • 0345329013 scopus 로고
    • Copper assisted nucleophilic substitution of aryl halogen
    • Lindsey, J. Copper assisted nucleophilic substitution of aryl halogen. Tetrahedron 40, 1433-1456 (1984).
    • (1984) Tetrahedron , vol.40 , pp. 1433-1456
    • Lindsey, J.1
  • 31
    • 84879350547 scopus 로고    scopus 로고
    • Synthesis of alkyl aryl ketones by Pd/light induced carbonylative cross-coupling of alkyl iodides and arylboronic acids
    • Sumino, S., Ui, T., Ryu, I. Synthesis of alkyl aryl ketones by Pd/light induced carbonylative cross-coupling of alkyl iodides and arylboronic acids. Org. Lett. 15, 3142-3145 (2013).
    • (2013) Org. Lett. , vol.15 , pp. 3142-3145
    • Sumino, S.1    Ui, T.2    Ryu, I.3
  • 32
    • 84957899492 scopus 로고    scopus 로고
    • Asymmetric copper-catalyzed C-N cross-couplings induced by visible light
    • Kainz, Q. M. et al. Asymmetric copper-catalyzed C-N cross-couplings induced by visible light. Science 351, 681-684 (2016).
    • (2016) Science , vol.351 , pp. 681-684
    • Kainz, Q.M.1
  • 33
    • 84987962236 scopus 로고    scopus 로고
    • Photochemical approaches to complex chemotypes: Applications in natural product synthesis
    • Kärkäs, M. D., Porco, J. A. Jr & Stephenson, C. R. J. Photochemical approaches to complex chemotypes: Applications in natural product synthesis. Chem. Rev. 116, 9638-9747 (2016).
    • (2016) Chem. Rev. , vol.116 , pp. 9638-9747
    • Kärkäs, M.D.1    Porco, J.A.2    Stephenson, C.R.J.3
  • 34
    • 79251579273 scopus 로고    scopus 로고
    • Photochemical reactions as key steps in natural product synthesis
    • Bach, T., Hehn, J. P. Photochemical reactions as key steps in natural product synthesis. Angew. Chem. Int. Ed. 50, 1000-1045 (2011).
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 1000-1045
    • Bach, T.1    Hehn, J.P.2
  • 35
    • 42549140767 scopus 로고    scopus 로고
    • Photochemical reactions as key steps in organic synthesis
    • Hoffmann, N. Photochemical reactions as key steps in organic synthesis. Chem. Rev. 108, 1052-1103 (2008).
    • (2008) Chem. Rev. , vol.108 , pp. 1052-1103
    • Hoffmann, N.1
  • 36
    • 84990162781 scopus 로고
    • The beginnings of organic photochemistry
    • Roth, H. D. The beginnings of organic photochemistry. Angew. Chem. Int. Ed. Engl. 28, 1193-1207 (1989).
    • (1989) Angew. Chem. Int. Ed. Engl. , vol.28 , pp. 1193-1207
    • Roth, H.D.1
  • 38
    • 84937193432 scopus 로고
    • Chemische Lichtwirkungen [German]
    • Ciamician, G., Silber, P. Chemische Lichtwirkungen [German]. Ber. Dtsch. Chem. Ges. 41, 1928-1935 (1908).
    • (1908) Ber. Dtsch. Chem. Ges. , vol.41 , pp. 1928-1935
    • Ciamician, G.1    Silber, P.2
  • 39
    • 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. 40, 102-113 (2011).
    • (2011) Chem. Soc. Rev. , vol.40 , pp. 102-113
    • Narayanam, J.M.R.1    Stephenson, C.R.J.2
  • 40
    • 84863643233 scopus 로고    scopus 로고
    • Visible-light photoredox catalysis
    • Xuan, J., Xiao, W.-J. Visible-light photoredox catalysis. Angew. Chem. Int. Ed. 51, 6828-6838 (2012).
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 6828-6838
    • Xuan, J.1    Xiao, W.-J.2
  • 41
    • 84893922336 scopus 로고    scopus 로고
    • Photoredox catalysis for organic syntheses
    • Reckenthäler, M., Griesbeck, A. G. Photoredox catalysis for organic syntheses. Adv. Synth. Catal. 355, 2727-2744 (2013).
    • (2013) Adv. Synth. Catal. , vol.355 , pp. 2727-2744
    • Reckenthäler, M.1    Griesbeck, A.G.2
  • 42
    • 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. 113, 5322-5363 (2013).
    • (2013) Chem. Rev. , vol.113 , pp. 5322-5363
    • Prier, C.K.1    Rankic, D.A.2    MacMillan, D.W.C.3
  • 43
    • 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 343, 1239176 (2014).
    • (2014) Science , vol.343 , pp. 1239176
    • Schultz, D.M.1    Yoon, T.P.2
  • 44
    • 84988014907 scopus 로고    scopus 로고
    • Organic photoredox catalysis
    • Romero, N. A., Nicewicz, D. A. Organic photoredox catalysis. Chem. Rev. 116, 10075-10116 (2016).
    • (2016) Chem. Rev. , vol.116 , pp. 10075-10116
    • Romero, N.A.1    Nicewicz, D.A.2
  • 45
    • 71649103456 scopus 로고    scopus 로고
    • Development of efficient photocatalytic systems for CO2 reduction using mononuclear and multinuclear metal complexes based on mechanistic studies
    • Takeda, H., Ishitani, O. Development of efficient photocatalytic systems for CO2 reduction using mononuclear and multinuclear metal complexes based on mechanistic studies. Coord. Chem. Rev. 254, 346-354 (2010).
    • (2010) Coord. Chem. Rev. , vol.254 , pp. 346-354
    • Takeda, H.1    Ishitani, O.2
  • 46
    • 0001280372 scopus 로고
    • Chemistry of dihydropyridine. 9. Hydride transfer from 1, 4-dihydropyridine to sp3-hybridized carbon in sulfonium salts and activated halides. Studies with NAD(P)H models
    • van Bergen, T. J., Hedstrand, D. M., Kruizinga, W. H., Kellogg, R. M. Chemistry of dihydropyridine. 9. Hydride transfer from 1, 4-dihydropyridine to sp3-hybridized carbon in sulfonium salts and activated halides. Studies with NAD(P)H models. J. Org. Chem. 44, 4953-4962 (1979).
    • (1979) J. Org. Chem. , vol.44 , pp. 4953-4962
    • Van Bergen, T.J.1    Hedstrand, D.M.2    Kruizinga, W.H.3    Kellogg, R.M.4
  • 47
    • 0006891069 scopus 로고
    • Tris(2, 2-bipyridine)ruthenium2+-mediated photoreduction of olefins with 1-benzyl-1, 4-dihydronicotinamide: A mechanistic probe for electron-transfer reactions of NAD(P) H-model compounds
    • Pac, C., Ihama, M., Yasuda, M., Miyauchi, Y., Sakurai, H. Tris(2, 2-bipyridine)ruthenium2+-mediated photoreduction of olefins with 1-benzyl-1, 4-dihydronicotinamide: A mechanistic probe for electron-transfer reactions of NAD(P) H-model compounds. J. Am. Chem. Soc. 103, 6495-6497 (1983).
    • (1983) J. Am. Chem. Soc. , vol.103 , pp. 6495-6497
    • Pac, C.1    Ihama, M.2    Yasuda, M.3    Miyauchi, Y.4    Sakurai, H.5
  • 48
    • 0347852563 scopus 로고
    • Energetic comparison between photoinduced electron-transfer reactions from NADH model compounds to organic and inorganic oxidants and hydride-transfer reactions for NADH model compounds to p-benzoquinone derivatives
    • Fukuzumi, S., Koumitsu, S., Hironaka, K., Tanaka, T. Energetic comparison between photoinduced electron-transfer reactions from NADH model compounds to organic and inorganic oxidants and hydride-transfer reactions for NADH model compounds to p-benzoquinone derivatives. J. Am. Chem. Soc. 109, 305-316 (1987).
    • (1987) J. Am. Chem. Soc. , vol.109 , pp. 305-316
    • Fukuzumi, S.1    Koumitsu, S.2    Hironaka, K.3    Tanaka, T.4
  • 49
    • 0013595380 scopus 로고
    • Photo-oxidation of some carbinols by the Ru(II) polypyridyl complex-aryl diazonium salt system
    • Cano-Yelo, H., Deronzier, A. Photo-oxidation of some carbinols by the Ru(ii) polypyridyl complex-aryl diazonium salt system. Tetrahedron Lett. 25, 5517-5520 (1984).
    • (1984) Tetrahedron Lett. , vol.25 , pp. 5517-5520
    • Cano-Yelo, H.1    Deronzier, A.2
  • 50
    • 0001476677 scopus 로고
    • Photosensitized decarboxylative Michael addition through N-(acyloxy)phthalimides via an electron-transfer mechanism
    • Okada, K., Okamoto, K., Morita, N., Okubo, K., Oda, M. Photosensitized decarboxylative Michael addition through N-(acyloxy)phthalimides via an electron-transfer mechanism. J. Am. Chem. Soc. 113, 9401-9402 (1991).
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 9401-9402
    • Okada, K.1    Okamoto, K.2    Morita, N.3    Okubo, K.4    Oda, M.5
  • 51
    • 53349122064 scopus 로고    scopus 로고
    • Merging photoredox catalysis with organocatalysis: The direct asymmetric alkylation of aldehydes
    • Nicewicz, D. A., MacMillan, D. W. C. Merging photoredox catalysis with organocatalysis: The direct asymmetric alkylation of aldehydes. Science 322, 77-80 (2008).
    • (2008) Science , vol.322 , pp. 77-80
    • Nicewicz, D.A.1    MacMillan, D.W.C.2
  • 52
    • 67650283342 scopus 로고    scopus 로고
    • Efficient visible light photocatalysis of [2+2] enone cycloadditions
    • Ischay, M. A., Anzovino, M. E., Du, J., Yoon, T. P. Efficient visible light photocatalysis of [2+2] enone cycloadditions. J. Am. Chem. Soc. 130, 12886-12887 (2008).
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 12886-12887
    • Ischay, M.A.1    Anzovino, M.E.2    Du, J.3    Yoon, T.P.4
  • 53
    • 67649625293 scopus 로고    scopus 로고
    • Electron-transfer phtotoredox catalysis: Development of a tin-free reductive dehalogenation reaction
    • Narayanam, J. M. R., Tucker, J. W., Stephenson, C. R. J. Electron-transfer phtotoredox catalysis: Development of a tin-free reductive dehalogenation reaction. J. Am. Chem. Soc. 131, 8756-8757 (2009).
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 8756-8757
    • Narayanam, J.M.R.1    Tucker, J.W.2    Stephenson, C.R.J.3
  • 54
    • 84993983004 scopus 로고    scopus 로고
    • The photophysics of photoredox catalysis: A roadmap for catalyst design
    • Arias-Rotondo, D. M., McCusker, J. M. The photophysics of photoredox catalysis: A roadmap for catalyst design. Chem. Soc. Rev. 45, 5803-5820 (2016).
    • (2016) Chem. Soc. Rev. , vol.45 , pp. 5803-5820
    • Arias-Rotondo, D.M.1    McCusker, J.M.2
  • 55
    • 84941652119 scopus 로고    scopus 로고
    • Characterizing chain processes in visible light photoredox catalysis
    • Cismesia, M. A., Yoon, T. P. Characterizing chain processes in visible light photoredox catalysis. Chem. Sci. 6, 5426-5434 (2015).
    • (2015) Chem. Sci. , vol.6 , pp. 5426-5434
    • Cismesia, M.A.1    Yoon, T.P.2
  • 56
    • 84979578174 scopus 로고    scopus 로고
    • Dual catalysis strategies in photochemical synthesis
    • Skubi, K. L., Blum, T. R., Yoon, T. P. Dual catalysis strategies in photochemical synthesis. Chem. Rev. 116, 10035-10074 (2016).
    • (2016) Chem. Rev. , vol.116 , pp. 10035-10074
    • Skubi, K.L.1    Blum, T.R.2    Yoon, T.P.3
  • 57
    • 84897915531 scopus 로고    scopus 로고
    • Dual catalysis see the light: Combining photoredox with organo-, acid, and transition-metal catalysis
    • Hopkinson, M. N., Sahoo, B., Li, J.-L., Glorius, F. Dual catalysis see the light: Combining photoredox with organo-, acid, and transition-metal catalysis. Chem. Eur. J. 20, 3874-3886 (2014).
    • (2014) Chem. Eur. J. , vol.20 , pp. 3874-3886
    • Hopkinson, M.N.1    Sahoo, B.2    Li, J.-L.3    Glorius, F.4
  • 58
    • 85027947989 scopus 로고    scopus 로고
    • Merging visible-light-photoredox and nickel catalysis
    • Vila, C. Merging visible-light-photoredox and nickel catalysis. ChemCatChem 7, 1790-1793 (2015).
    • (2015) ChemCatChem , vol.7 , pp. 1790-1793
    • Vila, C.1
  • 59
    • 84988555163 scopus 로고    scopus 로고
    • Photoredox catalysis unlocks single-electron elementary steps in transition metal catalyzed cross-coupling
    • Levin, M. D., Kim, S., Toste, F. D. Photoredox catalysis unlocks single-electron elementary steps in transition metal catalyzed cross-coupling. ACS Cent. Sci. 2, 293-301 (2016).
    • (2016) ACS Cent. Sci. , vol.2 , pp. 293-301
    • Levin, M.D.1    Kim, S.2    Toste, F.D.3
  • 61
    • 84900544451 scopus 로고    scopus 로고
    • Recent advances in homogeneous nickel catalysis
    • Tasker, S. Z., Standley, E. A., Jamison, T. F. Recent advances in homogeneous nickel catalysis. Nature 509, 299-309 (2014).
    • (2014) Nature , vol.509 , pp. 299-309
    • Tasker, S.Z.1    Standley, E.A.2    Jamison, T.F.3
  • 62
    • 81355154663 scopus 로고    scopus 로고
    • Nickel-catalyzed cross coupling of non-activated alkyl halides: A mechanistic perspective
    • Hu, X. Nickel-catalyzed cross coupling of non-activated alkyl halides: A mechanistic perspective. Chem. Sci. 2, 1867-1886 (2011).
    • (2011) Chem. Sci. , vol.2 , pp. 1867-1886
    • Hu, X.1
  • 63
    • 84898006720 scopus 로고    scopus 로고
    • Decarboxylative arylation of-amino acids via photoredox catalysis: A one-step conversion of biomass to drug pharmacophore
    • Zuo, Z., MacMillan, D. W. C. Decarboxylative arylation of-amino acids via photoredox catalysis: A one-step conversion of biomass to drug pharmacophore. J. Am. Chem. Soc. 136, 5257-5260 (2014).
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 5257-5260
    • Zuo, Z.1    MacMillan, D.W.C.2
  • 64
    • 84905674432 scopus 로고    scopus 로고
    • Carboxylic acids as a traceless activation group for conjugate additions: A three-step synthesis of (±)-Lyrica
    • Chu, L., Ohta, C., Zuo, Z., MacMillan, D. W. C. Carboxylic acids as a traceless activation group for conjugate additions: A three-step synthesis of (±)-Lyrica. J. Am. Chem. Soc. 136, 10886-10889 (2014).
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 10886-10889
    • Chu, L.1    Ohta, C.2    Zuo, Z.3    MacMillan, D.W.C.4
  • 65
    • 84906334075 scopus 로고    scopus 로고
    • Photoredox-vinylation of-amino acids and N-aryl amines
    • Noble, A., MacMillan, D. W. C. Photoredox-vinylation of-amino acids and N-aryl amines. J. Am. Chem. Soc. 136, 11602-11605 (2014).
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 11602-11605
    • Noble, A.1    MacMillan, D.W.C.2
  • 66
    • 84904797499 scopus 로고    scopus 로고
    • Merging photoredox with nickel catalysis: Coupling of-carboxyl sp3-carbons with aryl halides
    • Zuo, Z., Ahneman, D. T., Chu, L., Terrett, J. A., MacMillan, D. W. C. Merging photoredox with nickel catalysis: Coupling of-carboxyl sp3-carbons with aryl halides. Science 345, 437-440 (2014).
    • (2014) Science , vol.345 , pp. 437-440
    • Zuo, Z.1    Ahneman, D.T.2    Chu, L.3    Terrett, J.A.4    MacMillan, D.W.C.5
  • 67
    • 84959018638 scopus 로고    scopus 로고
    • Enantioselective decarboxylative arylation of-amino acids via the merger of photoredox and nickel catalysis
    • Zuo, Z. et al. Enantioselective decarboxylative arylation of-amino acids via the merger of photoredox and nickel catalysis. J. Am. Chem. Soc. 138, 1832-1835 (2015).
    • (2015) J. Am. Chem. Soc. , vol.138 , pp. 1832-1835
    • Zuo, Z.1
  • 68
    • 84921483701 scopus 로고    scopus 로고
    • Merging photoredox and nickel catalysis: Decarboxylative cross-coupling of carboxylic acids with vinyl halides
    • Noble, A., McCarver, S. J., MacMillan, D. W. C. Merging photoredox and nickel catalysis: Decarboxylative cross-coupling of carboxylic acids with vinyl halides. J. Am. Chem. Soc. 137, 624-627 (2015).
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 624-627
    • Noble, A.1    McCarver, S.J.2    MacMillan, D.W.C.3
  • 69
    • 84982303783 scopus 로고    scopus 로고
    • Metallaphotoredox-catalysed sp3-sp3 cross-coupling of carboxylic acids with alkyl halides
    • Johnston, C. P., Smith, R. T., Allmendinger, S., MacMillan, D. W. C. Metallaphotoredox-catalysed sp3-sp3 cross-coupling of carboxylic acids with alkyl halides. Nature 536, 322-325 (2016).
    • (2016) Nature , vol.536 , pp. 322-325
    • Johnston, C.P.1    Smith, R.T.2    Allmendinger, S.3    MacMillan, D.W.C.4
  • 70
    • 79952656192 scopus 로고    scopus 로고
    • Advances in transition metal (Pd, Ni, Fe)-catalyzed cross-coupling reactions using alkyl-organometallics as reaction partners
    • Jana, R., Pathak, T. P., Sigman, M. S. Advances in transition metal (Pd, Ni, Fe)-catalyzed cross-coupling reactions using alkyl-organometallics as reaction partners. Chem. Rev. 111, 1417-1492 (2011).
    • (2011) Chem. Rev. , vol.111 , pp. 1417-1492
    • Jana, R.1    Pathak, T.P.2    Sigman, M.S.3
  • 71
    • 84930268175 scopus 로고    scopus 로고
    • Merging photoredox and nickel catalysis: The direct synthesis of ketones by the decarboxylative arylation of-oxo acids
    • Chu, L., Lipshultz, J. M., MacMillan, D. W. C. Merging photoredox and nickel catalysis: The direct synthesis of ketones by the decarboxylative arylation of-oxo acids. Angew. Chem. Int. Ed. 54, 7929-7933 (2015).
    • (2015) Angew. Chem. Int. Ed. , vol.54 , pp. 7929-7933
    • Chu, L.1    Lipshultz, J.M.2    MacMillan, D.W.C.3
  • 72
    • 84942543591 scopus 로고    scopus 로고
    • Fragment couplings via CO2 extrusion-recombination: Expansion of a classic bond-forming strategy via metallaphotoredox
    • Le, C. C., MacMillan, D. W. C. Fragment couplings via CO2 extrusion-recombination: Expansion of a classic bond-forming strategy via metallaphotoredox. J. Am. Chem. Soc. 137, 11938-11941 (2015).
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 11938-11941
    • Le, C.C.1    MacMillan, D.W.C.2
  • 73
    • 0006425658 scopus 로고
    • Palladium-catalyzed rearrangement of allylic esters of acetoacetic acid to give-unsaturated methyl ketones
    • Shimizu, I., Yamada, T., Tsuji, J. Palladium-catalyzed rearrangement of allylic esters of acetoacetic acid to give ,-unsaturated methyl ketones. Tetrahedron Lett. 21, 3199-3202 (1980).
    • (1980) Tetrahedron Lett. , vol.21 , pp. 3199-3202
    • Shimizu, I.1    Yamada, T.2    Tsuji, J.3
  • 74
    • 0000695867 scopus 로고
    • Facile generation of a reactive palladium(II) enolate intermediate by the decarboxylation of palladium(II)-ketocarboxylate and its utilization in allylic acylation
    • Tsuda, T., Chujo, Y., Nishi, S., Tawara, K., Saegusa, T. Facile generation of a reactive palladium(ii) enolate intermediate by the decarboxylation of palladium(ii)-ketocarboxylate and its utilization in allylic acylation. J. Am. Chem. Soc. 102, 6381-6384 (1980).
    • (1980) J. Am. Chem. Soc. , vol.102 , pp. 6381-6384
    • Tsuda, T.1    Chujo, Y.2    Nishi, S.3    Tawara, K.4    Saegusa, T.5
  • 75
    • 84941249106 scopus 로고    scopus 로고
    • Oxalates as activating groups for alcohols in visible light photoredox catalysis: Formation of quaternary centers by redox-neutral fragment coupling
    • Nawrat, C. C., Jamison, C. R., Slutskyy, Y., MacMillan, D. W. C., Overman, L. E. Oxalates as activating groups for alcohols in visible light photoredox catalysis: Formation of quaternary centers by redox-neutral fragment coupling. J. Am. Chem. Soc. 137, 11270-11273 (2015).
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 11270-11273
    • Nawrat, C.C.1    Jamison, C.R.2    Slutskyy, Y.3    MacMillan, D.W.C.4    Overman, L.E.5
  • 76
    • 84992743753 scopus 로고    scopus 로고
    • Alcohols as latent coupling fragments for metallaphotoredox catalysis: Sp3-sp2 cross-coupling of oxalates with aryl halides
    • Zhang, X., MacMillan, D. W. C. Alcohols as latent coupling fragments for metallaphotoredox catalysis: Sp3-sp2 cross-coupling of oxalates with aryl halides. J. Am. Chem. Soc. 138, 13862-13865 (2016).
    • (2016) J. Am. Chem. Soc. , vol.138 , pp. 13862-13865
    • Zhang, X.1    MacMillan, D.W.C.2
  • 77
    • 84904800842 scopus 로고    scopus 로고
    • Single-electron transmetalation in organoboron cross-coupling by photoredox/nickel dual catalysis
    • Tellis, J. C., Primer, D. N., Molander, G. A. Single-electron transmetalation in organoboron cross-coupling by photoredox/nickel dual catalysis. Science 345, 433-436 (2014).
    • (2014) Science , vol.345 , pp. 433-436
    • Tellis, J.C.1    Primer, D.N.2    Molander, G.A.3
  • 78
    • 84955181954 scopus 로고    scopus 로고
    • Arylation/heteroarylation of chiral-aminomethyltrifluoroborates by synergistic iridium photoredox/nickel cross-coupling catalysis
    • El Khatib, M., Serafim, R. A. M., Molander, G. A.-Arylation/heteroarylation of chiral-aminomethyltrifluoroborates by synergistic iridium photoredox/nickel cross-coupling catalysis. Angew. Chem. Int. Ed. 55, 254-258 (2016).
    • (2016) Angew. Chem. Int. Ed. , vol.55 , pp. 254-258
    • El Khatib, M.1    Serafim, R.A.M.2    Molander, G.A.3
  • 79
    • 84935125121 scopus 로고    scopus 로고
    • Photoredox cross-coupling: Ir/Ni dual catalysis for the synthesis of benzylic ethers
    • Karakaya, I., Primer, D. N., Molander, G. A. Photoredox cross-coupling: Ir/Ni dual catalysis for the synthesis of benzylic ethers. Org. Lett. 17, 3294-3297 (2015).
    • (2015) Org. Lett. , vol.17 , pp. 3294-3297
    • Karakaya, I.1    Primer, D.N.2    Molander, G.A.3
  • 80
    • 84923260920 scopus 로고    scopus 로고
    • Single-electron transmetalation: An enabling technology for secondary alkylboron cross-coupling
    • Primer, D. N., Karakaya, I., Tellis, J. C., Molander, G. A. Single-electron transmetalation: An enabling technology for secondary alkylboron cross-coupling. J. Am. Chem. Soc. 137, 2195-2198 (2015).
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 2195-2198
    • Primer, D.N.1    Karakaya, I.2    Tellis, J.C.3    Molander, G.A.4
  • 81
    • 84959020578 scopus 로고    scopus 로고
    • Visible light photoredox cross-coupling of acyl chlorides with potassium alkoxymethyltrifluoroborates: Synthesis of-alkoxyketones
    • Amani, J., Sodagar, E., Molander, G. A. Visible light photoredox cross-coupling of acyl chlorides with potassium alkoxymethyltrifluoroborates: Synthesis of-alkoxyketones. Org. Lett. 18, 732-735 (2016).
    • (2016) Org. Lett. , vol.18 , pp. 732-735
    • Amani, J.1    Sodagar, E.2    Molander, G.A.3
  • 82
    • 84957577168 scopus 로고    scopus 로고
    • Donor-acceptor fluorophores for visible-light-promoted organic synthesis: Photoredox/Ni dual catalytic C(sp3)-C(sp2) cross-coupling
    • Luo, J., Zhang, J. Donor-acceptor fluorophores for visible-light-promoted organic synthesis: Photoredox/Ni dual catalytic C(sp3)-C(sp2) cross-coupling. ACS Catal. 6, 873-877 (2016).
    • (2016) ACS Catal. , vol.6 , pp. 873-877
    • Luo, J.1    Zhang, J.2
  • 83
    • 84871027786 scopus 로고    scopus 로고
    • Highly efficient organic light-emitting diodes from delayed fluorescence
    • Uoyama, H., Goushi, K., Shizu, K., Nomura, H., Adachi, C. Highly efficient organic light-emitting diodes from delayed fluorescence. Nature 492, 234-238 (2012).
    • (2012) Nature , vol.492 , pp. 234-238
    • Uoyama, H.1    Goushi, K.2    Shizu, K.3    Nomura, H.4    Adachi, C.5
  • 84
    • 84943457879 scopus 로고    scopus 로고
    • Silicates as latent alkyl radical precursors: Visible-light photocatalytic oxidation of hypervalent bis-catecholato silicon compounds
    • Corce, V. et al. Silicates as latent alkyl radical precursors: Visible-light photocatalytic oxidation of hypervalent bis-catecholato silicon compounds. Angew. Chem. Int. Ed. 54, 11414-11418 (2015).
    • (2015) Angew. Chem. Int. Ed. , vol.54 , pp. 11414-11418
    • Corce, V.1
  • 85
    • 84955312797 scopus 로고    scopus 로고
    • Base-free photoredox/nickel dual-catalytic cross-coupling of ammonium alkylsilicates
    • Jouffroy, M., Primer, D. N., Molander, G. A. Base-free photoredox/nickel dual-catalytic cross-coupling of ammonium alkylsilicates. J. Am. Chem. Soc. 138, 475-478 (2016).
    • (2016) J. Am. Chem. Soc. , vol.138 , pp. 475-478
    • Jouffroy, M.1    Primer, D.N.2    Molander, G.A.3
  • 86
    • 84959018709 scopus 로고    scopus 로고
    • Engaging alkenyl halides with alkylsilicates via photoredox dual catalysis
    • Patel, N. R., Kelly, C. B., Jouffroy, M., Molander, G. A. Engaging alkenyl halides with alkylsilicates via photoredox dual catalysis. Org. Lett. 18, 764-767 (2016).
    • (2016) Org. Lett. , vol.18 , pp. 764-767
    • Patel, N.R.1    Kelly, C.B.2    Jouffroy, M.3    Molander, G.A.4
  • 87
    • 85027951578 scopus 로고    scopus 로고
    • Visible-light-mediated aromatic substitution reactions of cyanoarenes with 4-alkyl-1, 4-dihydropyridines through double carbon-carbon bond cleavage
    • Nakajima, K., Nojima, S., Sakata, K., Nishibayashi, Y. Visible-light-mediated aromatic substitution reactions of cyanoarenes with 4-alkyl-1, 4-dihydropyridines through double carbon-carbon bond cleavage. ChemCatChem 8, 1028-1032 (2016).
    • (2016) ChemCatChem , vol.8 , pp. 1028-1032
    • Nakajima, K.1    Nojima, S.2    Sakata, K.3    Nishibayashi, Y.4
  • 88
    • 84857592302 scopus 로고    scopus 로고
    • Transfer hydrogenation with Hantzch esters and related organic hydride donors
    • Zheng, C., You, S.-L. Transfer hydrogenation with Hantzch esters and related organic hydride donors. Chem. Soc. Rev. 41, 2498-2518 (2012).
    • (2012) Chem. Soc. Rev. , vol.41 , pp. 2498-2518
    • Zheng, C.1    You, S.-L.2
  • 89
    • 84992456247 scopus 로고    scopus 로고
    • Nickel-and photoredox-catalyzed cross-coupling reactions of aryl halides with 4-alkyl-1, 4-dihydropyridines as formal nucleophilic alkylation reagents
    • Nakajima, K., Nojima, S., Nishibayashi, Y. Nickel-and photoredox-catalyzed cross-coupling reactions of aryl halides with 4-alkyl-1, 4-dihydropyridines as formal nucleophilic alkylation reagents. Angew. Chem. Int. Ed. 55, 14106-14110 (2016).
    • (2016) Angew. Chem. Int. Ed. , vol.55 , pp. 14106-14110
    • Nakajima, K.1    Nojima, S.2    Nishibayashi, Y.3
  • 90
    • 85046802971 scopus 로고    scopus 로고
    • 1, 4-Dihydropyridines as alkyl radical precursors: Introducing the aldehyde feedstock to nickel/photoredox dual catalysis
    • Gutiérrez-Bonet, Á., Tellis, J. C., Matsui, J. K., Vara, B. A., Molander, G. A. 1, 4-Dihydropyridines as alkyl radical precursors: Introducing the aldehyde feedstock to nickel/photoredox dual catalysis. ACS Catal. 6, 8004-8008 (2016).
    • (2016) ACS Catal. , vol.6 , pp. 8004-8008
    • Gutiérrez-Bonet, Á.1    Tellis, J.C.2    Matsui, J.K.3    Vara, B.A.4    Molander, G.A.5
  • 91
    • 84928492420 scopus 로고    scopus 로고
    • Nickel-catalyzed cross-coupling of photoredox-generated radicals: Uncovering a general manifold for stereoconvergence in nickel-catalyzed cross-couplings
    • Gutierrez, O., Tellis, J. C., Primer, D. N., Molander, G. A., Kozlowski, M. C. Nickel-catalyzed cross-coupling of photoredox-generated radicals: Uncovering a general manifold for stereoconvergence in nickel-catalyzed cross-couplings. J. Am. Chem. Soc. 137, 4896-4899 (2015).
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 4896-4899
    • Gutierrez, O.1    Tellis, J.C.2    Primer, D.N.3    Molander, G.A.4    Kozlowski, M.C.5
  • 92
    • 84995666102 scopus 로고    scopus 로고
    • C-H functionalization of amines with aryl halides by nickel-photoredox catalysis
    • Ahneman, D. T., Doyle, A. G. C-H functionalization of amines with aryl halides by nickel-photoredox catalysis. Chem. Sci. 7, 7002-7006 (2016).
    • (2016) Chem. Sci. , vol.7 , pp. 7002-7006
    • Ahneman, D.T.1    Doyle, A.G.2
  • 93
    • 84942354069 scopus 로고    scopus 로고
    • O-H hydrogen bonding promotes H-atom transfer from-C-H bonds for C-alkylation of alcohols
    • Jeffrey, J. L., Terrett, J. A., MacMillan, D. W. C. O-H hydrogen bonding promotes H-atom transfer from-C-H bonds for C-alkylation of alcohols. Science 349, 1532-1536 (2015).
    • (2015) Science , vol.349 , pp. 1532-1536
    • Jeffrey, J.L.1    Terrett, J.A.2    MacMillan, D.W.C.3
  • 94
    • 84965013481 scopus 로고    scopus 로고
    • Native functionality in triple catalytic cross-coupling: Sp3 C-H bonds as latent nucleophiles
    • Shaw, M. H., Shurtleff, V. W., Terrett, J. A., Cuthbertson, J. D., MacMillan, D. W. C. Native functionality in triple catalytic cross-coupling: Sp3 C-H bonds as latent nucleophiles. Science 352, 1304-1308 (2016).
    • (2016) Science , vol.352 , pp. 1304-1308
    • Shaw, M.H.1    Shurtleff, V.W.2    Terrett, J.A.3    Cuthbertson, J.D.4    MacMillan, D.W.C.5
  • 95
    • 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. 28, 25-35 (1999).
    • (1999) Chem. Soc. Rev. , vol.28 , pp. 25-35
    • Roberts, B.P.1
  • 96
    • 84990046457 scopus 로고    scopus 로고
    • Direct C(sp3)-H cross coupling enabled by catalytic generation of chlorine radicals
    • Shields, B. J., Doyle, A. G. Direct C(sp3)-H cross coupling enabled by catalytic generation of chlorine radicals. J. Am. Chem. Soc. 138, 12719-12722 (2016).
    • (2016) J. Am. Chem. Soc. , vol.138 , pp. 12719-12722
    • Shields, B.J.1    Doyle, A.G.2
  • 97
    • 84944339567 scopus 로고    scopus 로고
    • Halogen photoelimination from monomeric nickel(III) complexes enabled by the secondary coordination sphere
    • Hwang, S. J. et al. Halogen photoelimination from monomeric nickel(iii) complexes enabled by the secondary coordination sphere. Organometallics 34, 4766-4774 (2015).
    • (2015) Organometallics , vol.34 , pp. 4766-4774
    • Hwang, S.J.1
  • 98
    • 84921657427 scopus 로고    scopus 로고
    • Tandem redox mediator/Ni(II) trihalide complex photocycle for hydrogen evolution from HCl
    • Hwang, S. J., Powers, D. C., Maher, A. G., Nocera, D. G. Tandem redox mediator/Ni(ii) trihalide complex photocycle for hydrogen evolution from HCl. Chem. Sci. 6, 917-922 (2015).
    • (2015) Chem. Sci. , vol.6 , pp. 917-922
    • Hwang, S.J.1    Powers, D.C.2    Maher, A.G.3    Nocera, D.G.4
  • 99
    • 84930226057 scopus 로고    scopus 로고
    • Trap-free halogen photoelimination from mononuclear Ni(III) complexes
    • Hwang, S.-J. et al. Trap-free halogen photoelimination from mononuclear Ni(iii) complexes. J. Am. Chem. Soc. 137, 6472-6475 (2015).
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 6472-6475
    • Hwang, S.-J.1
  • 100
    • 84990060414 scopus 로고    scopus 로고
    • Photochemical nickel-catalyzed C-H arylation: Synthetic scope and mechanistic investigations
    • Heitz, D. R., Tellis, J. C., Molander, G. A. Photochemical nickel-catalyzed C-H arylation: Synthetic scope and mechanistic investigations. J. Am. Chem. Soc. 138, 12715-12718 (2016).
    • (2016) J. Am. Chem. Soc. , vol.138 , pp. 12715-12718
    • Heitz, D.R.1    Tellis, J.C.2    Molander, G.A.3
  • 101
    • 84978932764 scopus 로고    scopus 로고
    • Silyl radical activation of alkyl halides in metallaphotoredox catalysis: A unique pathway for cross-electrophile coupling
    • Zhang, P., Le, C. C., MacMillan, D. W. C. Silyl radical activation of alkyl halides in metallaphotoredox catalysis: A unique pathway for cross-electrophile coupling. J. Am. Chem. Soc. 138, 8084-8087 (2016).
    • (2016) J. Am. Chem. Soc. , vol.138 , pp. 8084-8087
    • Zhang, P.1    Le, C.C.2    MacMillan, D.W.C.3
  • 102
    • 0035980304 scopus 로고    scopus 로고
    • An efficient intermolecular palladium-catalyzed synthesis of aryl ethers
    • Torraca, K. E., Huang, X., Parrish, C. A., Buchwald, S. L. An efficient intermolecular palladium-catalyzed synthesis of aryl ethers. J. Am. Chem. Soc. 123, 10770-10771 (2001).
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 10770-10771
    • Torraca, K.E.1    Huang, X.2    Parrish, C.A.3    Buchwald, S.L.4
  • 103
    • 0037047555 scopus 로고    scopus 로고
    • Air stable, sterically hindered ferrocenyl dialkylphosphines for palladium-catalyzed C-C, C-N, and C-O bond forming cross-couplings
    • Kataoka, N., Shelby, Q., Stambuli, J. P., Hartwig, J. F. Air stable, sterically hindered ferrocenyl dialkylphosphines for palladium-catalyzed C-C, C-N, and C-O bond forming cross-couplings. J. Org. Chem. 67, 5553-5566 (2002).
    • (2002) J. Org. Chem. , vol.67 , pp. 5553-5566
    • Kataoka, N.1    Shelby, Q.2    Stambuli, J.P.3    Hartwig, J.F.4
  • 104
    • 0037149634 scopus 로고    scopus 로고
    • Copper-catalyzed coupling of aryl iodides with aliphatic alcohols
    • Wolter, M., Nordmann, G., Job, G. E., Buchwald, S. L. Copper-catalyzed coupling of aryl iodides with aliphatic alcohols. Org. Lett. 4, 973-976 (2002).
    • (2002) Org. Lett. , vol.4 , pp. 973-976
    • Wolter, M.1    Nordmann, G.2    Job, G.E.3    Buchwald, S.L.4
  • 105
    • 1642378847 scopus 로고    scopus 로고
    • Theoretical studies on C-heteroatom bond formation via reductive elimination from group 10 M(PH3)2(CH3)(X) species (X = CH3, NH2, OH, SH) and the determination of metal-X bond strengths using density functional theory
    • Macgregor, S. A., Neave, G. W., Smith, C. Theoretical studies on C-heteroatom bond formation via reductive elimination from group 10 M(PH3)2(CH3)(X) species (X = CH3, NH2, OH, SH) and the determination of metal-X bond strengths using density functional theory. Faraday Discuss. 124, 111-127 (2003).
    • (2003) Faraday Discuss , vol.124 , pp. 111-127
    • MacGregor, S.A.1    Neave, G.W.2    Smith, C.3
  • 106
    • 84933060297 scopus 로고    scopus 로고
    • Aromatic methoxylation and hydroxylation by organometallic high-valent nickel complexes
    • Zhou, W., Schultz, J. W., Rath, N. P., Mirica, L. M. Aromatic methoxylation and hydroxylation by organometallic high-valent nickel complexes. J. Am. Chem. Soc. 137, 7604-7607 (2015).
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 7604-7607
    • Zhou, W.1    Schultz, J.W.2    Rath, N.P.3    Mirica, L.M.4
  • 107
    • 84939839315 scopus 로고    scopus 로고
    • Switching on elusive organometallic mechanisms with photoredox catalysis
    • Terrett, J. A., Cuthbertson, J. D., Shurtleff, V. W., MacMillan, D. W. C. Switching on elusive organometallic mechanisms with photoredox catalysis. Nature 524, 330-334 (2015).
    • (2015) Nature , vol.524 , pp. 330-334
    • Terrett, J.A.1    Cuthbertson, J.D.2    Shurtleff, V.W.3    MacMillan, D.W.C.4
  • 108
    • 57949109399 scopus 로고    scopus 로고
    • Halide ligands-more than just-donors A structural and spectroscopic study of homologous organonickel complexes
    • Klein, A. et al. Halide ligands-more than just-donors A structural and spectroscopic study of homologous organonickel complexes. Inorg. Chem. 47, 11324-11333 (2008).
    • (2008) Inorg. Chem. , vol.47 , pp. 11324-11333
    • Klein, A.1
  • 109
    • 85020670526 scopus 로고    scopus 로고
    • Photosensitized energy transfer-mediated organometallic catalysis through electronically excited nickel(II)
    • Welin, E. R., Le, C., Arias-Rotondo, D. M., McCusker, J. K., MacMillan, D. W. C. Photosensitized energy transfer-mediated organometallic catalysis through electronically excited nickel(ii). Science 355, 380-385 (2017).
    • (2017) Science , vol.355 , pp. 380-385
    • Welin Le, R.E.C.1    Arias-Rotondo, D.M.2    McCusker, J.K.3    MacMillan, D.W.C.4
  • 110
    • 33847031721 scopus 로고    scopus 로고
    • Photo-activation of Pd-catalyzed Sonogashira coupling using a Ru/bipyridine complex as energy transfer agent
    • Osawa, M., Nagai, H., Akita, M. Photo-activation of Pd-catalyzed Sonogashira coupling using a Ru/bipyridine complex as energy transfer agent. Dalton Trans. 8, 827-829 (2007).
    • (2007) Dalton Trans. , vol.8 , pp. 827-829
    • Osawa, M.1    Nagai, H.2    Akita, M.3
  • 111
    • 84937622429 scopus 로고    scopus 로고
    • Visible light-mediated Ullmann-type C-N coupling reactions of carbazole derivatives and aryl iodides
    • Yoo, W.-J., Tsukamoto, T., Kobayashi, S. Visible light-mediated Ullmann-type C-N coupling reactions of carbazole derivatives and aryl iodides. Org. Lett. 17, 3640-3642 (2015).
    • (2015) Org. Lett. , vol.17 , pp. 3640-3642
    • Yoo, W.-J.1    Tsukamoto, T.2    Kobayashi, S.3
  • 112
    • 84976908718 scopus 로고    scopus 로고
    • Aryl amination using ligand-free Ni(II) salts and photoredox catalysis
    • Corcoran, E. B. et al. Aryl amination using ligand-free Ni(ii) salts and photoredox catalysis. Science 353, 279-283 (2016).
    • (2016) Science , vol.353 , pp. 279-283
    • Corcoran, E.B.1
  • 113
    • 0030747792 scopus 로고    scopus 로고
    • Nickel-catalyzed amination of aryl chlorides
    • Wolfe, J. P., Buchwald, S. L. Nickel-catalyzed amination of aryl chlorides. J. Am. Chem. Soc. 119, 6054-6058 (1997).
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 6054-6058
    • Wolfe, J.P.1    Buchwald, S.L.2
  • 114
    • 39349098786 scopus 로고    scopus 로고
    • Nickel-catalyzed amination of aryl tosylates
    • Gao, C.-Y., Yang, L.-M. Nickel-catalyzed amination of aryl tosylates. J. Org. Chem. 73, 1624-1627 (2008).
    • (2008) J. Org. Chem. , vol.73 , pp. 1624-1627
    • Gao, C.-Y.1    Yang, L.-M.2
  • 115
    • 84891796806 scopus 로고    scopus 로고
    • Development of an air-stable nickel precatalyst for the amination of aryl chlorides, sulfamates, mesylates, and triflates
    • Park, N. H., Teverovskiy, G., Buchwald, S. L. Development of an air-stable nickel precatalyst for the amination of aryl chlorides, sulfamates, mesylates, and triflates. Org. Lett. 16, 220-223 (2014).
    • (2014) Org. Lett. , vol.16 , pp. 220-223
    • Park, N.H.1    Teverovskiy, G.2    Buchwald, S.L.3
  • 116
    • 84893445271 scopus 로고    scopus 로고
    • Controlling first-row catalysts: Amination of aryl and heteroaryl chlorides and bromides with primary aliphatic amines catalyzed by a BINAP-ligated single-component Ni(0) complex
    • Ge, S., Green, R. A., Hartwig, J. F. Controlling first-row catalysts: Amination of aryl and heteroaryl chlorides and bromides with primary aliphatic amines catalyzed by a BINAP-ligated single-component Ni(0) complex. J. Am. Chem. Soc. 136, 1617-1627 (2014).
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 1617-1627
    • Ge, S.1    Green, R.A.2    Hartwig, J.F.3
  • 117
    • 77950505239 scopus 로고    scopus 로고
    • Nickel-catalyzed amination of aryl pivalates by the cleavage of aryl C-O bonds
    • Shimasahi, T., Tobisu, M., Chatani, N. Nickel-catalyzed amination of aryl pivalates by the cleavage of aryl C-O bonds. Angew. Chem. Int. Ed. 49, 2929-2932 (2010).
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 2929-2932
    • Shimasahi, T.1    Tobisu, M.2    Chatani, N.3
  • 118
    • 84962323772 scopus 로고    scopus 로고
    • Challenging nickel-catalyzed amine arylations enabled by tailored ancillary ligand design
    • Lavoie, C. M. et al. Challenging nickel-catalyzed amine arylations enabled by tailored ancillary ligand design. Nat. Commun. 7, 11073 (2016).
    • (2016) Nat. Commun. , vol.7 , pp. 11073
    • Lavoie, C.M.1
  • 119
    • 52049105452 scopus 로고    scopus 로고
    • Biaryl phosphane ligands in palladium-catalyzed amination
    • Surry, D. S., Buchwald, S. L. Biaryl phosphane ligands in palladium-catalyzed amination. Angew. Chem. Int. Ed. 47, 6338-6361 (2008).
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 6338-6361
    • Surry, D.S.1    Buchwald, S.L.2
  • 120
    • 84962277993 scopus 로고    scopus 로고
    • Chemistry informer libraries: A cheminformatics enabled approach to evaluate and advance synthetic methods
    • Kutchukian, P. S. et al. Chemistry informer libraries: A cheminformatics enabled approach to evaluate and advance synthetic methods. Chem. Sci. 7, 2604-2613 (2016).
    • (2016) Chem. Sci. , vol.7 , pp. 2604-2613
    • Kutchukian, P.S.1
  • 121
    • 84938890238 scopus 로고    scopus 로고
    • Highly regioselective indoline synthesis under nickel/photoredox dual catalysis J
    • Tasker, S. Z., Jamison, T. F. Highly regioselective indoline synthesis under nickel/photoredox dual catalysis J. Am. Chem. Soc. 137, 9531-9534 (2015).
    • (2015) Am. Chem. Soc. , vol.137 , pp. 9531-9534
    • Tasker, S.Z.1    Jamison, T.F.2
  • 122
    • 84978766938 scopus 로고    scopus 로고
    • Highly chemoselective iridium photoredox and nickel catalysis for the cross-coupling of primary aryl amines with aryl halides
    • Oderinde, M. S. et al. Highly chemoselective iridium photoredox and nickel catalysis for the cross-coupling of primary aryl amines with aryl halides. Angew. Chem. Int. Ed. 55, 13219-13223 (2016).
    • (2016) Angew. Chem. Int. Ed. , vol.55 , pp. 13219-13223
    • Oderinde, M.S.1
  • 123
    • 84959010717 scopus 로고    scopus 로고
    • Photoredox mediated nickel catalyzed cross-coupling of thiols with aryl and heteroaryl iodides via thiyl radicals
    • Oderinde, M. S., Frenette, M., Robbins, D. W., Aquila, B., Johannes, J. M. Photoredox mediated nickel catalyzed cross-coupling of thiols with aryl and heteroaryl iodides via thiyl radicals. J. Am. Chem. Soc. 138, 1760-1763 (2016).
    • (2016) J. Am. Chem. Soc. , vol.138 , pp. 1760-1763
    • Oderinde, M.S.1    Frenette, M.2    Robbins, D.W.3    Aquila, B.4    Johannes, J.M.5
  • 124
    • 84959132380 scopus 로고    scopus 로고
    • Thioetherification via photoredox/nickel dual catalysis
    • Jouffroy, M., Kelly, C. B., Molander, G. A. Thioetherification via photoredox/nickel dual catalysis. Org. Lett. 18, 876-879 (2016).
    • (2016) Org. Lett. , vol.18 , pp. 876-879
    • Jouffroy, M.1    Kelly, C.B.2    Molander, G.A.3
  • 125
    • 84924574062 scopus 로고    scopus 로고
    • Room temperature C-P bond formation enabled by merging nickel catalysis and visible-light-induced photoredox catalysis
    • Xuan, J., Zeng, T.-T., Chen, J.-R., Lu, L.-Q., Xiao, W.-J. Room temperature C-P bond formation enabled by merging nickel catalysis and visible-light-induced photoredox catalysis. Chem. Eur. J. 21, 4962-4965 (2015).
    • (2015) Chem. Eur. J. , vol.21 , pp. 4962-4965
    • Xuan, J.1    Zeng, T.-T.2    Chen, J.-R.3    Lu, L.-Q.4    Xiao, W.-J.5
  • 126
    • 0037943974 scopus 로고    scopus 로고
    • Palladium-catalyzed alkynylation
    • Negishi, E.-I., Anastasia, L. Palladium-catalyzed alkynylation. Chem. Rev. 103, 1979-2017 (2003).
    • (2003) Chem. Rev. , vol.103 , pp. 1979-2017
    • Negishi, E.-I.1    Anastasia, L.2
  • 127
    • 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. 133, 18566-18569 (2011).
    • (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
  • 128
    • 19744365933 scopus 로고    scopus 로고
    • Oxidative C-H activation/C-C bond forming reactions: Synthetic scope and mechanistic insights
    • Kalyani, D., Deprez, N. R., Desai, L. V., Sanford, M. S. Oxidative C-H activation/C-C bond forming reactions: Synthetic scope and mechanistic insights. J. Am. Chem. Soc. 127, 7330-7331 (2005).
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 7330-7331
    • Kalyani, D.1    Deprez, N.R.2    Desai, L.V.3    Sanford, M.S.4
  • 129
    • 68249136644 scopus 로고    scopus 로고
    • Synthetic and mechanistic studies of Pd-catalyzed C-H arylation with diaryliodonium salts: Evidence for a bimetallic high oxidation state Pd intermediate
    • Deprez, N. R., Sanford, M. S. Synthetic and mechanistic studies of Pd-catalyzed C-H arylation with diaryliodonium salts: Evidence for a bimetallic high oxidation state Pd intermediate. J. Am. Chem. Soc. 131, 11234-11241 (2009).
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 11234-11241
    • Deprez, N.R.1    Sanford, M.S.2
  • 130
    • 68149126733 scopus 로고    scopus 로고
    • Palladium-catalyzed decarboxylative arylation of C-H bonds by aryl acylperoxides
    • Yu, W.-Y., Sit, W., Zhou, Z., Chan, A. S. C. Palladium-catalyzed decarboxylative arylation of C-H bonds by aryl acylperoxides. Org. Lett. 11, 3174-3177 (2009).
    • (2009) Org. Lett. , vol.11 , pp. 3174-3177
    • Yu, W.-Y.1    Sit, W.2    Zhou, Z.3    Chan, A.S.C.4
  • 131
    • 84885447567 scopus 로고    scopus 로고
    • Radical Pd(III)/Pd(i) reductive elimination in palladium sequences
    • Maestri, G., Malacria, M., Derat, E. Radical Pd(iii)/Pd(i) reductive elimination in palladium sequences. Chem. Commun. 49, 10424-10426 (2013).
    • (2013) Chem. Commun. , vol.49 , pp. 10424-10426
    • Maestri, G.1    Malacria, M.2    Derat, E.3
  • 133
    • 84983518040 scopus 로고    scopus 로고
    • Highly luminescent palladium(II) complexes with sub-millisecond blue to green phosphorescent excited states. Photocatalysis and highly efficient PSF-OLEDs
    • Chow, P.-K. et al. Highly luminescent palladium(ii) complexes with sub-millisecond blue to green phosphorescent excited states. Photocatalysis and highly efficient PSF-OLEDs. Chem. Sci. 7, 6083-6098 (2016).
    • (2016) Chem. Sci. , vol.7 , pp. 6083-6098
    • Chow, P.-K.1
  • 134
    • 84915782332 scopus 로고    scopus 로고
    • Synthesis of indoles using visible light: Photoredox catalysis for palladium-catalyzed C-H activation
    • Zoller, J., Fabry, D. C., Ronge, M. A., Rueping, M. Synthesis of indoles using visible light: Photoredox catalysis for palladium-catalyzed C-H activation. Angew. Chem. Int. Ed. 53, 13264-13268 (2014).
    • (2014) Angew. Chem. Int. Ed. , vol.53 , pp. 13264-13268
    • Zoller, J.1    Fabry, D.C.2    Ronge, M.A.3    Rueping, M.4
  • 135
    • 80054968939 scopus 로고    scopus 로고
    • Decarboxylative coupling reactions: A modern strategy for C-C bond formation
    • Rodriguez, N., Gooßen, L. J. Decarboxylative coupling reactions: A modern strategy for C-C bond formation. Chem. Soc. Rev. 40, 5030-5048 (2011).
    • (2011) Chem. Soc. Rev. , vol.40 , pp. 5030-5048
    • Rodriguez, N.1    Gooßen, L.J.2
  • 136
    • 84952701017 scopus 로고    scopus 로고
    • Merging photoredox with palladium catalysis: Decarboxylative ortho-acylation of acetanilides with-oxocarboxylic acids under mild reaction conditions
    • Zhou, C., Li, P., Zhu, X., Wang, L. Merging photoredox with palladium catalysis: Decarboxylative ortho-acylation of acetanilides with-oxocarboxylic acids under mild reaction conditions. Org. Lett. 17, 6198-6201 (2015).
    • (2015) Org. Lett. , vol.17 , pp. 6198-6201
    • Zhou, C.1    Li, P.2    Zhu, X.3    Wang, L.4
  • 137
    • 84956928715 scopus 로고    scopus 로고
    • Merging visible-light photocatalysis with palladium catalysis for C-H acylation of azo-and azoxybenzenes with-keto acids
    • Xu, N., Li, P., Xie, Z., Wang, L. Merging visible-light photocatalysis with palladium catalysis for C-H acylation of azo-and azoxybenzenes with-keto acids. Chem. Eur. J. 22, 2236-2242 (2016).
    • (2016) Chem. Eur. J. , vol.22 , pp. 2236-2242
    • Xu, N.1    Li, P.2    Xie, Z.3    Wang, L.4
  • 138
    • 84940900259 scopus 로고    scopus 로고
    • Room-temperature decarboxylative couplings of-oxocarboxylates with aryl halides by merging photoredox with palladium catalysis
    • Cheng, W.-M., Shang, R., Yu, H.-Z., Fu, Y. Room-temperature decarboxylative couplings of-oxocarboxylates with aryl halides by merging photoredox with palladium catalysis. Chem. Eur. J. 21, 13191-13195 (2015).
    • (2015) Chem. Eur. J. , vol.21 , pp. 13191-13195
    • Cheng, W.-M.1    Shang, R.2    Yu, H.-Z.3    Fu, Y.4
  • 139
    • 84949115462 scopus 로고    scopus 로고
    • Decarboxylative allylation of amino alkanoic acids and esters via dual catalysis
    • Lang, S. B., O'Nele, K. M., Tunge, J. A. Decarboxylative allylation of amino alkanoic acids and esters via dual catalysis. J. Am. Chem. Soc. 136, 13606-13609 (2014).
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 13606-13609
    • Lang, S.B.1    O'Nele, K.M.2    Tunge, J.A.3
  • 140
    • 84954403460 scopus 로고    scopus 로고
    • Dual catalytic decarboxylative allylations of-amino acids and their divergent mechanisms
    • Lang, S. B., O'Nele, K. M., Tunge, J. A. Dual catalytic decarboxylative allylations of-amino acids and their divergent mechanisms. Chem. Eur. J. 21, 18589-18593 (2015).
    • (2015) Chem. Eur. J. , vol.21 , pp. 18589-18593
    • Lang, S.B.1    O'Nele, K.M.2    Tunge, J.A.3
  • 141
    • 84921446114 scopus 로고    scopus 로고
    • Redox-neutral-allylation of amines by combining palladium catalysis and visible-light photoredox catalysis
    • Xuan, J. et al. Redox-neutral-allylation of amines by combining palladium catalysis and visible-light photoredox catalysis. Angew. Chem. Int. Ed. 54, 1625-1628 (2015).
    • (2015) Angew. Chem. Int. Ed. , vol.54 , pp. 1625-1628
    • Xuan, J.1
  • 142
    • 84861863992 scopus 로고    scopus 로고
    • Merging visible-light photocatalysis and transition-metal catalysis in the copper-catalyzed trifluoromethylation of boronic acids with CF3I
    • Ye, Y., Sanford, M. S. Merging visible-light photocatalysis and transition-metal catalysis in the copper-catalyzed trifluoromethylation of boronic acids with CF3I. J. Am. Chem. Soc. 134, 9034-9037 (2012).
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 9034-9037
    • Ye, Y.1    Sanford, M.S.2
  • 144
    • 68249144236 scopus 로고    scopus 로고
    • Enantioselective-trifluoromethylation of aldehydes via photoredox organocatalysis
    • Nagib, D. A., Scott, M. E., MacMillan, D. W. C. Enantioselective-trifluoromethylation of aldehydes via photoredox organocatalysis. J. Am. Chem. Soc. 131, 10875-10877 (2009).
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 10875-10877
    • Nagib, D.A.1    Scott, M.E.2    MacMillan, D.W.C.3
  • 145
    • 85027957723 scopus 로고    scopus 로고
    • Visible-light-mediated Chan-Lam coupling reactions of aryl boronic acids and aniline derivatives
    • Yoo, W.-J., Tsukamoto, T., Kobayashi, S. Visible-light-mediated Chan-Lam coupling reactions of aryl boronic acids and aniline derivatives. Angew. Chem. Int. Ed. 54, 6587-6590 (2015).
    • (2015) Angew. Chem. Int. Ed. , vol.54 , pp. 6587-6590
    • Yoo, W.-J.1    Tsukamoto, T.2    Kobayashi, S.3
  • 146
    • 0035963683 scopus 로고    scopus 로고
    • Copper-catalyzed coupling of arylboronic acids and amines
    • Antilla, J. C., Buchwald, S. L. Copper-catalyzed coupling of arylboronic acids and amines. Org. Lett. 3, 2077-2079 (2001).
    • (2001) Org. Lett. , vol.3 , pp. 2077-2079
    • Antilla, J.C.1    Buchwald, S.L.2
  • 147
    • 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. 132, 1474-1475 (2010).
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 1474-1475
    • Zhang, G.1    Cui, L.2    Wang, Y.3    Zhang, L.4
  • 148
    • 78049522167 scopus 로고    scopus 로고
    • Gold-catalyzed cascade cyclization-oxidative alkynylation of allenoates
    • Hopkinson, M. N., Ross, J. E., Giuffredi, G. T., Gee, A. D., Gouverneur, V. Gold-catalyzed cascade cyclization-oxidative alkynylation of allenoates. Org. Lett. 12, 4904-4907 (2010).
    • (2010) Org. Lett. , vol.12 , pp. 4904-4907
    • Hopkinson, M.N.1    Ross, J.E.2    Giuffredi, G.T.3    Gee, A.D.4    Gouverneur, V.5
  • 149
    • 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. 132, 8885-8887 (2010).
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 8885-8887
    • Melhado, A.D.1    Brenzovich, W.E.2    Lackner, A.D.3    Toste, F.D.4
  • 150
    • 84857591083 scopus 로고    scopus 로고
    • Gold-catalyzed oxyarylation of styrenes and mono-and gem-disubstituted olefins facilitated by an iodine (III) oxidant
    • Ball, L. T., Lloyd-Jones, G. C., Russell, C. A. Gold-catalyzed oxyarylation of styrenes and mono-and gem-disubstituted olefins facilitated by an iodine (iii) oxidant. Chem. Eur. J. 18, 2931-2937 (2012).
    • (2012) Chem. Eur. J. , vol.18 , pp. 2931-2937
    • Ball, L.T.1    Lloyd-Jones, G.C.2    Russell, C.A.3
  • 151
    • 84908433260 scopus 로고    scopus 로고
    • Facile oxidative addition of aryl iodides to gold(i) by ligand design: Bending turns on reactivity
    • Joost, M. et al. Facile oxidative addition of aryl iodides to gold(i) by ligand design: Bending turns on reactivity. J. Am. Chem. Soc. 136, 14654-14657 (2014).
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 14654-14657
    • Joost, M.1
  • 153
    • 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 517, 449-454 (2015).
    • (2015) Nature , vol.517 , pp. 449-454
    • Wu, C.-Y.1    Horibe, T.2    Jacobsen, C.B.3    Toste, F.D.4
  • 154
    • 84991784019 scopus 로고    scopus 로고
    • Merging visible light photoredox and gold catalysis
    • Hopkinson, M. N., Tlahuext-Aca, A., Glorius, F. Merging visible light photoredox and gold catalysis. Acc. Chem. Res. 49, 2261-2272 (2016).
    • (2016) Acc. Chem. Res. , vol.49 , pp. 2261-2272
    • Hopkinson, M.N.1    Tlahuext-Aca, A.2    Glorius, F.3
  • 155
    • 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. 7, 89-93 (2016).
    • (2016) Chem. Sci. , vol.7 , pp. 89-93
    • Tlahuext-Aca, A.1    Hopkinson, M.N.2    Sahoo, B.3    Glorius, F.4
  • 156
    • 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. 22, 11587-11592 (2016).
    • (2016) Chem. Eur. J. , vol.22 , pp. 11587-11592
    • Tlahuext-Aca, A.1    Hopkinson, M.N.2    Daniliuc, C.G.3    Glorius, F.4
  • 157
    • 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. 135, 5505-5508 (2013).
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 5505-5508
    • Sahoo, B.1    Hopkinson, M.N.2    Glorius, F.3
  • 158
    • 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. 6, 798-808 (2016).
    • (2016) ACS Catal. , vol.6 , pp. 798-808
    • Zhang, Q.1    Zhang, Z.-Q.2    Fu, Y.3    Yu, H.-Z.4
  • 159
    • 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. 356, 2794-2800 (2014).
    • (2014) Adv. Synth. Catal. , vol.356 , pp. 2794-2800
    • Hopkinson, M.N.1    Sahoo, B.2    Glorius, F.3
  • 160
    • 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. 136, 5844-5847 (2014).
    • (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
  • 161
    • 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. 357, 2622-2628 (2015).
    • (2015) Adv. Synth. Catal. , vol.357 , pp. 2622-2628
    • Patil, D.V.1    Yun, H.2    Shin, S.3
  • 162
    • 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. 18, 484-487 (2016).
    • (2016) Org. Lett. , vol.18 , pp. 484-487
    • Um, J.1    Yun, H.2    Shin, S.3
  • 163
    • 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. 358, 1526-1533 (2016).
    • (2016) Adv. Synth. Catal. , vol.358 , pp. 1526-1533
    • Alcaide, B.1    Almendros, P.2    Busto, E.3    Luna, A.4
  • 165
    • 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. 55, 4808-4813 (2016).
    • (2016) Angew. Chem. Int. Ed. , vol.55 , pp. 4808-4813
    • Huang, L.1    Rudolph, M.2    Rominger, F.3    Hashmi, A.S.K.4
  • 166
    • 84951194469 scopus 로고    scopus 로고
    • Visible light-mediated gold-catalysed carbon(sp2)-carbon(sp) coupling
    • Kim, S., Rojas-Martin, J., Toste, F. D. Visible light-mediated gold-catalysed carbon(sp2)-carbon(sp) coupling. Chem. Sci. 7, 85-88 (2016).
    • (2016) Chem. Sci. , vol.7 , pp. 85-88
    • Kim, S.1    Rojas-Martin, J.2    Toste, F.D.3
  • 167
    • 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. 52, 10040-10043 (2016).
    • (2016) Chem. Commun. , vol.52 , pp. 10040-10043
    • Cornilleau, T.1    Hermange, P.2    Fouquet, E.3
  • 168
    • 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. 52, 10163-10166 (2016).
    • (2016) Chem. Commun. , vol.52 , pp. 10163-10166
    • Gauchot, V.1    Lee, A.-L.2
  • 169
    • 84921341133 scopus 로고    scopus 로고
    • A dual catalytic strategy for carbon-phosphorous cross-coupling via gold and photoredox catalysis
    • He, Y., Wu, H., Toste, F. D. A dual catalytic strategy for carbon-phosphorous cross-coupling via gold and photoredox catalysis. Chem. Sci. 6, 1194-1198 (2015).
    • (2015) Chem. Sci. , vol.6 , pp. 1194-1198
    • He, Y.1    Wu, H.2    Toste, F.D.3
  • 170
    • 85027954273 scopus 로고    scopus 로고
    • Combining rhodium and photoredox catalysis for C-H bond functionalization of arenes: Oxidative Heck reactions with visible light
    • Fabry, D. C., Zoller, J., Raja, S., Rueping, M. Combining rhodium and photoredox catalysis for C-H bond functionalization of arenes: Oxidative Heck reactions with visible light. Angew. Chem. Int. Ed. 53, 10228-10231 (2014).
    • (2014) Angew. Chem. Int. Ed. , vol.53 , pp. 10228-10231
    • Fabry, D.C.1    Zoller, J.2    Raja, S.3    Rueping, M.4
  • 171
    • 84923106044 scopus 로고    scopus 로고
    • C-H functionalization of phenols using combined ruthenium and photoredox catalysis: In situ generation of the oxidant
    • Fabry, D. C., Ronge, M. A., Zoller, J., Rueping, M. C-H functionalization of phenols using combined ruthenium and photoredox catalysis: In situ generation of the oxidant. Angew. Chem. Int. Ed. 54, 2801-2805 (2015).
    • (2015) Angew. Chem. Int. Ed. , vol.54 , pp. 2801-2805
    • Fabry, D.C.1    Ronge, M.A.2    Zoller, J.3    Rueping, M.4
  • 172
    • 84938400357 scopus 로고    scopus 로고
    • External oxidant-free oxidative cross-coupling: A photoredox cobalt-catalyzed aromatic C-H thiolation for constructing C-S bonds
    • Zhang, G. et al. External oxidant-free oxidative cross-coupling: A photoredox cobalt-catalyzed aromatic C-H thiolation for constructing C-S bonds. J. Am. Chem. Soc. 137, 9273-9280 (2015).
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 9273-9280
    • Zhang, G.1
  • 173
    • 84898734503 scopus 로고    scopus 로고
    • Cross-coupling hydrogen evolution reaction in homogenous solution without noble metals
    • Zhong, J.-J. et al. Cross-coupling hydrogen evolution reaction in homogenous solution without noble metals. Org. Lett. 16, 1988-1991 (2014).
    • (2014) Org. Lett. , vol.16 , pp. 1988-1991
    • Zhong, J.-J.1
  • 174
    • 84927130955 scopus 로고    scopus 로고
    • Visible light catalysis assisted site-specific functionalization of amino acid derivatives by C-H bond activation with oxidant: Cross-coupling hydrogen evolution reaction
    • Gao, X.-W. et al. Visible light catalysis assisted site-specific functionalization of amino acid derivatives by C-H bond activation with oxidant: Cross-coupling hydrogen evolution reaction. ACS Catal. 5, 2391-2396 (2015).
    • (2015) ACS Catal. , vol.5 , pp. 2391-2396
    • Gao, X.-W.1
  • 175
    • 84941061451 scopus 로고    scopus 로고
    • A cascade cross-coupling and in situ hydrogenation reaction by visible light catalysis
    • Zhong, J.-J. et al. A cascade cross-coupling and in situ hydrogenation reaction by visible light catalysis. Adv. Synth. Catal. 356, 2846-2852 (2014).
    • (2014) Adv. Synth. Catal. , vol.356 , pp. 2846-2852
    • Zhong, J.-J.1
  • 176
    • 84949057452 scopus 로고    scopus 로고
    • Activation of C-H bonds through oxidant-free photoredox cataysis: Cross-coupling hydrogen-evolution transformation of isochromans and-keto esters
    • Xiang, M. et al. Activation of C-H bonds through oxidant-free photoredox cataysis: Cross-coupling hydrogen-evolution transformation of isochromans and-keto esters. Chem. Eur. J. 21, 18080-18084 (2015).
    • (2015) Chem. Eur. J. , vol.21 , pp. 18080-18084
    • Xiang, M.1
  • 177
    • 84977137165 scopus 로고    scopus 로고
    • An oxidant-free strategy for indole synthesis via intramolecular C-C bond construction under visible light irradiation: Cross-coupling hydrogen evolution reaction
    • Wu, C.-J. et al. An oxidant-free strategy for indole synthesis via intramolecular C-C bond construction under visible light irradiation: Cross-coupling hydrogen evolution reaction. ACS Catal. 6, 4635-4639 (2016).
    • (2016) ACS Catal. , vol.6 , pp. 4635-4639
    • Wu, C.-J.1
  • 178
    • 77953908642 scopus 로고    scopus 로고
    • [2+2] cycloadditions by oxidative visible light photocatalysis
    • Ischay, M. A., Lu, Z., Yoon, T. P. [2+2] cycloadditions by oxidative visible light photocatalysis. J. Am. Chem. Soc. 132, 8572-8574 (2010).
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 8572-8574
    • Ischay, M.A.1    Lu, Z.2    Yoon, T.P.3
  • 179
    • 82555175889 scopus 로고    scopus 로고
    • Radical cation Diels-Alder cycloadditions by visible light photocatalysis
    • Lin, S., Ischay, M. A., Fry, C. G., Yoon, T. Radical cation Diels-Alder cycloadditions by visible light photocatalysis. J. Am. Chem. Soc. 133, 19350-19353 (2011).
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 19350-19353
    • Lin, S.1    Ischay, M.A.2    Fry, C.G.3    Yoon, T.4
  • 180
    • 84988494725 scopus 로고    scopus 로고
    • A general approach to catalytic alkene anti-Markovnikov hydrofunctionalization reactions via acridinium photoredox catalysis
    • Margrey, K. A., Nicewicz, D. A. A general approach to catalytic alkene anti-Markovnikov hydrofunctionalization reactions via acridinium photoredox catalysis. Acc. Chem. Res. 49, 1997-2006 (2016).
    • (2016) Acc. Chem. Res. , vol.49 , pp. 1997-2006
    • Margrey, K.A.1    Nicewicz, D.A.2
  • 181
    • 85006993937 scopus 로고    scopus 로고
    • Photocatalytic dehydrogenative cross-coupling of alkenes with alcohols or azoles without external oxidant
    • Yi, H. et al. Photocatalytic dehydrogenative cross-coupling of alkenes with alcohols or azoles without external oxidant. Angew. Chem. Int. Ed. 56, 1120-1124 (2017).
    • (2017) Angew. Chem. Int. Ed. , vol.56 , pp. 1120-1124
    • Yi, H.1
  • 182
    • 84988566074 scopus 로고    scopus 로고
    • Anti-Markovnikov oxidation of-alkyl styrenes with H2O as the terminal oxidant
    • Zhang, G. et al. Anti-Markovnikov oxidation of-alkyl styrenes with H2O as the terminal oxidant. J. Am. Chem. Soc. 138, 12037-12040 (2016).
    • (2016) J. Am. Chem. Soc. , vol.138 , pp. 12037-12040
    • Zhang, G.1
  • 183
    • 85014554611 scopus 로고    scopus 로고
    • Acceptorless dehydrogenation of N-heterocycles by merging visible-light photoredox catalysis and cobalt catalysis
    • He, K.-H. et al. Acceptorless dehydrogenation of N-heterocycles by merging visible-light photoredox catalysis and cobalt catalysis. Angew. Chem. Int. Ed. 56, 3080-3084 (2017).
    • (2017) Angew. Chem. Int. Ed. , vol.56 , pp. 3080-3084
    • He, K.-H.1


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