-
1
-
-
0036570496
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
39
-
-
78650383080
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
132
-
-
77957718126
-
Bimetallic reductive elimination from dinuclear Pd(III) complexes
-
Powers, D. C., Benitez, D., Tkatchouk, E., Goddard, W. A., Ritter, T. Bimetallic reductive elimination from dinuclear Pd(iii) complexes. J. Am. Chem. Soc. 132, 14092-14103 (2010).
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 14092-14103
-
-
Powers, D.C.1
Benitez, D.2
Tkatchouk, E.3
Goddard, W.A.4
Ritter, T.5
-
133
-
-
84983518040
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
143
-
-
38149070200
-
Fluorine in medicinal chemistry
-
Purser, S., Moore, P. R., Swallow, S., Gouverneur, V. Fluorine in medicinal chemistry. Chem. Soc. Rev. 37, 320-330 (2008).
-
(2008)
Chem. Soc. Rev.
, vol.37
, pp. 320-330
-
-
Purser, S.1
Moore, P.R.2
Swallow, S.3
Gouverneur, V.4
-
144
-
-
68249144236
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
152
-
-
85027956394
-
Oxidative addition of carbon-carbon bonds to gold
-
Joost, M., Estévez, L., Miqueu, K., Amgoune, A., Bourissou, D. Oxidative addition of carbon-carbon bonds to gold. Angew. Chem. Int. Ed. 54, 5236-5240 (2015).
-
(2015)
Angew. Chem. Int. Ed.
, vol.54
, pp. 5236-5240
-
-
Joost, M.1
Estévez, L.2
Miqueu, K.3
Amgoune, A.4
Bourissou, D.5
-
153
-
-
84922998686
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
164
-
-
84960145256
-
Alkyne difunctionalization by dual gold/photoredox catalysis
-
Tlahuext-Aca, A., Hopkinson, M. N., Garza-Sanchez, R. A., Glorius, F. Alkyne difunctionalization by dual gold/photoredox catalysis. Chem. Eur. J. 22, 5909-5913 (2016).
-
(2016)
Chem. Eur. J.
, vol.22
, pp. 5909-5913
-
-
Tlahuext-Aca, A.1
Hopkinson, M.N.2
Garza-Sanchez, R.A.3
Glorius, F.4
-
165
-
-
84960510911
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
[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
-
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
-
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
-
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
-
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
-
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
|