-
1
-
-
85029677016
-
-
For selected reviews on visible-light photoredox catalysis
-
For selected reviews on visible-light photoredox catalysis:
-
-
-
-
4
-
-
84903317897
-
-
Angew. Chem. 2012, 124, 6934;
-
(2012)
Angew. Chem.
, vol.124
, pp. 6934
-
-
-
6
-
-
84983344352
-
-
M. H. Shaw, J. Twilton, D. W. C. MacMillan, J. Org. Chem. 2016, 81, 6898.
-
(2016)
J. Org. Chem.
, vol.81
, pp. 6898
-
-
Shaw, M.H.1
Twilton, J.2
MacMillan, D.W.C.3
-
7
-
-
84933059650
-
-
G. J. S. Dawes, E. L. Scott, J. Le Nôtre, J. P. M. Sanders, J. H. Bitter, Green Chem. 2015, 17, 3231;
-
(2015)
Green Chem.
, vol.17
, pp. 3231
-
-
Dawes, G.J.S.1
Scott, E.L.2
Le Nôtre, J.3
Sanders, J.P.M.4
Bitter, J.H.5
-
8
-
-
84978890735
-
-
G. Yang, C. Zhu, X. Zou, L. Zhou, Sci. Rep. 2016, 6, 29711.
-
(2016)
Sci. Rep.
, vol.6
, pp. 29711
-
-
Yang, G.1
Zhu, C.2
Zou, X.3
Zhou, L.4
-
9
-
-
84905674432
-
-
L. Chu, C. Ohta, Z. Zuo, D. W. C. MacMillan, J. Am. Chem. Soc. 2014, 136, 10886;
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 10886
-
-
Chu, L.1
Ohta, C.2
Zuo, Z.3
MacMillan, D.W.C.4
-
10
-
-
84928963782
-
-
S. Ventre, F. R. Petronijevic, D. W. C. MacMillan, J. Am. Chem. Soc. 2015, 137, 5654;
-
(2015)
J. Am. Chem. Soc.
, vol.137
, pp. 5654
-
-
Ventre, S.1
Petronijevic, F.R.2
MacMillan, D.W.C.3
-
11
-
-
84941242136
-
-
J. D. Griffin, M. A. Zeller, D. A. Nicewicz, J. Am. Chem. Soc. 2015, 137, 11340;
-
(2015)
J. Am. Chem. Soc.
, vol.137
, pp. 11340
-
-
Griffin, J.D.1
Zeller, M.A.2
Nicewicz, D.A.3
-
12
-
-
84982303783
-
-
C. P. Johnston, R. T. Smith, S. Allmendinger, D. W. C. MacMillan, Nature 2016, 536, 322;
-
(2016)
Nature
, vol.536
, pp. 322
-
-
Johnston, C.P.1
Smith, R.T.2
Allmendinger, S.3
MacMillan, D.W.C.4
-
13
-
-
84959440380
-
-
L. Candish, L. Pitzer, A. Gómez-Suárez, F. Glorius, Chem. Eur. J. 2016, 22, 4753;
-
(2016)
Chem. Eur. J.
, vol.22
, pp. 4753
-
-
Candish, L.1
Pitzer, L.2
Gómez-Suárez, A.3
Glorius, F.4
-
14
-
-
84973577795
-
-
L. Candish, E. A. Standley, A. Gómez-Suárez, S. Mukherjee, F. Glorius, Chem. Eur. J. 2016, 22, 9971.
-
(2016)
Chem. Eur. J.
, vol.22
, pp. 9971
-
-
Candish, L.1
Standley, E.A.2
Gómez-Suárez, A.3
Mukherjee, S.4
Glorius, F.5
-
15
-
-
0001476677
-
-
K. Okada, K. Okamoto, N. Morita, K. Okubo, M. Oda, J. Am. Chem. Soc. 1991, 113, 9401;
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 9401
-
-
Okada, K.1
Okamoto, K.2
Morita, N.3
Okubo, K.4
Oda, M.5
-
17
-
-
84969435032
-
-
Angew. Chem. 2012, 124, 9714;
-
(2012)
Angew. Chem.
, vol.124
, pp. 9714
-
-
-
18
-
-
85020430813
-
-
L. Candish, M. Teders, F. Glorius, J. Am. Chem. Soc. 2017, 139, 7440;
-
(2017)
J. Am. Chem. Soc.
, vol.139
, pp. 7440
-
-
Candish, L.1
Teders, M.2
Glorius, F.3
-
19
-
-
85013149739
-
-
W. F. Petersen, R. J. K. Taylor, J. R. Donald, Org. Lett. 2017, 19, 874;
-
(2017)
Org. Lett.
, vol.19
, pp. 874
-
-
Petersen, W.F.1
Taylor, R.J.K.2
Donald, J.R.3
-
20
-
-
85013455450
-
-
A. Tlahuext-Aca, R. A. Garza-Sanchez, F. Glorius, Angew. Chem. Int. Ed. 2017, 56, 3708;
-
(2017)
Angew. Chem. Int. Ed.
, vol.56
, pp. 3708
-
-
Tlahuext-Aca, A.1
Garza-Sanchez, R.A.2
Glorius, F.3
-
21
-
-
85024407387
-
-
Angew. Chem. 2017, 129, 3762;
-
(2017)
Angew. Chem.
, vol.129
, pp. 3762
-
-
-
22
-
-
85019394289
-
-
D. Hu, L. Wang, P. Li, Org. Lett. 2017, 19, 2770.
-
(2017)
Org. Lett.
, vol.19
, pp. 2770
-
-
Hu, D.1
Wang, L.2
Li, P.3
-
23
-
-
84964558188
-
-
T. Qin, J. Cornella, C. Li, L. R. Malins, J. T. Edwards, S. Kawamura, B. D. Maxwell, M. D. Eastgate, P. S. Baran, Science 2016, 352, 801;
-
(2016)
Science
, vol.352
, pp. 801
-
-
Qin, T.1
Cornella, J.2
Li, C.3
Malins, L.R.4
Edwards, J.T.5
Kawamura, S.6
Maxwell, B.D.7
Eastgate, M.D.8
Baran, P.S.9
-
24
-
-
84966292281
-
-
K. M. M. Huihui, J. A. Caputo, Z. Melchor, A. M. Olivares, A. M. Spiewak, K. A. Johnson, T. A. DiBenedetto, S. Kim, L. K. G. Ackerman, D. J. Weix, J. Am. Chem. Soc. 2016, 138, 5016;
-
(2016)
J. Am. Chem. Soc.
, vol.138
, pp. 5016
-
-
Huihui, K.M.M.1
Caputo, J.A.2
Melchor, Z.3
Olivares, A.M.4
Spiewak, A.M.5
Johnson, K.A.6
DiBenedetto, T.A.7
Kim, S.8
Ackerman, L.K.G.9
Weix, D.J.10
-
25
-
-
85019263794
-
-
J. T. Edwards, R. R. Merchant, K. S. McClymont, K. W. Knouse, T. Qin, L. R. Malins, B. Vokits, S. A. Shaw, D.-H. Bao, F.-L. Wei, T. Zhou, M. D. Eastgate, P. S. Baran, Nature 2017, 545, 213;
-
(2017)
Nature
, vol.545
, pp. 213
-
-
Edwards, J.T.1
Merchant, R.R.2
McClymont, K.S.3
Knouse, K.W.4
Qin, T.5
Malins, L.R.6
Vokits, B.7
Shaw, S.A.8
Bao, D.-H.9
Wei, F.-L.10
Zhou, T.11
Eastgate, M.D.12
Baran, P.S.13
-
26
-
-
85017660132
-
-
C. Li, J. Wang, L. M. Barton, S. Yu, M. Tian, D. S. Peters, M. Kumar, A. W. Yu, K. A. Johnson, A. K. Chatterjee, M. Yan, P. S. Baran, Science 2017, https://doi.org/10.1126/science.aam7355;
-
, vol.2017
-
-
Li, C.1
Wang, J.2
Barton, L.M.3
Yu, S.4
Tian, M.5
Peters, D.S.6
Kumar, M.7
Yu, A.W.8
Johnson, K.A.9
Chatterjee, A.K.10
Yan, M.11
Baran, P.S.12
-
27
-
-
85018461160
-
-
N. Suzuki, J. L. Hofstra, K. E. Poremba, S. E. Reisman, Org. Lett. 2017, 19, 2150.
-
(2017)
Org. Lett.
, vol.19
, pp. 2150
-
-
Suzuki, N.1
Hofstra, J.L.2
Poremba, K.E.3
Reisman, S.E.4
-
28
-
-
34547421751
-
-
E. Scott, F. Peter, J. Sanders, Appl. Microbiol. Biotechnol. 2007, 75, 751.
-
(2007)
Appl. Microbiol. Biotechnol.
, vol.75
, pp. 751
-
-
Scott, E.1
Peter, F.2
Sanders, J.3
-
30
-
-
84959431895
-
-
Q. Wang, Y. Su, L. Li, H. Huang, Chem. Soc. Rev. 2016, 45, 1257.
-
(2016)
Chem. Soc. Rev.
, vol.45
, pp. 1257
-
-
Wang, Q.1
Su, Y.2
Li, L.3
Huang, H.4
-
31
-
-
84908451913
-
-
T. P. T. Cushnie, B. Cushnie, A. J. Lamb, Int. J. Antimicrob. Agents 2014, 44, 377.
-
(2014)
Int. J. Antimicrob. Agents
, vol.44
, pp. 377
-
-
Cushnie, T.P.T.1
Cushnie, B.2
Lamb, A.J.3
-
32
-
-
78650122737
-
-
N. A. McGrath, M. Brichacek, J. T. Njardarson, J. Chem. Educ. 2010, 87, 1348.
-
(2010)
J. Chem. Educ.
, vol.87
, pp. 1348
-
-
McGrath, N.A.1
Brichacek, M.2
Njardarson, J.T.3
-
34
-
-
84999015188
-
-
V. Froidevaux, C. Negrell, S. Caillol, J.-P. Pascault, B. Boutevin, Chem. Rev. 2016, 116, 14181.
-
(2016)
Chem. Rev.
, vol.116
, pp. 14181
-
-
Froidevaux, V.1
Negrell, C.2
Caillol, S.3
Pascault, J.-P.4
Boutevin, B.5
-
35
-
-
0003875430
-
-
A. R. Katritzky, U. Gruntz, D. H. Kenny, M. C. Rezende, H. Sheikh, J. Chem. Soc. Perkin Trans. 1 1979, 430.
-
(1979)
J. Chem. Soc. Perkin Trans. 1
, pp. 430
-
-
Katritzky, A.R.1
Gruntz, U.2
Kenny, D.H.3
Rezende, M.C.4
Sheikh, H.5
-
36
-
-
85018473113
-
-
C. H. Basch, J. Liao, J. Xu, J. J. Piane, M. P. Watson, J. Am. Chem. Soc. 2017, 139, 5313.
-
(2017)
J. Am. Chem. Soc.
, vol.139
, pp. 5313
-
-
Basch, C.H.1
Liao, J.2
Xu, J.3
Piane, J.J.4
Watson, M.P.5
-
37
-
-
0346222306
-
-
J. Grimshaw, S. Moore, J. T. Grimshaw, Acta Chem. Scand. Ser. B 1983, 37, 485.
-
(1983)
Acta Chem. Scand. Ser. B
, vol.37
, pp. 485
-
-
Grimshaw, J.1
Moore, S.2
Grimshaw, J.T.3
-
38
-
-
85029679245
-
-
For examples, see
-
Current methods for the generation of carbon-centered radicals via the cleavage of C−N bonds are mostly limited to the single-electron reduction of aryl diazonium salts. For examples, see:
-
-
-
-
39
-
-
85029725052
-
-
Y. Su, L. Zhang, N. Jiao, Org. Lett. 2011, 13, 2169;
-
(2011)
Org. Lett.
, vol.13
, pp. 2169
-
-
Su, Y.1
Zhang, L.2
Jiao, N.3
-
40
-
-
84856823966
-
-
D. P. Hari, P. Scholl, B. König, J. Am. Chem. Soc. 2012, 134, 2958;
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 2958
-
-
Hari, D.P.1
Scholl, P.2
König, B.3
-
41
-
-
84876487932
-
-
B. Sahoo, M. N. Hopkinson, F. Glorius, J. Am. Chem. Soc. 2013, 135, 5505;
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 5505
-
-
Sahoo, B.1
Hopkinson, M.N.2
Glorius, F.3
-
42
-
-
84951197056
-
-
A. Tlahuext-Aca, M. N. Hopkinson, B. Sahoo, F. Glorius, Chem. Sci. 2016, 7, 89.
-
(2016)
Chem. Sci.
, vol.7
, pp. 89
-
-
Tlahuext-Aca, A.1
Hopkinson, M.N.2
Sahoo, B.3
Glorius, F.4
-
43
-
-
84921285045
-
-
For a related example of N−N bond cleavage, see
-
For a related example of N−N bond cleavage, see: T. W. Greulich, C. G. Daniliuc, A. Studer, Org. Lett. 2015, 17, 254.
-
(2015)
Org. Lett.
, vol.17
, pp. 254
-
-
Greulich, T.W.1
Daniliuc, C.G.2
Studer, A.3
-
44
-
-
84960370396
-
-
M. N. Hopkinson, A. Gomez-Suarez, M. Teders, B. Sahoo, F. Glorius, Angew. Chem. Int. Ed. 2016, 55, 4361;
-
(2016)
Angew. Chem. Int. Ed.
, vol.55
, pp. 4361
-
-
Hopkinson, M.N.1
Gomez-Suarez, A.2
Teders, M.3
Sahoo, B.4
Glorius, F.5
-
45
-
-
85008898735
-
-
Angew. Chem. 2016, 128, 4434;
-
(2016)
Angew. Chem.
, vol.128
, pp. 4434
-
-
-
46
-
-
85008893142
-
-
M. Teders, A. Gomez-Suarez, L. Pitzer, M. N. Hopkinson, F. Glorius, Angew. Chem. Int. Ed. 2017, 56, 902;
-
(2017)
Angew. Chem. Int. Ed.
, vol.56
, pp. 902
-
-
Teders, M.1
Gomez-Suarez, A.2
Pitzer, L.3
Hopkinson, M.N.4
Glorius, F.5
-
47
-
-
85029721241
-
-
Angew. Chem. 2017, 129, 921.
-
(2017)
Angew. Chem.
, vol.129
, pp. 921
-
-
-
49
-
-
84870541226
-
-
Y. Fujiwara, J. A. Dixon, F. O'Hara, E. D. Funder, D. D. Dixon, R. A. Rodriguez, R. D. Baxter, B. Herle, N. Sach, M. R. Collins, Y. Ishihara, P. S. Baran, Nature 2012, 492, 95;
-
(2012)
Nature
, vol.492
, pp. 95
-
-
Fujiwara, Y.1
Dixon, J.A.2
O'Hara, F.3
Funder, E.D.4
Dixon, D.D.5
Rodriguez, R.A.6
Baxter, R.D.7
Herle, B.8
Sach, N.9
Collins, M.R.10
Ishihara, Y.11
Baran, P.S.12
-
50
-
-
84899936504
-
-
D. A. DiRocco, K. Dykstra, S. Krska, P. Vachal, D. V. Conway, M. Tudge, Angew. Chem. Int. Ed. 2014, 53, 4802;
-
(2014)
Angew. Chem. Int. Ed.
, vol.53
, pp. 4802
-
-
DiRocco, D.A.1
Dykstra, K.2
Krska, S.3
Vachal, P.4
Conway, D.V.5
Tudge, M.6
-
51
-
-
84938352161
-
-
Angew. Chem. 2014, 126, 4902;
-
(2014)
Angew. Chem.
, vol.126
, pp. 4902
-
-
-
53
-
-
84988473970
-
-
G.-X. Li, C. A. Morales-Rivera, Y. Wang, F. Gao, G. He, P. Liu, G. Chen, Chem. Sci. 2016, 7, 6407;
-
(2016)
Chem. Sci.
, vol.7
, pp. 6407
-
-
Li, G.-X.1
Morales-Rivera, C.A.2
Wang, Y.3
Gao, F.4
He, G.5
Liu, P.6
Chen, G.7
-
54
-
-
85021647286
-
-
J. K. Matsui, D. N. Primer, G. A. Molander, Chem. Sci. 2017, 8, 3512;
-
(2017)
Chem. Sci.
, vol.8
, pp. 3512
-
-
Matsui, J.K.1
Primer, D.N.2
Molander, G.A.3
-
55
-
-
85020677168
-
-
R. A. Garza-Sanchez, A. Tlahuext-Aca, G. Tavakoli, F. Glorius, ACS Catal. 2017, 7, 4057.
-
(2017)
ACS Catal.
, vol.7
, pp. 4057
-
-
Garza-Sanchez, R.A.1
Tlahuext-Aca, A.2
Tavakoli, G.3
Glorius, F.4
-
56
-
-
85029710114
-
-
for absorption spectra of the catalysts see the Supporting Information)
-
We believe that the use of visible-light sources minimizes absorption by the substrates and allows a mild reaction protocol with a broad functional group tolerance (for absorption spectra of the catalysts see the Supporting Information).
-
-
-
-
57
-
-
84916214381
-
-
J. J. Douglas, K. P. Cole, C. R. J. Stephenson, J. Org. Chem. 2014, 79, 11631.
-
(2014)
J. Org. Chem.
, vol.79
, pp. 11631
-
-
Douglas, J.J.1
Cole, K.P.2
Stephenson, C.R.J.3
-
58
-
-
85024927680
-
-
A. C. Edwards, A. Geist, U. Müllich, C. A. Sharrad, R. Pritchard, R. Whitehead, L. M. Harwood, Chem. Commun. 2017, 53, 8160.
-
(2017)
Chem. Commun.
, vol.53
, pp. 8160
-
-
Edwards, A.C.1
Geist, A.2
Müllich, U.3
Sharrad, C.A.4
Pritchard, R.5
Whitehead, R.6
Harwood, L.M.7
-
60
-
-
84959018638
-
-
Z. Zuo, H. Cong, W. Li, J. Choi, G. C. Fu, D. W. C. MacMillan, J. Am. Chem. Soc. 2016, 138, 1832;
-
(2016)
J. Am. Chem. Soc.
, vol.138
, pp. 1832
-
-
Zuo, Z.1
Cong, H.2
Li, W.3
Choi, J.4
Fu, G.C.5
MacMillan, D.W.C.6
-
61
-
-
85017796310
-
-
W.-M. Cheng, R. Shang, Y. Fu, ACS Catal. 2017, 7, 907.
-
(2017)
ACS Catal.
, vol.7
, pp. 907
-
-
Cheng, W.-M.1
Shang, R.2
Fu, Y.3
-
62
-
-
77954133344
-
-
L. Furst, B. S. Matsuura, J. M. R. Narayanam, J. W. Tucker, C. R. J. Stephenson, Org. Lett. 2010, 12, 3104;
-
(2010)
Org. Lett.
, vol.12
, pp. 3104
-
-
Furst, L.1
Matsuura, B.S.2
Narayanam, J.M.R.3
Tucker, J.W.4
Stephenson, C.R.J.5
-
63
-
-
84918793037
-
-
J. J. Devery III, J. J. Douglas, J. D. Nguyen, K. P. Cole, R. A. Flowers II, C. R. J. Stephenson, Chem. Sci. 2015, 6, 537;
-
(2015)
Chem. Sci.
, vol.6
, pp. 537
-
-
Devery, J.J.1
Douglas, J.J.2
Nguyen, J.D.3
Cole, K.P.4
Flowers, R.A.5
Stephenson, C.R.J.6
-
64
-
-
84959346295
-
-
E. C. Swift, T. M. Williams, C. R. J. Stephenson, Synlett 2016, 27, 754.
-
(2016)
Synlett
, vol.27
, pp. 754
-
-
Swift, E.C.1
Williams, T.M.2
Stephenson, C.R.J.3
-
65
-
-
85029695614
-
-
Minimal reaction was observed when the amino acid derived Katritzky salts were reacted with isoquinoline, presumably due to the incompatibility of electrophilic radicals with electron-deficient heteroarenes, For details, see
-
Minimal reaction was observed when the amino acid derived Katritzky salts were reacted with isoquinoline, presumably due to the incompatibility of electrophilic radicals with electron-deficient heteroarenes. For details, see:
-
-
-
-
67
-
-
0000336004
-
-
Angew. Chem. 2001, 113, 1380;
-
(2001)
Angew. Chem.
, vol.113
, pp. 1380
-
-
-
68
-
-
44449171347
-
-
F. De Vleeschouwer, V. Van Speybroeck, M. Waroquier, P. Geerlings, F. De Proft, Org. Lett. 2007, 9, 2721.
-
(2007)
Org. Lett.
, vol.9
, pp. 2721
-
-
De Vleeschouwer, F.1
Van Speybroeck, V.2
Waroquier, M.3
Geerlings, P.4
De Proft, F.5
|