-
1
-
-
85017989352
-
-
Eds., Wiley-VCH, Weinheim
-
Metal-Catalyzed Cross-Coupling Reactions and More (Eds.: A. de Meijere, S. Bräse, M. Oestreich), Wiley-VCH, Weinheim, 2014;
-
(2014)
Metal-Catalyzed Cross-Coupling Reactions and More
-
-
de Meijere, A.1
Bräse, S.2
Oestreich, M.3
-
3
-
-
84881498225
-
-
Ed., Springer, Berlin, Heidelberg
-
Applied Cross-Coupling Reactions (Lecture Notes in Chemistry), Vol. 80 (Ed.: Y. Nishihara), Springer, Berlin, Heidelberg, 2013.
-
(2013)
Applied Cross-Coupling Reactions (Lecture Notes in Chemistry), Vol. 80
-
-
Nishihara, Y.1
-
4
-
-
85043821182
-
-
For selected general reviews on photoredox catalysis, see
-
For selected general reviews on photoredox catalysis, see:
-
-
-
-
6
-
-
77957351024
-
-
Angew. Chem. 2009, 121, 9969–9974;
-
(2009)
Angew. Chem.
, vol.121
, pp. 9969-9974
-
-
-
7
-
-
77953990194
-
-
T. P. Yoon, M. A. Ischay, J. Du, Nat. Chem. 2010, 2, 527–532;
-
(2010)
Nat. Chem.
, vol.2
, pp. 527-532
-
-
Yoon, T.P.1
Ischay, M.A.2
Du, J.3
-
11
-
-
84866379128
-
-
Angew. Chem. 2012, 124, 6934–6944;
-
(2012)
Angew. Chem.
, vol.124
, pp. 6934-6944
-
-
-
14
-
-
84880124916
-
-
C. K. Prier, D. A. Rankic, D. W. C. MacMillan, Chem. Rev. 2013, 113, 5322–5363;
-
(2013)
Chem. Rev.
, vol.113
, pp. 5322-5363
-
-
Prier, C.K.1
Rankic, D.A.2
MacMillan, D.W.C.3
-
16
-
-
84955214922
-
-
J. Xuan, Z.-G. Zhang, W.-J. Xiao, Angew. Chem. Int. Ed. 2015, 54, 15632–15641;
-
(2015)
Angew. Chem. Int. Ed.
, vol.54
, pp. 15632-15641
-
-
Xuan, J.1
Zhang, Z.-G.2
Xiao, W.-J.3
-
17
-
-
84973119747
-
-
Angew. Chem. 2015, 127, 15854–15864.
-
(2015)
Angew. Chem.
, vol.127
, pp. 15854-15864
-
-
-
19
-
-
84897915531
-
-
M. N. Hopkinson, B. Sahoo, J.-L. Li, F. Glorius, Chem. Eur. J. 2014, 20, 3874–3886;
-
(2014)
Chem. Eur. J.
, vol.20
, pp. 3874-3886
-
-
Hopkinson, M.N.1
Sahoo, B.2
Li, J.-L.3
Glorius, F.4
-
22
-
-
85043797430
-
-
For initial work in the field of photoredox/nickel dual catalysis, see
-
For initial work in the field of photoredox/nickel dual catalysis, see:
-
-
-
-
23
-
-
84904800842
-
-
J. C. Tellis, D. N. Primer, G. A. Molander, Science 2014, 345, 433–436;
-
(2014)
Science
, vol.345
, pp. 433-436
-
-
Tellis, J.C.1
Primer, D.N.2
Molander, G.A.3
-
24
-
-
84904797499
-
-
Z. Zuo, D. T. Ahneman, L. Chu, J. A. Terrett, A. G. Doyle, D. W. C. MacMillan, Science 2014, 345, 437–440.
-
(2014)
Science
, vol.345
, pp. 437-440
-
-
Zuo, Z.1
Ahneman, D.T.2
Chu, L.3
Terrett, J.A.4
Doyle, A.G.5
MacMillan, D.W.C.6
-
25
-
-
85043807967
-
-
For selected recent reports on photoredox/nickel dual catalysis, see
-
For selected recent reports on photoredox/nickel dual catalysis, see:
-
-
-
-
26
-
-
84965013481
-
-
M. H. Shaw, V. W. Shurtleff, J. A. Terrett, J. D. Cuthbertson, D. W. C. MacMillan, Science 2016, 352, 1304–1308;
-
(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
-
27
-
-
84959018638
-
-
Z. Zuo, H. Cong, W. Li, J. Choi, G. C. Fu, D. W. C. MacMillan, J. Am. Chem. Soc. 2016, 138, 1832–1835;
-
(2016)
J. Am. Chem. Soc.
, vol.138
, pp. 1832-1835
-
-
Zuo, Z.1
Cong, H.2
Li, W.3
Choi, J.4
Fu, G.C.5
MacMillan, D.W.C.6
-
28
-
-
84978932764
-
-
P. Zhang, C. C. Le, D. W. C. MacMillan, J. Am. Chem. Soc. 2016, 138, 8084–8087;
-
(2016)
J. Am. Chem. Soc.
, vol.138
, pp. 8084-8087
-
-
Zhang, P.1
Le, C.C.2
MacMillan, D.W.C.3
-
29
-
-
84939839315
-
-
J. A. Terrett, J. D. Cuthbertson, V. W. Shurtleff, D. W. C. MacMillan, Nature 2015, 524, 330–334;
-
(2015)
Nature
, vol.524
, pp. 330-334
-
-
Terrett, J.A.1
Cuthbertson, J.D.2
Shurtleff, V.W.3
MacMillan, D.W.C.4
-
30
-
-
84921483701
-
-
A. Noble, S. J. McCarver, D. W. C. MacMillan, J. Am. Chem. Soc. 2015, 137, 624–627;
-
(2015)
J. Am. Chem. Soc.
, vol.137
, pp. 624-627
-
-
Noble, A.1
McCarver, S.J.2
MacMillan, D.W.C.3
-
32
-
-
84930268175
-
-
L. Chu, J. M. Lipshultz, D. W. C. MacMillan, Angew. Chem. Int. Ed. 2015, 54, 7929–7933;
-
(2015)
Angew. Chem. Int. Ed.
, vol.54
, pp. 7929-7933
-
-
Chu, L.1
Lipshultz, J.M.2
MacMillan, D.W.C.3
-
33
-
-
84940893637
-
-
Angew. Chem. 2015, 127, 8040–8044;
-
(2015)
Angew. Chem.
, vol.127
, pp. 8040-8044
-
-
-
34
-
-
84975229840
-
-
J. C. Tellis, J. Amani, G. A. Molander, Org. Lett. 2016, 18, 2994–2997;
-
(2016)
Org. Lett.
, vol.18
, pp. 2994-2997
-
-
Tellis, J.C.1
Amani, J.2
Molander, G.A.3
-
35
-
-
84973444466
-
-
R. Karimi-Nami, J. C. Tellis, G. A. Molander, Org. Lett. 2016, 18, 2572–2575;
-
(2016)
Org. Lett.
, vol.18
, pp. 2572-2575
-
-
Karimi-Nami, R.1
Tellis, J.C.2
Molander, G.A.3
-
36
-
-
84963851481
-
-
M. Jouffroy, G. H. M. Davies, G. A. Molander, Org. Lett. 2016, 18, 1606–1609;
-
(2016)
Org. Lett.
, vol.18
, pp. 1606-1609
-
-
Jouffroy, M.1
Davies, G.H.M.2
Molander, G.A.3
-
37
-
-
84955181954
-
-
M. El Khatib, R. A. M. Serafim, G. A. Molander, Angew. Chem. Int. Ed. 2016, 55, 254–258;
-
(2016)
Angew. Chem. Int. Ed.
, vol.55
, pp. 254-258
-
-
El Khatib, M.1
Serafim, R.A.M.2
Molander, G.A.3
-
38
-
-
84962213962
-
-
Angew. Chem. 2016, 128, 262–266;
-
(2016)
Angew. Chem.
, vol.128
, pp. 262-266
-
-
-
39
-
-
84959020578
-
-
J. Amani, E. Sodagar, G. A. Molander, Org. Lett. 2016, 18, 732–735;
-
(2016)
Org. Lett.
, vol.18
, pp. 732-735
-
-
Amani, J.1
Sodagar, E.2
Molander, G.A.3
-
40
-
-
84923260920
-
-
D. N. Primer, I. Karakaya, J. C. Tellis, G. A. Molander, J. Am. Chem. Soc. 2015, 137, 2195–2198;
-
(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
-
41
-
-
84935125121
-
-
I. Karakaya, D. N. Primer, G. A. Molander, Org. Lett. 2015, 17, 3294–3297;
-
(2015)
Org. Lett.
, vol.17
, pp. 3294-3297
-
-
Karakaya, I.1
Primer, D.N.2
Molander, G.A.3
-
42
-
-
84928492420
-
-
O. Gutierrez, J. C. Tellis, D. N. Primer, G. A. Molander, M. C. Kozlowski, J. Am. Chem. Soc. 2015, 137, 4896–4899;
-
(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
-
44
-
-
84943457879
-
-
V. Corcé, L.-M. Chamoreau, E. Derat, J.-P. Goddard, C. Ollivier, L. Fensterbank, Angew. Chem. Int. Ed. 2015, 54, 11414–11418;
-
(2015)
Angew. Chem. Int. Ed.
, vol.54
, pp. 11414-11418
-
-
Corcé, V.1
Chamoreau, L.-M.2
Derat, E.3
Goddard, J.-P.4
Ollivier, C.5
Fensterbank, L.6
-
45
-
-
84994050414
-
-
Angew. Chem. 2015, 127, 11576–11580;
-
(2015)
Angew. Chem.
, vol.127
, pp. 11576-11580
-
-
-
46
-
-
84959010717
-
-
M. S. Oderinde, M. Frenette, D. W. Robbins, B. Aquila, J. W. Johannes, J. Am. Chem. Soc. 2016, 138, 1760–1763;
-
(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.W.5
-
48
-
-
84993989389
-
-
Angew. Chem. 2016, 128, 4108–4111.
-
(2016)
Angew. Chem.
, vol.128
, pp. 4108-4111
-
-
-
49
-
-
85043831884
-
-
For selected reports using aryl and vinyl halides, see
-
For selected reports using aryl and vinyl halides, see:
-
-
-
-
50
-
-
84959018709
-
-
N. R. Patel, C. B. Kelly, M. Jouffroy, G. A. Molander, Org. Lett. 2016, 18, 764–767;
-
(2016)
Org. Lett.
, vol.18
, pp. 764-767
-
-
Patel, N.R.1
Kelly, C.B.2
Jouffroy, M.3
Molander, G.A.4
-
51
-
-
84955312797
-
-
M. Jouffroy, D. N. Primer, G. A. Molander, J. Am. Chem. Soc. 2016, 138, 475–478;
-
(2016)
J. Am. Chem. Soc.
, vol.138
, pp. 475-478
-
-
Jouffroy, M.1
Primer, D.N.2
Molander, G.A.3
-
52
-
-
84954383075
-
-
D. Ryu, D. N. Primer, J. C. Tellis, G. A. Molander, Chem. Eur. J. 2016, 22, 120–123.
-
(2016)
Chem. Eur. J.
, vol.22
, pp. 120-123
-
-
Ryu, D.1
Primer, D.N.2
Tellis, J.C.3
Molander, G.A.4
-
53
-
-
85043833898
-
-
For reviews on the use of C−O electrophiles, see
-
For reviews on the use of C−O electrophiles, see:
-
-
-
-
54
-
-
78650506132
-
-
D. G. Yu, B. J. Li, Z. J. Shi, Acc. Chem. Res. 2010, 43, 1486–1495;
-
(2010)
Acc. Chem. Res.
, vol.43
, pp. 1486-1495
-
-
Yu, D.G.1
Li, B.J.2
Shi, Z.J.3
-
55
-
-
79551474698
-
-
B. J. Li, D. G. Yu, C. L. Sun, Z. J. Shi, Chem. Eur. J. 2011, 17, 1728–1759;
-
(2011)
Chem. Eur. J.
, vol.17
, pp. 1728-1759
-
-
Li, B.J.1
Yu, D.G.2
Sun, C.L.3
Shi, Z.J.4
-
56
-
-
79952145052
-
-
B. M. Rosen, K. W. Quasdorf, D. A. Wilson, N. Zhang, A. M. Resmerita, N. K. Garg, V. Percec, Chem. Rev. 2011, 111, 1346–1416;
-
(2011)
Chem. Rev.
, vol.111
, pp. 1346-1416
-
-
Rosen, B.M.1
Quasdorf, K.W.2
Wilson, D.A.3
Zhang, N.4
Resmerita, A.M.5
Garg, N.K.6
Percec, V.7
-
59
-
-
84873930619
-
-
S. I. Kozhushkov, H. K. Potukuchiw, L. Ackermann, Catal. Sci. Technol. 2013, 3, 562–571;
-
(2013)
Catal. Sci. Technol.
, vol.3
, pp. 562-571
-
-
Kozhushkov, S.I.1
Potukuchiw, H.K.2
Ackermann, L.3
-
60
-
-
84908538286
-
-
J. Cornella, C. Zarate, R. Martin, Chem. Soc. Rev. 2014, 43, 8081–8097;
-
(2014)
Chem. Soc. Rev.
, vol.43
, pp. 8081-8097
-
-
Cornella, J.1
Zarate, C.2
Martin, R.3
-
62
-
-
85043804724
-
-
For selected recent reviews on Ni-catalyzed reactions, see
-
For selected recent reviews on Ni-catalyzed reactions, see:
-
-
-
-
67
-
-
84900544451
-
-
S. Z. Tasker, E. A. Standley, T. F. Jamison, Nature 2014, 509, 299–309.
-
(2014)
Nature
, vol.509
, pp. 299-309
-
-
Tasker, S.Z.1
Standley, E.A.2
Jamison, T.F.3
-
68
-
-
84941044565
-
-
M. Leiendecker, C.-C. Hsiao, L. Guo, N. Alandini, M. Rueping, Angew. Chem. Int. Ed. 2014, 53, 12912–12915;
-
(2014)
Angew. Chem. Int. Ed.
, vol.53
, pp. 12912-12915
-
-
Leiendecker, M.1
Hsiao, C.-C.2
Guo, L.3
Alandini, N.4
Rueping, M.5
-
69
-
-
84954402539
-
-
Angew. Chem. 2014, 126, 13126–13129;
-
(2014)
Angew. Chem.
, vol.126
, pp. 13126-13129
-
-
-
70
-
-
84940973368
-
-
M. Leiendecker, A. Chatupheeraphat, M. Rueping, Org. Chem. Front. 2015, 2, 350–353;
-
(2015)
Org. Chem. Front.
, vol.2
, pp. 350-353
-
-
Leiendecker, M.1
Chatupheeraphat, A.2
Rueping, M.3
-
71
-
-
84921690402
-
-
L. Guo, M. Leiendecker, C.-C. Hsiao, C. Baumann, M. Rueping, Chem. Commun. 2015, 51, 1937–1940;
-
(2015)
Chem. Commun.
, vol.51
, pp. 1937-1940
-
-
Guo, L.1
Leiendecker, M.2
Hsiao, C.-C.3
Baumann, C.4
Rueping, M.5
-
72
-
-
84981765530
-
-
X. Liu, C.-C. Hsiao, I. Kalvet, M. Leiendecker, L. Guo, F. Schoenebeck, M. Rueping, Angew. Chem. Int. Ed. 2016, 55, 6093–6098;
-
(2016)
Angew. Chem. Int. Ed.
, vol.55
, pp. 6093-6098
-
-
Liu, X.1
Hsiao, C.-C.2
Kalvet, I.3
Leiendecker, M.4
Guo, L.5
Schoenebeck, F.6
Rueping, M.7
-
73
-
-
84981272516
-
-
Angew. Chem. 2016, 128, 6198–6203;
-
(2016)
Angew. Chem.
, vol.128
, pp. 6198-6203
-
-
-
74
-
-
84977134279
-
-
L. Guo, C.-C. Hsiao, H. Yue, X. Liu, M. Rueping, ACS Catal. 2016, 6, 4438–4442;
-
(2016)
ACS Catal.
, vol.6
, pp. 4438-4442
-
-
Guo, L.1
Hsiao, C.-C.2
Yue, H.3
Liu, X.4
Rueping, M.5
-
75
-
-
84979723089
-
-
L. Guo, A. Chatupheeraphat, M. Rueping, Angew. Chem. Int. Ed. 2016, 55, 7403–7407;
-
(2016)
Angew. Chem. Int. Ed.
, vol.55
, pp. 7403-7407
-
-
Guo, L.1
Chatupheeraphat, A.2
Rueping, M.3
-
76
-
-
84993947448
-
-
Angew. Chem. 2016, 128, 7529–7533.
-
(2016)
Angew. Chem.
, vol.128
, pp. 7529-7533
-
-
-
77
-
-
85043811552
-
-
For an early example of a photoredox catalyzed decarboxylation, see
-
For an early example of a photoredox catalyzed decarboxylation, see:
-
-
-
-
78
-
-
84882434156
-
-
references cited therein; for a recent example from our group, see
-
L. Chen, C. S. Chao, Y. Pan, S. Dong, Y. C. Teo, J. Wang, C.-H. Tan, Org. Biomol. Chem. 2013, 11, 5922–5925, and references cited therein; for a recent example from our group, see:
-
(2013)
Org. Biomol. Chem.
, vol.11
, pp. 5922-5925
-
-
Chen, L.1
Chao, C.S.2
Pan, Y.3
Dong, S.4
Teo, Y.C.5
Wang, J.6
Tan, C.-H.7
-
79
-
-
84985997763
-
-
A. Millet, Q. Lefebvre, M. Rueping, Chem. Eur. J. 2016, 22, 13464–13468.
-
(2016)
Chem. Eur. J.
, vol.22
, pp. 13464-13468
-
-
Millet, A.1
Lefebvre, Q.2
Rueping, M.3
-
80
-
-
84983301353
-
Duing the publication process the use of aryltriflates with alkylsilicates has been published
-
Duing the publication process the use of aryltriflates with alkylsilicates has been published: N. R. Patel, G. A. Molander, J. Org. Chem. 2016, 81, 7271–7275.
-
(2016)
J. Org. Chem.
, vol.81
, pp. 7271-7275
-
-
Patel, N.R.1
Molander, G.A.2
|