-
1
-
-
80052566880
-
-
N. Kambe, T. Iwasaki, J. Terao, Chem. Soc. Rev. 2011, 40, 4937.
-
(2011)
Chem. Soc. Rev.
, vol.40
, pp. 4937
-
-
Kambe, N.1
Iwasaki, T.2
Terao, J.3
-
2
-
-
84896131010
-
-
E. Geist, A. Kirschning, T. Schmidt, Nat. Prod. Rep. 2014, 31, 441.
-
(2014)
Nat. Prod. Rep.
, vol.31
, pp. 441
-
-
Geist, E.1
Kirschning, A.2
Schmidt, T.3
-
3
-
-
84900544451
-
-
S. Z. Tasker, E. A. Standley, T. F. Jamison, Nature 2014, 509, 299;
-
(2014)
Nature
, vol.509
, pp. 299
-
-
Tasker, S.Z.1
Standley, E.A.2
Jamison, T.F.3
-
4
-
-
79952656192
-
-
R. Jana, T. P. Pathak, M. S. Sigman, Chem. Rev. 2011, 111, 1417;
-
(2011)
Chem. Rev.
, vol.111
, pp. 1417
-
-
Jana, R.1
Pathak, T.P.2
Sigman, M.S.3
-
6
-
-
72049121364
-
-
Angew. Chem. 2009, 121, 2694;
-
(2009)
Angew. Chem.
, vol.121
, pp. 2694
-
-
-
9
-
-
21244446092
-
-
Angew. Chem. 2005, 117, 680;
-
(2005)
Angew. Chem.
, vol.117
, pp. 680
-
-
-
10
-
-
84907880518
-
-
J. J. Sahn, B. A. Granger, S. F. Martin, Org. Biomol. Chem. 2014, 12, 7659.
-
(2014)
Org. Biomol. Chem.
, vol.12
, pp. 7659
-
-
Sahn, J.J.1
Granger, B.A.2
Martin, S.F.3
-
11
-
-
85043101025
-
-
Selected examples of Ni-catalyzed alkyl–alkyl cross-coupling
-
Selected examples of Ni-catalyzed alkyl–alkyl cross-coupling:
-
-
-
-
12
-
-
84865245127
-
-
P. M. Perez Garcia, T. Di Franco, A. Orsino, P. Ren, X. Hu, Org. Lett. 2012, 14, 4286;
-
(2012)
Org. Lett.
, vol.14
, pp. 4286
-
-
Perez Garcia, P.M.1
Di Franco, T.2
Orsino, A.3
Ren, P.4
Hu, X.5
-
14
-
-
84919631162
-
-
Angew. Chem. 2010, 122, 6826;
-
(2010)
Angew. Chem.
, vol.122
, pp. 6826
-
-
-
16
-
-
84940177312
-
-
Angew. Chem. 2009, 121, 2981;
-
(2009)
Angew. Chem.
, vol.121
, pp. 2981
-
-
-
20
-
-
0037165715
-
-
J. Terao, H. Watanabe, A. Ikumi, H. Kuniyasu, N. Kambe, J. Am. Chem. Soc. 2002, 124, 4222;
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 4222
-
-
Terao, J.1
Watanabe, H.2
Ikumi, A.3
Kuniyasu, H.4
Kambe, N.5
-
21
-
-
79955398877
-
-
X. Yu, T. Yang, S. Wang, H. Xu, H. Gong, Org. Lett. 2011, 13, 2138;
-
(2011)
Org. Lett.
, vol.13
, pp. 2138
-
-
Yu, X.1
Yang, T.2
Wang, S.3
Xu, H.4
Gong, H.5
-
22
-
-
84919393313
-
-
C. L. Zhao, X. Jia, X. Wang, H. G. Gong, J. Am. Chem. Soc. 2014, 136, 17645;
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 17645
-
-
Zhao, C.L.1
Jia, X.2
Wang, X.3
Gong, H.G.4
-
23
-
-
84948389324
-
-
B. Wang, Y. J. Dai, W. Q. Tong, H. G. Gong, Org. Biomol. Chem. 2015, 13, 11418;
-
(2015)
Org. Biomol. Chem.
, vol.13
, pp. 11418
-
-
Wang, B.1
Dai, Y.J.2
Tong, W.Q.3
Gong, H.G.4
-
24
-
-
84941124989
-
-
X. Lu, J. Yi, Z.-Q. Zhang, J.-J. Dai, J.-H. Liu, B. Xiao, Y. Fu, L. Liu, Chem. Eur. J. 2014, 20, 15339.
-
(2014)
Chem. Eur. J.
, vol.20
, pp. 15339
-
-
Lu, X.1
Yi, J.2
Zhang, Z.-Q.3
Dai, J.-J.4
Liu, J.-H.5
Xiao, B.6
Fu, Y.7
Liu, L.8
-
25
-
-
85043094682
-
-
Selected examples of Pd-catalyzed alkyl–alkyl cross-coupling
-
Selected examples of Pd-catalyzed alkyl–alkyl cross-coupling:
-
-
-
-
27
-
-
85007271082
-
-
J. H. Kirchhoff, C. Y. Dai, G. C. Fu, Angew. Chem. Int. Ed. 2002, 41, 1945;
-
(2002)
Angew. Chem. Int. Ed.
, vol.41
, pp. 1945
-
-
Kirchhoff, J.H.1
Dai, C.Y.2
Fu, G.C.3
-
28
-
-
0000941912
-
-
Angew. Chem. 2002, 114, 2025;
-
(2002)
Angew. Chem.
, vol.114
, pp. 2025
-
-
-
29
-
-
84960303534
-
-
X. Lu, B. Xiao, R. Shang, L. Liu, Chin. Chem. Lett. 2016, 27, 305.
-
(2016)
Chin. Chem. Lett.
, vol.27
, pp. 305
-
-
Lu, X.1
Xiao, B.2
Shang, R.3
Liu, L.4
-
30
-
-
84865430683
-
-
Selected examples of Fe-catalyzed alkyl–alkyl cross-coupling
-
Selected examples of Fe-catalyzed alkyl–alkyl cross-coupling: T. Hatakeyama, T. Hashimoto, K. K. A. D. S. Kathriarachchi, T. Zenmyo, H. Seike, M. Nakamura, Angew. Chem. Int. Ed. 2012, 51, 8834;
-
(2012)
Angew. Chem. Int. Ed.
, vol.51
, pp. 8834
-
-
Hatakeyama, T.1
Hashimoto, T.2
Kathriarachchi, K.K.A.D.S.3
Zenmyo, T.4
Seike, H.5
Nakamura, M.6
-
31
-
-
84872415608
-
-
Angew. Chem. 2012, 124, 8964.
-
(2012)
Angew. Chem.
, vol.124
, pp. 8964
-
-
-
32
-
-
85043120307
-
-
Selected examples of Cu-catalyzed alkyl–alkyl cross-coupling
-
Selected examples of Cu-catalyzed alkyl–alkyl cross-coupling:
-
-
-
-
33
-
-
84863825892
-
-
C.-T. Yang, Z.-Q. Zhang, J. Liang, J.-H. Liu, X.-Y. Lu, H.-H. Chen, L. Liu, J. Am. Chem. Soc. 2012, 134, 11124;
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 11124
-
-
Yang, C.-T.1
Zhang, Z.-Q.2
Liang, J.3
Liu, J.-H.4
Lu, X.-Y.5
Chen, H.-H.6
Liu, L.7
-
34
-
-
84865838299
-
-
P. Ren, L.-A. Stern, X. Hu, Angew. Chem. Int. Ed. 2012, 51, 9110;
-
(2012)
Angew. Chem. Int. Ed.
, vol.51
, pp. 9110
-
-
Ren, P.1
Stern, L.-A.2
Hu, X.3
-
35
-
-
84944725081
-
-
Angew. Chem. 2012, 124, 9244;
-
(2012)
Angew. Chem.
, vol.124
, pp. 9244
-
-
-
36
-
-
79954593181
-
-
C.-T. Yang, Z.-Q. Zhang, Y.-C. Liu, L. Liu, Angew. Chem. Int. Ed. 2011, 50, 3904;
-
(2011)
Angew. Chem. Int. Ed.
, vol.50
, pp. 3904
-
-
Yang, C.-T.1
Zhang, Z.-Q.2
Liu, Y.-C.3
Liu, L.4
-
37
-
-
84855434545
-
-
Angew. Chem. 2011, 123, 3990;
-
(2011)
Angew. Chem.
, vol.123
, pp. 3990
-
-
-
38
-
-
34250863375
-
-
J. Terao, H. Todo, S. A. Begum, H. Kuniyasu, N. Kambe, Angew. Chem. Int. Ed. 2007, 46, 2086;
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 2086
-
-
Terao, J.1
Todo, H.2
Begum, S.A.3
Kuniyasu, H.4
Kambe, N.5
-
39
-
-
84938204281
-
-
Angew. Chem. 2007, 119, 2132;
-
(2007)
Angew. Chem.
, vol.119
, pp. 2132
-
-
-
40
-
-
84928652729
-
-
S. Thapa, B. Shrestha, S. K. Gurung, R. Giri, Org. Biomol. Chem. 2015, 13, 4816;
-
(2015)
Org. Biomol. Chem.
, vol.13
, pp. 4816
-
-
Thapa, S.1
Shrestha, B.2
Gurung, S.K.3
Giri, R.4
-
41
-
-
84941091154
-
-
J.-H. Liu, C.-T. Yang, X.-Y. Lu, Z.-Q. Zhang, L. Xu, M. Cui, X. Lu, B. Xiao, Y. Fu, L. Liu, Chem. Eur. J. 2014, 20, 15334.
-
(2014)
Chem. Eur. J.
, vol.20
, pp. 15334
-
-
Liu, J.-H.1
Yang, C.-T.2
Lu, X.-Y.3
Zhang, Z.-Q.4
Xu, L.5
Cui, M.6
Lu, X.7
Xiao, B.8
Fu, Y.9
Liu, L.10
-
42
-
-
84879744985
-
-
Selected examples of Co-catalyzed alkyl–alkyl cross-coupling
-
Selected examples of Co-catalyzed alkyl–alkyl cross-coupling: T. Iwasaki, H. Takagawa, S. P. Singh, H. Kuniyasu, N. Kambe, J. Am. Chem. Soc. 2013, 135, 9604.
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 9604
-
-
Iwasaki, T.1
Takagawa, H.2
Singh, S.P.3
Kuniyasu, H.4
Kambe, N.5
-
44
-
-
84979646147
-
-
Angew. Chem. 2016, 128, 2682;
-
(2016)
Angew. Chem.
, vol.128
, pp. 2682
-
-
-
45
-
-
84922792786
-
-
J. C. Lo, J. Gui, Y. Yabe, C. M. Pan, P. S. Baran, Nature 2014, 516, 343;
-
(2014)
Nature
, vol.516
, pp. 343
-
-
Lo, J.C.1
Gui, J.2
Yabe, Y.3
Pan, C.M.4
Baran, P.S.5
-
46
-
-
84898962630
-
-
T.-S. Mei, H. H. Patel, M. S. Sigman, Nature 2014, 508, 340.
-
(2014)
Nature
, vol.508
, pp. 340
-
-
Mei, T.-S.1
Patel, H.H.2
Sigman, M.S.3
-
47
-
-
84916887444
-
-
C. Shen, P. Zhang, Q. Sun, S. Bai, T. S. A. Hor, X. Liu, Chem. Soc. Rev. 2015, 44, 291;
-
(2015)
Chem. Soc. Rev.
, vol.44
, pp. 291
-
-
Shen, C.1
Zhang, P.2
Sun, Q.3
Bai, S.4
Hor, T.S.A.5
Liu, X.6
-
49
-
-
84864437112
-
-
W. I. Dzik, P. P. Lange, L. J. Goossen, Chem. Sci. 2012, 3, 2671;
-
(2012)
Chem. Sci.
, vol.3
, pp. 2671
-
-
Dzik, W.I.1
Lange, P.P.2
Goossen, L.J.3
-
53
-
-
84901624865
-
-
Z. Li, J. Chen, W. Su, M. Hong, Acta Chim. Sinica 2014, 72, 552.
-
(2014)
Acta Chim. Sinica
, vol.72
, pp. 552
-
-
Li, Z.1
Chen, J.2
Su, W.3
Hong, M.4
-
54
-
-
84863527168
-
-
R. J. Phipps, L. McMurray, S. Ritter, H. A. Duong, M. J. Gaunt, J. Am. Chem. Soc. 2012, 134, 10773;
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 10773
-
-
Phipps, R.J.1
McMurray, L.2
Ritter, S.3
Duong, H.A.4
Gaunt, M.J.5
-
56
-
-
0000772024
-
-
Angew. Chem. 1983, 95, 771.
-
(1983)
Angew. Chem.
, vol.95
, pp. 771
-
-
-
57
-
-
84962916539
-
-
X. Lu, B. Xiao, Z. Zhang, T. Gong, W. Su, Y. Fu, L. Liu, Nat. Commun. 2016, 7, 11129.
-
(2016)
Nat. Commun.
, vol.7
, pp. 11129
-
-
Lu, X.1
Xiao, B.2
Zhang, Z.3
Gong, T.4
Su, W.5
Fu, Y.6
Liu, L.7
-
58
-
-
85043113919
-
-
Recent reviews for light-induced decarboxylative coupling reactions
-
Recent reviews for light-induced decarboxylative coupling reactions:
-
-
-
-
59
-
-
84955214922
-
-
J. Xuan, Z.-G. Zhang, W.-J. Xiao, Angew. Chem. Int. Ed. 2015, 54, 15632;
-
(2015)
Angew. Chem. Int. Ed.
, vol.54
, pp. 15632
-
-
Xuan, J.1
Zhang, Z.-G.2
Xiao, W.-J.3
-
60
-
-
84973119747
-
-
Angew. Chem. 2015, 127, 15854;
-
(2015)
Angew. Chem.
, vol.127
, pp. 15854
-
-
-
61
-
-
84880124916
-
-
C. K. Prier, D. A. Rankic, D. W. C. MacMillan, Chem. Rev. 2013, 113, 5322;
-
(2013)
Chem. Rev.
, vol.113
, pp. 5322
-
-
Prier, C.K.1
Rankic, D.A.2
MacMillan, D.W.C.3
-
62
-
-
84897915531
-
-
M. N. Hopkinson, B. Sahoo, J.-L. Li, F. Glorius, Chem. Eur. J. 2014, 20, 3874.
-
(2014)
Chem. Eur. J.
, vol.20
, pp. 3874
-
-
Hopkinson, M.N.1
Sahoo, B.2
Li, J.-L.3
Glorius, F.4
-
63
-
-
84959450281
-
-
During the preparation of our work, Baran and co-workers reported Ni-catalyzed decarboxylative cross-coupling of aliphatic carboxylic acids, which employs NHPI esters and aryl zinc reagents
-
During the preparation of our work, Baran and co-workers reported Ni-catalyzed decarboxylative cross-coupling of aliphatic carboxylic acids, which employs NHPI esters and aryl zinc reagents: J. Cornella, J. T. Edwards, T. Qin, S. Kawamura, J. Wang, C.-M. Pan, R. Gianatassio, M. Schmidt, M. D. Eastgate, P. S. Baran, J. Am. Chem. Soc. 2016, 138, 2174.
-
(2016)
J. Am. Chem. Soc.
, vol.138
, pp. 2174
-
-
Cornella, J.1
Edwards, J.T.2
Qin, T.3
Kawamura, S.4
Wang, J.5
Pan, C.-M.6
Gianatassio, R.7
Schmidt, M.8
Eastgate, M.D.9
Baran, P.S.10
-
65
-
-
81355154663
-
-
X. Hu, Chem. Sci. 2011, 2, 1867;
-
(2011)
Chem. Sci.
, vol.2
, pp. 1867
-
-
Hu, X.1
-
66
-
-
84962421759
-
-
Z. Li, Y.-Y. Jiang, Y. Fu, Chem. Eur. J. 2012, 18, 4345;
-
(2012)
Chem. Eur. J.
, vol.18
, pp. 4345
-
-
Li, Z.1
Jiang, Y.-Y.2
Fu, Y.3
-
67
-
-
3042734823
-
-
T. J. Anderson, G. D. Jones, D. A. Vicic, J. Am. Chem. Soc. 2004, 126, 8100;
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 8100
-
-
Anderson, T.J.1
Jones, G.D.2
Vicic, D.A.3
-
69
-
-
84882289438
-
-
J. Breitenfeld, J. Ruiz, M. D. Wodrich, X. Hu, J. Am. Chem. Soc. 2013, 135, 12004;
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 12004
-
-
Breitenfeld, J.1
Ruiz, J.2
Wodrich, M.D.3
Hu, X.4
-
70
-
-
84905870618
-
-
H. H. Ke, X. F. Chen, Y. Y. Feng, G. Zou, Sci. China Chem. 2014, 57, 1126;
-
(2014)
Sci. China Chem.
, vol.57
, pp. 1126
-
-
Ke, H.H.1
Chen, X.F.2
Feng, Y.Y.3
Zou, G.4
-
71
-
-
84935077256
-
-
Y. Xiao, Q. Pan, X. Zhang, Acta Chim. Sinica 2015, 73, 383;
-
(2015)
Acta Chim. Sinica
, vol.73
, pp. 383
-
-
Xiao, Y.1
Pan, Q.2
Zhang, X.3
|