-
1
-
-
79952178016
-
-
For selected reviews on Pd-catalysed Suzuki-Miyaura reactions, see
-
For selected reviews on Pd-catalysed Suzuki-Miyaura reactions, see
-
-
-
-
5
-
-
0037175592
-
-
S. Kotha, K. Lahiri, D. Kashinath, Tetrahedron 2002, 58, 9633-9695.
-
(2002)
Tetrahedron
, vol.58
, pp. 9633-9695
-
-
Kotha, S.1
Lahiri, K.2
Kashinath, D.3
-
7
-
-
7644241634
-
-
F. Bellina, A. Carpita, R. Rossi, Synthesis 2004, 15, 2419-2440.
-
(2004)
Synthesis
, vol.15
, pp. 2419-2440
-
-
Bellina, F.1
Carpita, A.2
Rossi, R.3
-
9
-
-
33746055935
-
-
V. Percec, J.-Y. Bae, D. H. Hill, J. Org. Chem. 1995, 60, 1060-1065.
-
(1995)
J. Org. Chem.
, vol.60
, pp. 1060-1065
-
-
Percec, V.1
Bae, J.-Y.2
Hill, D.H.3
-
10
-
-
79952179949
-
-
For Ni-catalysed Suzuki-Miyaura aryl-aryl coupling reactions of haloarenes using the chloride, see
-
For Ni-catalysed Suzuki-Miyaura aryl-aryl coupling reactions of haloarenes using the chloride, see
-
-
-
-
11
-
-
0029878151
-
-
S. Saito, M. Sakai, N. Miyaura, Tetrahedron Lett. 1996, 37, 2993-2996.
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 2993-2996
-
-
Saito, S.1
Sakai, M.2
Miyaura, N.3
-
13
-
-
0000728442
-
-
S. Saito, S. Oh-tani, N. Miyaura, J. Org. Chem. 1997, 62, 8024-8030.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 8024-8030
-
-
Saito, S.1
Oh-Tani, S.2
Miyaura, N.3
-
14
-
-
0033583136
-
-
J.-C. Galland, M. Savignac, J.-P. Genêt, Tetrahedron Lett. 1999, 40, 2323-2326.
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 2323-2326
-
-
Galland, J.-C.1
Savignac, M.2
Genêt, J.-P.3
-
17
-
-
34848920071
-
-
using the bromide/iodide, see
-
L. Zhou, Q. Miao, R. He, X. Feng, M. Bao, Tetrahedron Lett. 2007, 48, 7899-7902, using the bromide/iodide, see
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 7899-7902
-
-
Zhou, L.1
Miao, Q.2
He, R.3
Feng, X.4
Bao, M.5
-
21
-
-
79952148569
-
-
For Ni-catalysed Suzuki-Miyaura aryl-aryl coupling reactions of aryl sulfonates (OTs, OBs, OMs), see
-
For Ni-catalysed Suzuki-Miyaura aryl-aryl coupling reactions of aryl sulfonates (OTs, OBs, OMs), see
-
-
-
-
22
-
-
0000894049
-
-
D. Zim, V. R. Lando, J. Dupont, A. L. Monterio, Org. Lett. 2001, 3, 3049-3051.
-
(2001)
Org. Lett.
, vol.3
, pp. 3049-3051
-
-
Zim, D.1
Lando, V.R.2
Dupont, J.3
Monterio, A.L.4
-
23
-
-
2442441967
-
-
V. Percec, G. M. Golding, J. Smidrkal, O. Weichold, J. Org. Chem. 2004, 69, 3447-3452.
-
(2004)
J. Org. Chem.
, vol.69
, pp. 3447-3452
-
-
Percec, V.1
Golding, G.M.2
Smidrkal, J.3
Weichold, O.4
-
24
-
-
66149146577
-
-
J. Kuroda, K. Inamoto, K. Hiroya, T. Doi, Eur. J. Org. Chem. 2009, 2251-2261.
-
(2009)
Eur. J. Org. Chem.
, pp. 2251-2261
-
-
Kuroda, J.1
Inamoto, K.2
Hiroya, K.3
Doi, T.4
-
26
-
-
79952133125
-
-
For Ni-catalysed Suzuki-Miyaura aryl-aryl coupling reactions of other electrophiles containing unusual leaving groups using aryl carboxylates, see
-
For Ni-catalysed Suzuki-Miyaura aryl-aryl coupling reactions of other electrophiles containing unusual leaving groups using aryl carboxylates, see
-
-
-
-
27
-
-
55549111900
-
-
B.-T. Guan, Y. Wang, B.-J. Li, D.-G. Yu, Z.-J. Shi, J. Am. Chem. Soc. 2008, 130, 14468-14470.
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 14468-14470
-
-
Guan, B.-T.1
Wang, Y.2
Li, B.-J.3
Yu, D.-G.4
Shi, Z.-J.5
-
28
-
-
55549084571
-
-
using aryl carbamates, see
-
K. W. Quasdorf, X. Tian, N. K. Garg, J. Am. Chem. Soc. 2008, 130, 14422-14423, using aryl carbamates, see
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 14422-14423
-
-
Quasdorf, K.W.1
Tian, X.2
Garg, N.K.3
-
29
-
-
71749085673
-
-
K. W. Quasdorf, M. Riener, K. V. Petrova, N. K. Garg, J. Am. Chem. Soc. 2009, 131, 17748-17749.
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 17748-17749
-
-
Quasdorf, K.W.1
Riener, M.2
Petrova, K.V.3
Garg, N.K.4
-
30
-
-
71749088399
-
-
A. Antoft-Finch, T. Blackburn, V. Snieckus, J. Am. Chem. Soc. 2009, 131, 17750-17752.
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 17750-17752
-
-
Antoft-Finch, A.1
Blackburn, T.2
Snieckus, V.3
-
31
-
-
76849090306
-
-
L. Xu, B.-J. Li, Z.-H. Wu, X.-Y. Lu, B.-T. Guan, B.-Q. Wang, K.-Q. Zhao, Z.-J. Shi, Org. Lett. 2010, 12, 884-887.
-
(2010)
Org. Lett.
, vol.12
, pp. 884-887
-
-
Xu, L.1
Li, B.-J.2
Wu, Z.-H.3
Lu, X.-Y.4
Guan, B.-T.5
Wang, B.-Q.6
Zhao, K.-Q.7
Shi, Z.-J.8
-
32
-
-
76249106717
-
-
L. J. Gooßen, K. Gooßen, C. Stanciu, Angew. Chem. 2009, 121, 3621
-
(2009)
Angew. Chem.
, vol.121
, pp. 3621
-
-
Gooßen, L.J.1
Gooßen, K.2
Stanciu, C.3
-
33
-
-
70349970582
-
-
using aryl methyl ether, see
-
Angew. Chem. Int. Ed. 2009, 48, 3569-3571, using aryl methyl ether, see
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 3569-3571
-
-
-
34
-
-
57749094839
-
-
M. Tobisu, T. Shimasaki, N. Chatani, Angew. Chem. 2008, 120, 4944
-
(2008)
Angew. Chem.
, vol.120
, pp. 4944
-
-
Tobisu, M.1
Shimasaki, T.2
Chatani, N.3
-
35
-
-
50049090202
-
-
using aryl nitriles, see
-
Angew. Chem. Int. Ed. 2008, 47, 4866-4869, using aryl nitriles, see
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 4866-4869
-
-
-
36
-
-
68149110231
-
-
using aryltrimethylammonium salts, see
-
D.-G. Yu, M. Yu, B.-T. Guan, B.-J. Li, Y. Zheng, Z.-H. Wu, Z.-J. Shi, Org. Lett. 2009, 11, 3374-3377, using aryltrimethylammonium salts, see
-
(2009)
Org. Lett.
, vol.11
, pp. 3374-3377
-
-
Yu, D.-G.1
Yu, M.2
Guan, B.-T.3
Li, B.-J.4
Zheng, Y.5
Wu, Z.-H.6
Shi, Z.-J.7
-
37
-
-
0038627682
-
-
using aryl sulfamates, see
-
S. B. Blakey, D. W. C. MacMillan, J. Am. Chem. Soc. 2003, 125, 6046-6047., using aryl sulfamates, see
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 6046-6047
-
-
Blakey, S.B.1
MacMillan, D.W.C.2
-
40
-
-
79952130054
-
-
For selected Ni heterogeneously catalysed Suzuki-Miyaura aryl-aryl coupling reactions, see
-
For selected Ni heterogeneously catalysed Suzuki-Miyaura aryl-aryl coupling reactions, see
-
-
-
-
41
-
-
0034616375
-
-
B. H. Lipshutz, J. A. Sclafani, P. A. Blomgren, Tetrahedron 2000, 56, 2139-2144.
-
(2000)
Tetrahedron
, vol.56
, pp. 2139-2144
-
-
Lipshutz, B.H.1
Sclafani, J.A.2
Blomgren, P.A.3
-
42
-
-
43549125514
-
-
B. H. Lipshutz, T. Butler, E. Swift, Org. Lett. 2008, 10, 697-700.
-
(2008)
Org. Lett.
, vol.10
, pp. 697-700
-
-
Lipshutz, B.H.1
Butler, T.2
Swift, E.3
-
43
-
-
79952136053
-
-
For room-temperature Suzuki-Miyaura aryl-aryl coupling reactions catalysed by nickel catalysts, see
-
For room-temperature Suzuki-Miyaura aryl-aryl coupling reactions catalysed by nickel catalysts, see
-
-
-
-
46
-
-
33644845071
-
-
Z.-Y. Tang, S. Spinella, Q.-S. Hu, Tetrahedron Lett. 2006, 47, 2427-2430.
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 2427-2430
-
-
Tang, Z.-Y.1
Spinella, S.2
Hu, Q.-S.3
-
48
-
-
60949111149
-
-
D. A. Wilson, C. J. Wilson, B. M. Rosen, V. Percec, Org. Lett. 2008, 10, 4879-4882.
-
(2008)
Org. Lett.
, vol.10
, pp. 4879-4882
-
-
Wilson, D.A.1
Wilson, C.J.2
Rosen, B.M.3
Percec, V.4
-
49
-
-
84858627234
-
-
II-(σ-aryl) complexes as catalysts in the cyanation of bromothiophenes, see
-
II-(σ-aryl) complexes as catalysts in the cyanation of bromothiophenes, see:, J. V. Soolinger, H. D. Verkruijsse, M. A. Keegstra, L. Brandsma, Synth. Commun. 1990, 20, 3153-3156.
-
(1990)
Synth. Commun.
, vol.20
, pp. 3153-3156
-
-
Soolinger, J.V.1
Verkruijsse, H.D.2
Keegstra, M.A.3
Brandsma, L.4
-
50
-
-
79952132450
-
-
[3f,4d]
-
[3f,4d]
-
-
-
-
53
-
-
70349281534
-
-
C.-Y. Gao, X. Cao, L.-M. Yang, Org. Biomol. Chem. 2009, 7, 3922-3925.
-
(2009)
Org. Biomol. Chem.
, vol.7
, pp. 3922-3925
-
-
Gao, C.-Y.1
Cao, X.2
Yang, L.-M.3
-
54
-
-
79952129719
-
-
For the preparation of trans-haloarylbis(triphenylphosphane)nickel(II), see
-
For the preparation of trans-haloarylbis(triphenylphosphane)nickel(II), see
-
-
-
-
55
-
-
0016359350
-
-
in: (Eds.:, American Chemiscal Society, Washington, DC
-
L. Cassar, S. Ferrara, M. Foá, in: Advances in Chemistry (Eds.:, D. Forster, J. F. Roth), American Chemiscal Society, Washington, DC, 1974, vol. 132, p. 252.
-
(1974)
Advances in Chemistry
, vol.132
, pp. 252
-
-
Cassar, L.1
Ferrara, S.2
Foá, M.3
Forster, D.4
-
56
-
-
0003664601
-
-
Springer, New York
-
L. Brandsma, S. F. Vasilevsky, H. D. Verkruijsse, Application of Transition Metal Catalysts in Organic Synthesis, Springer, New York, 1998, pp. 3-4.
-
(1998)
Application of Transition Metal Catalysts in Organic Synthesis
, pp. 3-4
-
-
Brandsma, L.1
Vasilevsky, S.F.2
Verkruijsse, H.D.3
-
57
-
-
79952154528
-
-
2Cl] would be completely converted
-
2Cl] would be completely converted.
-
-
-
|