-
1
-
-
20544450502
-
-
2 nd ed. (Eds.: A. de Meijere, F. Diederich), Wiley-VCH, Weinheim.
-
See the Supporting Information for details.: Metal-Catalyzed Cross-Coupling Reactions, 2 nd ed., (Eds.: A. de Meijere, F. Diederich,), Wiley-VCH, Weinheim, 2004.
-
(2004)
Metal-Catalyzed Cross-Coupling Reactions
-
-
-
7
-
-
0036589259
-
-
J. Hassan, M. Sevignon, C. Gozzi, E. Schulz, M. Lemaire, Chem. Rev. 2002, 102, 1359
-
(2002)
Chem. Rev.
, vol.102
, pp. 1359
-
-
Hassan, J.1
Sevignon, M.2
Gozzi, C.3
Schulz, E.4
Lemaire, M.5
-
8
-
-
0037175592
-
-
S. Kotha, K. Lahiri, D. Kashinath, Tetrahedron 2002, 58, 9633
-
(2002)
Tetrahedron
, vol.58
, pp. 9633
-
-
Kotha, S.1
Lahiri, K.2
Kashinath, D.3
-
14
-
-
39749179066
-
-
F. Alonso, I. P. Beletskaya, M. Yus, Tetrahedron 2008, 64, 3047
-
(2008)
Tetrahedron
, vol.64
, pp. 3047
-
-
Alonso, F.1
Beletskaya, I.P.2
Yus, M.3
-
15
-
-
84890973385
-
-
(Ed.: L. Ackermann), Wiley-VCH, Weinheim.
-
Modern Arylation Methods (Ed.:, L. Ackermann,), Wiley-VCH, Weinheim, 2009.
-
(2009)
Modern Arylation Methods
-
-
-
16
-
-
0037138687
-
-
For selected examples, see: J. Yin, M. P. Rainka, X. X. Zhang, S. L. Buchwald, J. Am. Chem. Soc. 2002, 124, 1162
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 1162
-
-
Yin, J.1
Rainka, M.P.2
Zhang, X.X.3
Buchwald, S.L.4
-
17
-
-
1842717280
-
-
G. Altenhoff, R. Goddard, C. W. Lehmann, F. Glorius, Angew. Chem. 2003, 115, 3818
-
(2003)
Angew. Chem.
, vol.115
, pp. 3818
-
-
Altenhoff, G.1
Goddard, R.2
Lehmann, C.W.3
Glorius, F.4
-
19
-
-
0345802559
-
-
O. Navarro, R. A. Kelly, S. P. Nolan, J. Am. Chem. Soc. 2003, 125, 16194
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 16194
-
-
Navarro, O.1
Kelly, R.A.2
Nolan, S.P.3
-
20
-
-
4544372693
-
-
S. D. Walker, T. E. Barder, J. R. Martinelli, S. L. Buchwald, Angew. Chem. 2004, 116, 1907
-
(2004)
Angew. Chem.
, vol.116
, pp. 1907
-
-
Walker, S.D.1
Barder, T.E.2
Martinelli, J.R.3
Buchwald, S.L.4
-
22
-
-
16844367937
-
-
T. E. Barder, S. D. Walker, J. R. Martinelli, S. L. Buchwald, J. Am. Chem. Soc. 2005, 127, 4685
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 4685
-
-
Barder, T.E.1
Walker, S.D.2
Martinelli, J.R.3
Buchwald, S.L.4
-
23
-
-
33645451955
-
-
N. Marion, O. Navarro, J. Mei, E. D. Stevens, N. M. Scott, S. P. Nolan, J. Am. Chem. Soc. 2006, 128, 4101
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 4101
-
-
Marion, N.1
Navarro, O.2
Mei, J.3
Stevens, E.D.4
Scott, N.M.5
Nolan, S.P.6
-
24
-
-
46249120102
-
-
O. Diebolt, P. Braunstein, S. P. Nolan, C. S. J. Cazin, Chem. Commun. 2008, 3190
-
(2008)
Chem. Commun.
, pp. 3190
-
-
Diebolt, O.1
Braunstein, P.2
Nolan, S.P.3
Cazin, C.S.J.4
-
25
-
-
79953045638
-
-
W. Tang, A. G. Capacci, X. Wei, W. Li, A. White, N. D. Patel, J. Savoie, J. J. Gao, S. Rodriguez, B. Qu, N. Haddad, B. Z. Lu, D. Krishnamurthy, N. K. Yee, C. H. Senanayake, Angew. Chem. 2010, 122, 6015
-
(2010)
Angew. Chem.
, vol.122
, pp. 6015
-
-
Tang, W.1
Capacci, A.G.2
Wei, X.3
Li, W.4
White, A.5
Patel, N.D.6
Savoie, J.7
Gao, J.J.8
Rodriguez, S.9
Qu, B.10
Haddad, N.11
Lu, B.Z.12
Krishnamurthy, D.13
Yee, N.K.14
Senanayake, C.H.15
-
27
-
-
11444254369
-
-
For two examples of Kumada couplings at elevated temperatures, see
-
For efficient tetra-ortho-substituted biaryl formation starting from aryl bromides with appropriate heating, see references [4a, d, e, h]. For two examples of Stille couplings at elevated temperatures, see: W. Su, S. Urgaonkar, P. A. McLaughlin, J. G. Verkade, J. Am. Chem. Soc. 2004, 126, 16433. For two examples of Kumada couplings at elevated temperatures, see
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 16433
-
-
Su, W.1
Urgaonkar, S.2
McLaughlin, P.A.3
Verkade, J.G.4
-
28
-
-
66149142155
-
-
For two examples of Negishi couplings at elevated temperature, see
-
C. E. Hartmann, S. P. Nolan, C. S. J. Cazin, Organometallics 2009, 28, 2915. For two examples of Negishi couplings at elevated temperature, see
-
(2009)
Organometallics
, vol.28
, pp. 2915
-
-
Hartmann, C.E.1
Nolan, S.P.2
Cazin, C.S.J.3
-
29
-
-
5644254180
-
-
For a series of examples of Negishi couplings that proceed at room temperature or slightly above, underlining the higher reactivity compared to Suzuki-Miyaura couplings, see
-
J. E. Milne, S. L. Buchwald, J. Am. Chem. Soc. 2004, 126, 13028. For a series of examples of Negishi couplings that proceed at room temperature or slightly above, underlining the higher reactivity compared to Suzuki-Miyaura couplings, see
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 13028
-
-
Milne, J.E.1
Buchwald, S.L.2
-
30
-
-
77956893606
-
-
S. Çalimsiz, M. Sayah, D. Mallik, M. G. Organ, Angew. Chem. 2010, 122, 2058
-
(2010)
Angew. Chem.
, vol.122
, pp. 2058
-
-
Çalimsiz, S.1
Sayah, M.2
Mallik, D.3
Organ, M.G.4
-
32
-
-
9344240844
-
-
for a review on the use of NHC ligands in LTM catalysis, see
-
G. Altenhoff, R. Goddard, C. W. Lehmann, F. Glorius, J. Am. Chem. Soc. 2004, 126, 15195; for a review on the use of NHC ligands in LTM catalysis, see
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 15195
-
-
Altenhoff, G.1
Goddard, R.2
Lehmann, C.W.3
Glorius, F.4
-
33
-
-
84908659806
-
-
S. Díez-González, N. Marion, S. P. Nolan, Chem. Rev. 2009, 109, 3612.
-
(2009)
Chem. Rev.
, vol.109
, pp. 3612
-
-
Díez-González, S.1
Marion, N.2
Nolan, S.P.3
-
34
-
-
76149119399
-
-
M. G. Organ, S. Çalimsiz, M. Sayah, K. H. Hoi, A. J. Lough, Angew. Chem. 2009, 121, 2419
-
(2009)
Angew. Chem.
, vol.121
, pp. 2419
-
-
Organ, M.G.1
Çalimsiz, S.2
Sayah, M.3
Hoi, K.H.4
Lough, A.J.5
-
36
-
-
47049100485
-
-
T. Hoshi, T. Nakazawa, I. Saitoh, A. Mori, T. Suzuki, J. Sakai, H. Hagiwara, Org. Lett. 2008, 10, 2063
-
(2008)
Org. Lett.
, vol.10
, pp. 2063
-
-
Hoshi, T.1
Nakazawa, T.2
Saitoh, I.3
Mori, A.4
Suzuki, T.5
Sakai, J.6
Hagiwara, H.7
-
37
-
-
77749298298
-
-
L. Ackermann, H. K. Potukuchi, A. Althammer, R. Born, P. Meyer, Org. Lett. 2010, 12, 1004
-
(2010)
Org. Lett.
, vol.12
, pp. 1004
-
-
Ackermann, L.1
Potukuchi, H.K.2
Althammer, A.3
Born, R.4
Meyer, P.5
-
39
-
-
77954790864
-
-
C. M. So, W. K. Chow, P. Y. Choy, C. P. Lau, F. Y. Kwong, Chem. Eur. J. 2010, 16, 7996
-
(2010)
Chem. Eur. J.
, vol.16
, pp. 7996
-
-
So, C.M.1
Chow, W.K.2
Choy, P.Y.3
Lau, C.P.4
Kwong, F.Y.5
-
42
-
-
44349094826
-
-
X. Luan, R. Mariz, M. Gatti, C. Costabile, A. Poater, L. Cavallo, A. Linden, R. Dorta, J. Am. Chem. Soc. 2008, 130, 6848
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 6848
-
-
Luan, X.1
Mariz, R.2
Gatti, M.3
Costabile, C.4
Poater, A.5
Cavallo, L.6
Linden, A.7
Dorta, R.8
-
43
-
-
66149172263
-
-
For the synthesis of more members of the same ligand family, see
-
L. Vieille-Petit, X. Luan, R. Mariz, S. Blumentritt, A. Linden, R. Dorta, Eur. J. Inorg. Chem. 2009, 1861. For the synthesis of more members of the same ligand family, see
-
(2009)
Eur. J. Inorg. Chem.
, pp. 1861
-
-
Vieille-Petit, L.1
Luan, X.2
Mariz, R.3
Blumentritt, S.4
Linden, A.5
Dorta, R.6
-
44
-
-
79955368585
-
-
M. Gatti, L. Wu, E. Drinkel, F. Gaggia, S. Blumentritt, A. Linden, R. Dorta, ARKIVOC 2011, 6, 176.
-
(2011)
ARKIVOC
, vol.6
, pp. 176
-
-
Gatti, M.1
Wu, L.2
Drinkel, E.3
Gaggia, F.4
Blumentritt, S.5
Linden, A.6
Dorta, R.7
-
45
-
-
60949084790
-
-
X. Luan, R. Mariz, C. Robert, M. Gatti, S. Blumentritt, A. Linden, R. Dorta, Org. Lett. 2008, 10, 5569
-
(2008)
Org. Lett.
, vol.10
, pp. 5569
-
-
Luan, X.1
Mariz, R.2
Robert, C.3
Gatti, M.4
Blumentritt, S.5
Linden, A.6
Dorta, R.7
-
46
-
-
77951838398
-
-
X. Luan, L. Wu, E. Drinkel, R. Mariz, M. Gatti, R. Dorta, Org. Lett. 2010, 12, 1912.
-
(2010)
Org. Lett.
, vol.12
, pp. 1912
-
-
Luan, X.1
Wu, L.2
Drinkel, E.3
Mariz, R.4
Gatti, M.5
Dorta, R.6
-
47
-
-
78651237614
-
-
A. Poater, F. Ragone, R. Mariz, R. Dorta, L. Cavallo, Chem. Eur. J. 2010, 16, 14348
-
(2010)
Chem. Eur. J.
, vol.16
, pp. 14348
-
-
Poater, A.1
Ragone, F.2
Mariz, R.3
Dorta, R.4
Cavallo, L.5
-
48
-
-
66149192545
-
-
A. Poater, B. Cosenza, A. Correa, S. Giudice, F. Ragone, V. Scarano, L. Cavallo, Eur. J. Inorg. Chem. 2009, 1759
-
(2009)
Eur. J. Inorg. Chem.
, pp. 1759
-
-
Poater, A.1
Cosenza, B.2
Correa, A.3
Giudice, S.4
Ragone, F.5
Scarano, V.6
Cavallo, L.7
-
49
-
-
0142227781
-
-
A. C. Hillier, W. J. Sommer, B. S. Yong, J. L. Petersen, L. Cavallo, S. P. Nolan, Organometallics 2003, 22, 4322
-
(2003)
Organometallics
, vol.22
, pp. 4322
-
-
Hillier, A.C.1
Sommer, W.J.2
Yong, B.S.3
Petersen, J.L.4
Cavallo, L.5
Nolan, S.P.6
-
51
-
-
79955678637
-
-
P. Liu, J. Montgomery, K. N. Houk, J. Am. Chem. Soc. 2011, 133, 6956.
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 6956
-
-
Liu, P.1
Montgomery, J.2
Houk, K.N.3
-
52
-
-
38949179137
-
-
R. A. Kelly III, H. Clavier, S. Giudice, N. M. Scott, E. D. Stevens, J. Bordner, I. Samardjiev, C. D. Hoff, L. Cavallo, S. P. Nolan, Organometallics 2008, 27, 202.
-
(2008)
Organometallics
, vol.27
, pp. 202
-
-
Clavier, H.1
Giudice, S.2
Scott, N.M.3
Stevens, E.D.4
Bordner, J.5
Samardjiev, I.6
Hoff, C.D.7
Cavallo, L.8
Nolan, S.P.9
-
53
-
-
67749093251
-
-
I. C. Stewart, D. Benitez, D. J. O'Leary, E. Tkatchouk, M. W. Day, W. A. Goddard, R. H. Grubbs, J. Am. Chem. Soc. 2009, 131, 1931
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 1931
-
-
Stewart, I.C.1
Benitez, D.2
O'Leary, D.J.3
Tkatchouk, E.4
Day, M.W.5
Goddard, W.A.6
Grubbs, R.H.7
-
54
-
-
77950202768
-
-
F. Ragone, A. Poater, L. Cavallo, J. Am. Chem. Soc. 2010, 132, 4249.
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 4249
-
-
Ragone, F.1
Poater, A.2
Cavallo, L.3
|