-
1
-
-
13444263825
-
-
For a recent review, see
-
For a recent review, see: Frisch, A. C; Beller, M. Angew. Chem., Int. Ed. 2005, 44, 674-688.
-
(2005)
Angew. Chem., Int. Ed
, vol.44
, pp. 674-688
-
-
Frisch, A.C.1
Beller, M.2
-
2
-
-
33751569703
-
-
Benzylic phosphonates/halides: (a) Molander, G. A.; Elia, M. D. J. Org. Chem. 2006, 71, 9198-9202.
-
Benzylic phosphonates/halides: (a) Molander, G. A.; Elia, M. D. J. Org. Chem. 2006, 71, 9198-9202.
-
-
-
-
3
-
-
0000985581
-
-
(b) Dohle, W.; Lindsay, D. M.; Knochel, P. Org. Lett. 2001, 3, 2871-2873.
-
(2001)
Org. Lett
, vol.3
, pp. 2871-2873
-
-
Dohle, W.1
Lindsay, D.M.2
Knochel, P.3
-
8
-
-
0028233573
-
-
Alkyl halides
-
(g) Yanagisawa, A.; Nomura, N.; Yamamoto, H. Tetrahedron 1994, 50, 6017-6028. Alkyl halides:
-
(1994)
Tetrahedron
, vol.50
, pp. 6017-6028
-
-
Yanagisawa, A.1
Nomura, N.2
Yamamoto, H.3
-
9
-
-
32444451793
-
-
(h) Ohmiya, H.; Wakabayashi, K.; Yorimitsu, H.; Oshima, K. Tetrahedron 2006, 62, 2207-2213.
-
(2006)
Tetrahedron
, vol.62
, pp. 2207-2213
-
-
Ohmiya, H.1
Wakabayashi, K.2
Yorimitsu, H.3
Oshima, K.4
-
10
-
-
0035904470
-
-
(i) Netherton, M. R.; Dai, C; Neuschutz, K.; Fu, G. C. J. Am. Chem. Soc. 2001, 123, 10099-10100.
-
(2001)
J. Am. Chem. Soc
, vol.123
, pp. 10099-10100
-
-
Netherton, M.R.1
Dai, C.2
Neuschutz, K.3
Fu, G.C.4
-
15
-
-
34250821753
-
-
(e) Strotman, N. A.; Sommer, S.; Fu, G. C. Angew. Chem., Int. Ed. 2007, 46, 3556-3558.
-
(2007)
Angew. Chem., Int. Ed
, vol.46
, pp. 3556-3558
-
-
Strotman, N.A.1
Sommer, S.2
Fu, G.C.3
-
16
-
-
0141940231
-
-
Alternative methods for accessing racemic tetraarylethanes: (a) Khurana, J. M.; Chauhan, S.; Maikap. G. C. Org. Bwmol. Chem. 2003, 1, 1737-1740.
-
Alternative methods for accessing racemic tetraarylethanes: (a) Khurana, J. M.; Chauhan, S.; Maikap. G. C. Org. Bwmol. Chem. 2003, 1, 1737-1740.
-
-
-
-
21
-
-
3242702956
-
-
(f) Wakui, H.; Kawasaki,.S.; Satoh. T.; Miura. M.; Nomura. M. J. Am. Chem. Soc. 2004, 126, 8658-8659.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 8658-8659
-
-
Wakui, H.1
Kawasaki, S.2
Satoh, T.3
Miura, M.4
Nomura, M.5
-
26
-
-
33846629495
-
-
Trappo, M. D.; Pollard, D.; Devine, P. Org. Lett. 2007, 9, 335-338.
-
(2007)
Org. Lett
, vol.9
, pp. 335-338
-
-
Trappo, M.D.1
Pollard, D.2
Devine, P.3
-
27
-
-
58149182091
-
-
The control reaction was run using these conditions on 31 in the presence of 1 equiv of pyridine to give 32 in 21% yield
-
The control reaction was run using these conditions on 31 in the presence of 1 equiv of pyridine to give 32 in 21% yield.
-
-
-
-
28
-
-
58149201686
-
-
It is well-established in the literature that Cu(I) combined with Grignard reagents forms organocuprates which can then undergo substitution reactions; for reviews, see:
-
It is well-established in the literature that Cu(I) combined with Grignard reagents forms organocuprates which can then undergo substitution reactions; for reviews, see:
-
-
-
-
30
-
-
0000936332
-
-
Erdik, E. Tetrahedron 1984, 40, 641-657. Therefore, it is possible that the observed dimerization occurs through a cuprate intermediate that goes on to form the observed product. Ullman biaryl coupling reactions are also wcll-documented as being catalyzed by Cu(I) via either a radical or a copper insertion pathway. For recent reviews, see:
-
(b) Erdik, E. Tetrahedron 1984, 40, 641-657. Therefore, it is possible that the observed dimerization occurs through a cuprate intermediate that goes on to form the observed product. Ullman biaryl coupling reactions are also wcll-documented as being catalyzed by Cu(I) via either a radical or a copper insertion pathway. For recent reviews, see:
-
-
-
-
31
-
-
0036589259
-
-
(c) Hassan, J.; Sevignon, M.; Gozzi, C; Lemaire. M. Chem. Rev. 2002, 102, 1359-1467.
-
(2002)
Chem. Rev
, vol.102
, pp. 1359-1467
-
-
Hassan, J.1
Sevignon, M.2
Gozzi, C.3
Lemaire, M.4
-
33
-
-
58149201685
-
-
2CuMgCl.MgCN (formed from 2i-PrMgCl + CuCN) produced none of the desired product 5.
-
2CuMgCl.MgCN" (formed from 2i-PrMgCl + CuCN) produced none of the desired product 5.
-
-
-
|