-
1
-
-
27644465867
-
-
For recent progress, see: a
-
For recent progress, see: (a) Maki, T.; Ishihara, K.; Yamamoto, H. Org. Lett. 2005, 7, 5043-5046.
-
(2005)
Org. Lett
, vol.7
, pp. 5043-5046
-
-
Maki, T.1
Ishihara, K.2
Yamamoto, H.3
-
2
-
-
34547896611
-
-
(b) Gunanathan, C.; Ben-David, Y.; Milstein, D. Science 2007, 317, 790-792.
-
(2007)
Science
, vol.317
, pp. 790-792
-
-
Gunanathan, C.1
Ben-David, Y.2
Milstein, D.3
-
5
-
-
33746190644
-
-
(a) Bode, J. W.; Fox, R. M.; Baucom, K. D. Angew. Chem., Int. Ed. 2006, 45, 1248-1252.
-
(2006)
Angew. Chem., Int. Ed
, vol.45
, pp. 1248-1252
-
-
Bode, J.W.1
Fox, R.M.2
Baucom, K.D.3
-
6
-
-
32244438956
-
-
(b) Carrillo, N.; Davalos, E. A.; Russak, J. A. J. Am. Chem. Soc. 2006, 128, 1452-1453.
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 1452-1453
-
-
Carrillo, N.1
Davalos, E.A.2
Russak, J.A.3
-
9
-
-
3543074145
-
-
(a) Reynolds, N. T.; Read de Alaniz, J.; Rovis, T. J. Am. Chem. Soc. 2004, 126, 9518-9519.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 9518-9519
-
-
Reynolds, N.T.1
Read de Alaniz, J.2
Rovis, T.3
-
14
-
-
33748807069
-
-
Sohn, S. S.; Bode, J. W. Angew. Chem., Int. Ed. 2006, 45, 6021-6024.
-
(2006)
Angew. Chem., Int. Ed
, vol.45
, pp. 6021-6024
-
-
Sohn, S.S.1
Bode, J.W.2
-
15
-
-
34548522013
-
-
(a) Li, G.-Q.; Li, Y.; Dai, L.-X.; You, S.-L. Org. Lett. 2007, 9, 3519-3521.
-
(2007)
Org. Lett
, vol.9
, pp. 3519-3521
-
-
Li, G.-Q.1
Li, Y.2
Dai, L.-X.3
You, S.-L.4
-
16
-
-
2942629617
-
-
(b) Alcaide, B.; Almendros, P.; Redondo, M. C. Org. Lett. 2004, 6, 1765-1767.
-
(2004)
Org. Lett
, vol.6
, pp. 1765-1767
-
-
Alcaide, B.1
Almendros, P.2
Redondo, M.C.3
-
17
-
-
20544443754
-
-
Acyl azolium salts appear to exhibit an inherent preference to nucleophilic substitution reactions with oxygen and sulfur nucleophiles; see: Movassaghi, M, Schmidt, M. A. Org. Lett. 2005, 7, 2453-2456
-
Acyl azolium salts appear to exhibit an inherent preference to nucleophilic substitution reactions with oxygen and sulfur nucleophiles; see: Movassaghi, M.; Schmidt, M. A. Org. Lett. 2005, 7, 2453-2456.
-
-
-
-
18
-
-
36148942303
-
-
Contemporaneously, Rovis has reported a similar redox amidation utilizing HOAt as a promoter: Vora, H. U.; Rovis, T. J. Am. Chem. Soc. 2007, 129, in press.
-
Contemporaneously, Rovis has reported a similar redox amidation utilizing HOAt as a promoter: Vora, H. U.; Rovis, T. J. Am. Chem. Soc. 2007, 129, in press.
-
-
-
-
19
-
-
33845202285
-
-
He, M.; Uc, G. J.; Bode, J. W. J. Am. Chem. Soc. 2006, 128, 15088-15089.
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 15088-15089
-
-
He, M.1
Uc, G.J.2
Bode, J.W.3
-
20
-
-
7744232978
-
-
(a) Sohn, S. S.; Rosen, E. L.; Bode, J. W. J. Am. Chem. Soc. 2004, 126, 14370-14371.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 14370-14371
-
-
Sohn, S.S.1
Rosen, E.L.2
Bode, J.W.3
-
21
-
-
10044249952
-
-
(b) Burstein, C.; Glorius, F. Angew. Chem., Int. Ed. 2004, 43, 6205-6208.
-
(2004)
Angew. Chem., Int. Ed
, vol.43
, pp. 6205-6208
-
-
Burstein, C.1
Glorius, F.2
-
22
-
-
33746584001
-
-
(c) Burstein, C.; Tschan, S.; Xie, X.; Glorius, F. Synthesis 2006, 2418-2439.
-
(2006)
Synthesis
, pp. 2418-2439
-
-
Burstein, C.1
Tschan, S.2
Xie, X.3
Glorius, F.4
-
24
-
-
33845191735
-
-
Dirksen, A.; Hackeng, T. M.; Dawson, P. E. Angew. Chem., Int. Ed. 2006, 45, 7581-7584.
-
(2006)
Angew. Chem., Int. Ed
, vol.45
, pp. 7581-7584
-
-
Dirksen, A.1
Hackeng, T.M.2
Dawson, P.E.3
-
25
-
-
36148931213
-
-
For the only two exceptions, see examples cited in refs 6a and 7b
-
For the only two exceptions, see examples cited in refs 6a and 7b.
-
-
-
|