-
1
-
-
0001281066
-
-
(a) Doyle, M. P.; Loh, K.-L.; DeVries, K.; Chinn, M. S. Tetrahedron Lett. 1987, 28, 833.
-
(1987)
Tetrahedron Lett.
, vol.28
, pp. 833
-
-
Doyle, M.P.1
Loh, K.-L.2
DeVries, K.3
Chinn, M.S.4
-
2
-
-
84942708449
-
-
(b) Padwa, A.; Austin, D. J.; Hornbuckle, S. F.; Semones, M. A.; Doyle, M. P.; Protopova, M. N. J. Am. Chem. Soc. 1992, 114, 1874.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 1874
-
-
Padwa, A.1
Austin, D.J.2
Hornbuckle, S.F.3
Semones, M.A.4
Doyle, M.P.5
Protopova, M.N.6
-
3
-
-
0001183682
-
-
(c) Padwa, A.; Austin, D. J.; Price, A. T.; Semones, M. A.; Doyle, M. P.; Protopova, M. N.; Winchester, W. R.; Tran, A. J. Am. Chem. Soc. 1993, 115, 8669.
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 8669
-
-
Padwa, A.1
Austin, D.J.2
Price, A.T.3
Semones, M.A.4
Doyle, M.P.5
Protopova, M.N.6
Winchester, W.R.7
Tran, A.8
-
4
-
-
33748811198
-
-
For reviews see: (d) Padwa, A.; Austin, D. J. Angew. Chem., Int. Ed. Engl. 1994, 33, 1797.
-
(1994)
Angew. Chem., Int. Ed. Engl.
, vol.33
, pp. 1797
-
-
Padwa, A.1
Austin, D.J.2
-
5
-
-
52849093599
-
-
Karlin, K. D., Ed.; John Wiley & Sons: New York
-
(e) Doyle, M. P.; Ren, T. In Progress in Inorganic Chemistry; Karlin, K. D., Ed.; John Wiley & Sons: New York, 2001: Vol. 49, p 113.
-
(2001)
Progress in Inorganic Chemistry
, vol.49
, pp. 113
-
-
Doyle, M.P.1
Ren, T.2
-
7
-
-
37049094178
-
-
(a) Pellicciari, R.; Fringuelli, R.; Ceccherelli, R.; Sisani, E. J. Chem. Soc., Chem. Commun. 1979, 959.
-
(1979)
J. Chem. Soc., Chem. Commun.
, pp. 959
-
-
Pellicciari, R.1
Fringuelli, R.2
Ceccherelli, R.3
Sisani, E.4
-
8
-
-
0005748426
-
-
(b) Miyauchi, K.; Hori, K.; Hirai, T.; Takebayashi, M.; Ibata, T. Bull. Chem. Soc. Jpn. 1981, 54, 2142.
-
(1981)
Bull. Chem. Soc. Jpn.
, vol.54
, pp. 2142
-
-
Miyauchi, K.1
Hori, K.2
Hirai, T.3
Takebayashi, M.4
Ibata, T.5
-
9
-
-
0000181655
-
-
(c) Hudlicky, T.; Olivo, H. F.; Natchus, M. G.; Umpierrez, E. F.; Pandolfi, E.; Volonterio, C. J. Org. Chem. 1990, 55, 4767.
-
(1990)
J. Org. Chem.
, vol.55
, pp. 4767
-
-
Hudlicky, T.1
Olivo, H.F.2
Natchus, M.G.3
Umpierrez, E.F.4
Pandolfi, E.5
Volonterio, C.6
-
10
-
-
0001031980
-
-
(d) Taber, D. F.; Herr, R. J.; Pack, S. K.; Geremia, J. M. J. Org. Chem. 1996, 61, 2908.
-
(1996)
J. Org. Chem.
, vol.61
, pp. 2908
-
-
Taber, D.F.1
Herr, R.J.2
Pack, S.K.3
Geremia, J.M.4
-
11
-
-
0002282779
-
-
Small amounts of α-C-C migration (3-17%) have been reported with metal-free isopropylcarbene: (e) Mansoor, A. M.; Stevens, I. D. R. Tetrahedron Lett. 1966, 7, 1733.
-
(1966)
Tetrahedron Lett.
, vol.7
, pp. 1733
-
-
Mansoor, A.M.1
Stevens, I.D.R.2
-
12
-
-
0001469676
-
-
The 1,2-C-C migrations of metal carbenes have been observed when no other competing processes are possible: (a) Padwa, A.; Hornbuckle, S. F.; Zhang, Z.; Zhi, L. J. Org. Chem. 1990, 55, 5297.
-
(1990)
J. Org. Chem.
, vol.55
, pp. 5297
-
-
Padwa, A.1
Hornbuckle, S.F.2
Zhang, Z.3
Zhi, L.4
-
14
-
-
0037019671
-
-
(a) Aggarwal, V. K.; Sheldon, C. G.; Macdonald, G. J.; Martin, W. P. J. Am. Chem. Soc. 2002, 124, 10300.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 10300
-
-
Aggarwal, V.K.1
Sheldon, C.G.2
Macdonald, G.J.3
Martin, W.P.4
-
15
-
-
0002676988
-
-
(b) Reactions with commercial TMSD were very much lower yielding than TMSD made by us using the procedure described by Shioiri: Shioiri, T.; Aoyama, T.; Mori, S. Org. Synth. 1990, 68, 1.
-
(1990)
Org. Synth.
, vol.68
, pp. 1
-
-
Shioiri, T.1
Aoyama, T.2
Mori, S.3
-
16
-
-
0000038736
-
-
(a) Hosomi, A.; Hayashida, H.; Tominaga, Y. J. Org. Chem. 1989, 54, 3254.
-
(1989)
J. Org. Chem.
, vol.54
, pp. 3254
-
-
Hosomi, A.1
Hayashida, H.2
Tominaga, Y.3
-
17
-
-
0027445760
-
-
(b) Duhamel, L.; Gralak, J.; Bouyanzer, A. Tetrahedron Lett. 1993, 34, 7745.
-
(1993)
Tetrahedron Lett.
, vol.34
, pp. 7745
-
-
Duhamel, L.1
Gralak, J.2
Bouyanzer, A.3
-
20
-
-
33644641879
-
-
note
-
4-catalyzed decomposition of 4b at room temperature in either THF or toluene only gave recovery of starting material.
-
-
-
-
21
-
-
33644641746
-
-
note
-
Pivaldehyde was also examined, but the intermediate diazocompound related to 4 was too stable and did not decompose under either protocol A or B.
-
-
-
-
22
-
-
22244490671
-
-
The formation of cyclopropanes via 1,3-C-H insertion when competitive 1,2-C-H migration is also possible has recently been reported: Shi, W.; Zhang, B.; Zhang, J.; Liu, B.; Zhang, S.; Wang, J. Org. Lett. 2005, 7, 3103-3106.
-
(2005)
Org. Lett.
, vol.7
, pp. 3103-3106
-
-
Shi, W.1
Zhang, B.2
Zhang, J.3
Liu, B.4
Zhang, S.5
Wang, J.6
-
24
-
-
0000768901
-
-
For a discussion of early/late TS with different ligands on Rh, see: (a) Taber, D. F.; Hennessy, M. J.; Louey, J. P. J. Org. Chem. 1992, 57, 436-441.
-
(1992)
J. Org. Chem.
, vol.57
, pp. 436-441
-
-
Taber, D.F.1
Hennessy, M.J.2
Louey, J.P.3
-
26
-
-
84961985018
-
-
Nakamura, E.; Yoshikai, N.; Yamanaka, M. J. Am. Chem. Soc. 2002, 124, 7181-7192.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 7181-7192
-
-
Nakamura, E.1
Yoshikai, N.2
Yamanaka, M.3
-
27
-
-
0000234509
-
-
For an example of where substrate comformation dominates over electronic effects of ligands on Rh in primary/secondary C-H insertion, see: Doyle, M. P.; Westrum, L. J.; Wolthuis, W. N. E.; See, M. M.; Boone, W. P.; Bagheri, V.; Person, M. M. J. Am. Chem. Soc. 1993, 115, 958.
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 958
-
-
Doyle, M.P.1
Westrum, L.J.2
Wolthuis, W.N.E.3
See, M.M.4
Boone, W.P.5
Bagheri, V.6
Person, M.M.7
|