-
1
-
-
0000180645
-
-
(1) For representative examples of vinylcarbenoid transformations, see: (a) Davies, H. M. L. Aldrichimica Acta 1997, 30, 107.
-
(1997)
Aldrichimica Acta
, vol.30
, pp. 107
-
-
Davies, H.M.L.1
-
2
-
-
0029945485
-
-
(b) Davies, H. M. L.; Bruzinski, P. R.; Lake, D. H.; Kong, N.; Fall, M. J. J. Am. Chem. Soc. 1996, 118, 6897.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 6897
-
-
Davies, H.M.L.1
Bruzinski, P.R.2
Lake, D.H.3
Kong, N.4
Fall, M.J.5
-
3
-
-
0000558907
-
-
(c) Bulugahapitiya, P.; Landais, Y.; Parra-Rapado, L.; Planchenault, D.; Weber, V. J. Org. Chem. 1997, 62, 1630.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 1630
-
-
Bulugahapitiya, P.1
Landais, Y.2
Parra-Rapado, L.3
Planchenault, D.4
Weber, V.5
-
4
-
-
0031562398
-
-
(d) Davies, H. M. L.; Hansen, T.; Rutberg, J.; Bruzinski, P. R. Tetrahedon Lett. 1997, 38, 1741.
-
(1997)
Tetrahedon Lett.
, vol.38
, pp. 1741
-
-
Davies, H.M.L.1
Hansen, T.2
Rutberg, J.3
Bruzinski, P.R.4
-
5
-
-
0029950744
-
-
(2) For representative examples of phenylcarbenoid transformations, see: (a) Davies, H. M. L.; Bruzinski, P. R.; Fall, M. J. Tetrahedron Lett. 1996, 37, 4133.
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 4133
-
-
Davies, H.M.L.1
Bruzinski, P.R.2
Fall, M.J.3
-
6
-
-
0029941742
-
-
(b) Doyle, M. P.; Zhou, Q. -L.; Charnsangavej, C.; Longoria, M. A.; McKervey, M. A.; Garcia, C. F. Tetrahedron Lett. 1996, 37, 4129.
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 4129
-
-
Doyle, M.P.1
Zhou, Q.-L.2
Charnsangavej, C.3
Longoria, M.A.4
McKervey, M.A.5
Garcia, C.F.6
-
7
-
-
16044366523
-
-
(c) Buck, R. T.; Doyle, M. P.; Drysdale, M. J.; Ferris, L.; Forbes, D. C.; Haigh, D.; Moody, C. J.; Pearson, N. D.; Zhou, Q.-L. Tetrahedron Lett. 1996, 37, 7631.
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 7631
-
-
Buck, R.T.1
Doyle, M.P.2
Drysdale, M.J.3
Ferris, L.4
Forbes, D.C.5
Haigh, D.6
Moody, C.J.7
Pearson, N.D.8
Zhou, Q.-L.9
-
8
-
-
84987014061
-
-
(d) Paulini, K.; Reissig. H. -U. J. Prakt. Chem. 1995, 337, 55. Aller, E.; Cox, G. G.; Miller, D. J.; Moody, C. J. Tetrahedron Lett. 1994, 35, 5949.
-
(1995)
J. Prakt. Chem.
, vol.337
, pp. 55
-
-
Paulini, K.1
Reissig, H.-U.2
-
9
-
-
0027978020
-
-
(d) Paulini, K.; Reissig. H. -U. J. Prakt. Chem. 1995, 337, 55. Aller, E.; Cox, G. G.; Miller, D. J.; Moody, C. J. Tetrahedron Lett. 1994, 35, 5949.
-
(1994)
Tetrahedron Lett.
, vol.35
, pp. 5949
-
-
Aller, E.1
Cox, G.G.2
Miller, D.J.3
Moody, C.J.4
-
10
-
-
0000969629
-
-
(3) (a) Wulfman, D. S.; Pearce, B. W.; McDaniel Jr., R. S. Tetrahedron 1976, 32, 1251.
-
(1976)
Tetrahedron
, vol.32
, pp. 1251
-
-
Wulfman, D.S.1
Pearce, B.W.2
McDaniel R.S., Jr.3
-
14
-
-
1842640868
-
-
(6) For earlier examples of intermolecular C-H insertions, see: (a) Demonceau, A.; Noels, A. F.; Hubert, A. J.; Teyssie, P. J. Chem. Soc., Chem. Commun. 1981, 688.
-
(1981)
J. Chem. Soc., Chem. Commun.
, pp. 688
-
-
Demonceau, A.1
Noels, A.F.2
Hubert, A.J.3
Teyssie, P.4
-
15
-
-
84916142283
-
-
(b) Demonceau, A.; Noels, A. F.; Hubert, A. J.; Teyssie, P. J. Bull. Soc. Chim Belg. 1984, 93, 945.
-
(1984)
J. Bull. Soc. Chim Belg.
, vol.93
, pp. 945
-
-
Demonceau, A.1
Noels, A.F.2
Hubert, A.J.3
Teyssie, P.4
-
16
-
-
0024137280
-
-
(c) Demonceau, A.; Noels, A. F.; Hubert, A. J.; Teyssie, P. J. Mol. Catal. 1988, 49, L13.
-
(1988)
J. Mol. Catal.
, vol.49
-
-
Demonceau, A.1
Noels, A.F.2
Hubert, A.J.3
Teyssie, P.4
-
19
-
-
0001691695
-
-
(f) Adams, J. Poupart, M. A.; Greainer, L.; Schaller, C.; Quimet, N.; Frenette, R. Tetrahedron Lett. 1989, 30, 1749.
-
(1989)
Tetrahedron Lett.
, vol.30
, pp. 1749
-
-
Adams, J.1
Poupart, M.A.2
Greainer, L.3
Schaller, C.4
Quimet, N.5
Frenette, R.6
-
20
-
-
0000709206
-
-
(7) For recent reviews that discuss the status of intermolecular C-H insertions, see: (a) Ye, T.; McKervey, M. A. Chem. Rev. 1994, 94, 1091.
-
(1994)
Chem. Rev.
, vol.94
, pp. 1091
-
-
Ye, T.1
McKervey, M.A.2
-
21
-
-
0003394220
-
-
John Wiley & Sons, Inc.: New York
-
(b) Doyle, M. P.; McKervey, M. A.; Ye, T. Modern Catalytic Methods for Organic Synthesis with Diazo Compounds; John Wiley & Sons, Inc.: New York, 1997, pp 115.
-
(1997)
Modern Catalytic Methods for Organic Synthesis with Diazo Compounds
, pp. 115
-
-
Doyle, M.P.1
McKervey, M.A.2
Ye, T.3
-
22
-
-
84920311374
-
-
note
-
1H-decoupling experiments). Furthermore, irradiation of one of the C(4) protons (2.60 ppm) results in an nOe enhancement of the C(5) proton (5.81 ppm); irradiation of this C(5) proton results in enhancement of the same C(4) proton resonance. Additional nOe enhancements were observed between the C(3) and the C(4) protons, the C(5) and one of the C(6) protons, and the C(8) and one of the C(9) protons. (equation presented)
-
-
-
-
23
-
-
84987572853
-
-
(9) (a) Muller, P.; Pautex, N.; Doyle, M. P.; Bagheri, V. Helv. Chim. Acta 1990, 73, 1233.
-
(1990)
Helv. Chim. Acta
, vol.73
, pp. 1233
-
-
Muller, P.1
Pautex, N.2
Doyle, M.P.3
Bagheri, V.4
|