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Volumn 617-618, Issue , 2001, Pages 47-55

Recent progress in asymmetric intermolecular C-H activation by rhodium carbenoid intermediates

Author keywords

C H activation; Chiral catalysts; Rhodium carbenoid

Indexed keywords


EID: 0347716924     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-328X(00)00599-4     Document Type: Article
Times cited : (136)

References (62)
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    • For representative examples of intermolecular C-H insertions, see: (a) L.T. Scott, G.J. DeCicco, J. Am. Chem. Soc. 96 (1974) 322. (b) R.A. Ambramovitch, J. Roy, J. Chem. Soc. Chem. Commun. (1965) 542. (c) J. Adams, M.A. Poupart, L. Greainer, C. Schaller, N. Quimet, R. Frenette, Tetrahedron Lett. 30 (1989) 1749. (d) H.J. Callott, F. Metz, Tetrahedron Lett. 23 (1982) 4321. (e) H.J. Callott, F. Metz, Nouv. J. Chim. 9 (1985) 167. (f) A. Domenceau, A.F. Noels, J.L. Costa, A. Hubert, J. Mol. Catal. 58 (1990) 21.
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    • For representative examples of intermolecular C-H insertions, see: (a) L.T. Scott, G.J. DeCicco, J. Am. Chem. Soc. 96 (1974) 322. (b) R.A. Ambramovitch, J. Roy, J. Chem. Soc. Chem. Commun. (1965) 542. (c) J. Adams, M.A. Poupart, L. Greainer, C. Schaller, N. Quimet, R. Frenette, Tetrahedron Lett. 30 (1989) 1749. (d) H.J. Callott, F. Metz, Tetrahedron Lett. 23 (1982) 4321. (e) H.J. Callott, F. Metz, Nouv. J. Chim. 9 (1985) 167. (f) A. Domenceau, A.F. Noels, J.L. Costa, A. Hubert, J. Mol. Catal. 58 (1990) 21.
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    • For representative examples of intermolecular C-H insertions, see: (a) L.T. Scott, G.J. DeCicco, J. Am. Chem. Soc. 96 (1974) 322. (b) R.A. Ambramovitch, J. Roy, J. Chem. Soc. Chem. Commun. (1965) 542. (c) J. Adams, M.A. Poupart, L. Greainer, C. Schaller, N. Quimet, R. Frenette, Tetrahedron Lett. 30 (1989) 1749. (d) H.J. Callott, F. Metz, Tetrahedron Lett. 23 (1982) 4321. (e) H.J. Callott, F. Metz, Nouv. J. Chim. 9 (1985) 167. (f) A. Domenceau, A.F. Noels, J.L. Costa, A. Hubert, J. Mol. Catal. 58 (1990) 21.
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    • For representative examples of intermolecular C-H insertions, see: (a) L.T. Scott, G.J. DeCicco, J. Am. Chem. Soc. 96 (1974) 322. (b) R.A. Ambramovitch, J. Roy, J. Chem. Soc. Chem. Commun. (1965) 542. (c) J. Adams, M.A. Poupart, L. Greainer, C. Schaller, N. Quimet, R. Frenette, Tetrahedron Lett. 30 (1989) 1749. (d) H.J. Callott, F. Metz, Tetrahedron Lett. 23 (1982) 4321. (e) H.J. Callott, F. Metz, Nouv. J. Chim. 9 (1985) 167. (f) A. Domenceau, A.F. Noels, J.L. Costa, A. Hubert, J. Mol. Catal. 58 (1990) 21.
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    • For representative examples of intermolecular C-H insertions, see: (a) L.T. Scott, G.J. DeCicco, J. Am. Chem. Soc. 96 (1974) 322. (b) R.A. Ambramovitch, J. Roy, J. Chem. Soc. Chem. Commun. (1965) 542. (c) J. Adams, M.A. Poupart, L. Greainer, C. Schaller, N. Quimet, R. Frenette, Tetrahedron Lett. 30 (1989) 1749. (d) H.J. Callott, F. Metz, Tetrahedron Lett. 23 (1982) 4321. (e) H.J. Callott, F. Metz, Nouv. J. Chim. 9 (1985) 167. (f) A. Domenceau, A.F. Noels, J.L. Costa, A. Hubert, J. Mol. Catal. 58 (1990) 21.
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    • For representative examples of intermolecular C-H insertions, see: (a) L.T. Scott, G.J. DeCicco, J. Am. Chem. Soc. 96 (1974) 322. (b) R.A. Ambramovitch, J. Roy, J. Chem. Soc. Chem. Commun. (1965) 542. (c) J. Adams, M.A. Poupart, L. Greainer, C. Schaller, N. Quimet, R. Frenette, Tetrahedron Lett. 30 (1989) 1749. (d) H.J. Callott, F. Metz, Tetrahedron Lett. 23 (1982) 4321. (e) H.J. Callott, F. Metz, Nouv. J. Chim. 9 (1985) 167. (f) A. Domenceau, A.F. Noels, J.L. Costa, A. Hubert, J. Mol. Catal. 58 (1990) 21.
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    • For recent examples, see: (a)
    • For recent examples, see: (a) H.M.L. Davies, N. Kong, M.R. Churchill, J. Org. Chem. 63 (1998) 6586. (b) H.M.L. Davies, L. Rusiniak, Tetrahedron Lett. 39 (1998) 8811. (c) H.M.L. Davies, G. Ahmed, R.L. Calvo, M.R. Churchill, D.G. Churchill, J. Org. Chem. 63 (1998) 2641. (d) H.M.L. Davies, L.M. Hodges, C.T. Thornley, Tetrahedron Lett. 39 (1998) 2707. (e) H.M.L. Davies, B.D. Doan, J. Org. Chem. 63 (1998) 657. (f) H.M.L. Davies, D.G. Stafford, B.D. Doan, J.H. Houser, J. Am. Chem. Soc. 120 (1998) 3326.
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    • For recent examples, see: (a) H.M.L. Davies, N. Kong, M.R. Churchill, J. Org. Chem. 63 (1998) 6586. (b) H.M.L. Davies, L. Rusiniak, Tetrahedron Lett. 39 (1998) 8811. (c) H.M.L. Davies, G. Ahmed, R.L. Calvo, M.R. Churchill, D.G. Churchill, J. Org. Chem. 63 (1998) 2641. (d) H.M.L. Davies, L.M. Hodges, C.T. Thornley, Tetrahedron Lett. 39 (1998) 2707. (e) H.M.L. Davies, B.D. Doan, J. Org. Chem. 63 (1998) 657. (f) H.M.L. Davies, D.G. Stafford, B.D. Doan, J.H. Houser, J. Am. Chem. Soc. 120 (1998) 3326.
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    • For recent examples, see: (a) H.M.L. Davies, N. Kong, M.R. Churchill, J. Org. Chem. 63 (1998) 6586. (b) H.M.L. Davies, L. Rusiniak, Tetrahedron Lett. 39 (1998) 8811. (c) H.M.L. Davies, G. Ahmed, R.L. Calvo, M.R. Churchill, D.G. Churchill, J. Org. Chem. 63 (1998) 2641. (d) H.M.L. Davies, L.M. Hodges, C.T. Thornley, Tetrahedron Lett. 39 (1998) 2707. (e) H.M.L. Davies, B.D. Doan, J. Org. Chem. 63 (1998) 657. (f) H.M.L. Davies, D.G. Stafford, B.D. Doan, J.H. Houser, J. Am. Chem. Soc. 120 (1998) 3326.
    • (1998) J. Org. Chem. , vol.63 , pp. 2641
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    • (d)
    • For recent examples, see: (a) H.M.L. Davies, N. Kong, M.R. Churchill, J. Org. Chem. 63 (1998) 6586. (b) H.M.L. Davies, L. Rusiniak, Tetrahedron Lett. 39 (1998) 8811. (c) H.M.L. Davies, G. Ahmed, R.L. Calvo, M.R. Churchill, D.G. Churchill, J. Org. Chem. 63 (1998) 2641. (d) H.M.L. Davies, L.M. Hodges, C.T. Thornley, Tetrahedron Lett. 39 (1998) 2707. (e) H.M.L. Davies, B.D. Doan, J. Org. Chem. 63 (1998) 657. (f) H.M.L. Davies, D.G. Stafford, B.D. Doan, J.H. Houser, J. Am. Chem. Soc. 120 (1998) 3326.
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    • For recent examples, see: (a) H.M.L. Davies, N. Kong, M.R. Churchill, J. Org. Chem. 63 (1998) 6586. (b) H.M.L. Davies, L. Rusiniak, Tetrahedron Lett. 39 (1998) 8811. (c) H.M.L. Davies, G. Ahmed, R.L. Calvo, M.R. Churchill, D.G. Churchill, J. Org. Chem. 63 (1998) 2641. (d) H.M.L. Davies, L.M. Hodges, C.T. Thornley, Tetrahedron Lett. 39 (1998) 2707. (e) H.M.L. Davies, B.D. Doan, J. Org. Chem. 63 (1998) 657. (f) H.M.L. Davies, D.G. Stafford, B.D. Doan, J.H. Houser, J. Am. Chem. Soc. 120 (1998) 3326.
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    • For recent examples, see: (a) H.M.L. Davies, N. Kong, M.R. Churchill, J. Org. Chem. 63 (1998) 6586. (b) H.M.L. Davies, L. Rusiniak, Tetrahedron Lett. 39 (1998) 8811. (c) H.M.L. Davies, G. Ahmed, R.L. Calvo, M.R. Churchill, D.G. Churchill, J. Org. Chem. 63 (1998) 2641. (d) H.M.L. Davies, L.M. Hodges, C.T. Thornley, Tetrahedron Lett. 39 (1998) 2707. (e) H.M.L. Davies, B.D. Doan, J. Org. Chem. 63 (1998) 657. (f) H.M.L. Davies, D.G. Stafford, B.D. Doan, J.H. Houser, J. Am. Chem. Soc. 120 (1998) 3326.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 3326
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    • (b) in: M.E. Haramata (Ed.) JAI Press
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