Enantioselective [2,3] sigmatropic rearrangement mediated by a butyllithium-chiral ligand complex

Chemical Communications

Volumn , Issue 8, 1997, Pages 737-738

  Manabe, Shino ^a,b  

^a UNIVERSITY OF TOKYO   (Japan)

^b INST OF PHYS AND CHEMICAL RESEARCH   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0001661548     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/a700906b     Document Type: Article

References (25)

1. For recent reviews see: T. Nakai and K. Mikami, Org. React., 1994, 46, 105; J. A. Marshall, in Comprehensive Organic Synthesis, ed. B. M. Trost and I. Fleming, Pergamon, London, 1991, vol. 3, pp. 975-1014; R. Brückner, in Comprehensive Organic Synthesis, ed. B. M. Trost and I. Fleming, Pergamon, London, 1991, vol. 6, pp. 873-908.
2. For recent reviews see: T. Nakai and K. Mikami, Org. React., 1994, 46, 105; J. A. Marshall, in Comprehensive Organic Synthesis, ed. B. M. Trost and I. Fleming, Pergamon, London, 1991, vol. 3, pp. 975-1014; R. Brückner, in Comprehensive Organic Synthesis, ed. B. M. Trost and I. Fleming, Pergamon, London, 1991, vol. 6, pp. 873-908.
3. For recent reviews see: T. Nakai and K. Mikami, Org. React., 1994, 46, 105; J. A. Marshall, in Comprehensive Organic Synthesis, ed. B. M. Trost and I. Fleming, Pergamon, London, 1991, vol. 3, pp. 975-1014; R. Brückner, in Comprehensive Organic Synthesis, ed. B. M. Trost and I. Fleming, Pergamon, London, 1991, vol. 6, pp. 873-908.
4. K. Mikami, O. Takahashi, T. Kasuga and T. Nakai, Chem. Lett., 1985, 1729; K. Mikami, K. Fujimoto, T. Kasuga and T. Nakai, Tetrahedron Lett., 1984, 25, 6011; O. Takahashi, K. Mikami and T. Nakai, Chem. Lett., 1987, 69; D. Enders, D. Backhaus and J. Runsink, Angew. Chem., Int. Ed. Engl., 1994, 33, 2098; D. Enders and D. Backhaus, Synlett, 1995, 631.
5. K. Mikami, O. Takahashi, T. Kasuga and T. Nakai, Chem. Lett., 1985, 1729; K. Mikami, K. Fujimoto, T. Kasuga and T. Nakai, Tetrahedron Lett., 1984, 25, 6011; O. Takahashi, K. Mikami and T. Nakai, Chem. Lett., 1987, 69; D. Enders, D. Backhaus and J. Runsink, Angew. Chem., Int. Ed. Engl., 1994, 33, 2098; D. Enders and D. Backhaus, Synlett, 1995, 631.
6. K. Mikami, O. Takahashi, T. Kasuga and T. Nakai, Chem. Lett., 1985, 1729; K. Mikami, K. Fujimoto, T. Kasuga and T. Nakai, Tetrahedron Lett., 1984, 25, 6011; O. Takahashi, K. Mikami and T. Nakai, Chem. Lett., 1987, 69; D. Enders, D. Backhaus and J. Runsink, Angew. Chem., Int. Ed. Engl., 1994, 33, 2098; D. Enders and D. Backhaus, Synlett, 1995, 631.
7. K. Mikami, O. Takahashi, T. Kasuga and T. Nakai, Chem. Lett., 1985, 1729; K. Mikami, K. Fujimoto, T. Kasuga and T. Nakai, Tetrahedron Lett., 1984, 25, 6011; O. Takahashi, K. Mikami and T. Nakai, Chem. Lett., 1987, 69; D. Enders, D. Backhaus and J. Runsink, Angew. Chem., Int. Ed. Engl., 1994, 33, 2098; D. Enders and D. Backhaus, Synlett, 1995, 631.
8. K. Mikami, O. Takahashi, T. Kasuga and T. Nakai, Chem. Lett., 1985, 1729; K. Mikami, K. Fujimoto, T. Kasuga and T. Nakai, Tetrahedron Lett., 1984, 25, 6011; O. Takahashi, K. Mikami and T. Nakai, Chem. Lett., 1987, 69; D. Enders, D. Backhaus and J. Runsink, Angew. Chem., Int. Ed. Engl., 1994, 33, 2098; D. Enders and D. Backhaus, Synlett, 1995, 631.
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14. S. Matsui (Manabe), M. Nakajima and K. Koga, 7th IUPAC Symposium on Organometallic Chemistry directed towards Organic Synthesis (OMCOS 7), abstract 2B, Kobe, September, 1993; Nakai's group has also shown that this type of reaction proceeds in 70% ee: K. Tomooka, N. Komine and T. Nakai, The Japan Chemical Society annual meeting, abstract II 1208, Tokyo, March, 1996.
15. S. Matsui (Manabe), M. Nakajima and K. Koga, 7th IUPAC Symposium on Organometallic Chemistry directed towards Organic Synthesis (OMCOS 7), abstract 2B, Kobe, September, 1993; Nakai's group has also shown that this type of reaction proceeds in 70% ee: K. Tomooka, N. Komine and T. Nakai, The Japan Chemical Society annual meeting, abstract II 1208, Tokyo, March, 1996.
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