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Recent review articles: a) B. Giese, Radicals in Organic Synthesis: Formation of Carbon - Carbon Bonds, Pergamon, Oxford, 1986; b) G. Pattenden, Chem. Soc. Rev. 1988, 17, 361-382; c) D.P. Curran in Comprehensive Organic Synthesis, Vol. 4 (Eds.: B. M. Trost, I. Fleming, M. F. Semmelhock), Pergamon, Oxford, 1991, p. 715; d) C. P. Jasperse, D. P. Curran, T. L. Fevig, Chem. Rev. 1991, 91, 1237-1286; e) W. B. Motherwell, D. Crich, Free-Radical Reactions in Organic Synthesis, Academic Press, London, 1992; f) A. L. J. Beckwith, Chem. Soc. Rev. 1993, 143-151; g) G. G. Melikyan, Synthesis 1993, 833-850; h) G. A. Molander, C. R. Harris, Chem. Rev. 1996, 96, 307-338; i) B. B. Snider, Chem. Rev. 1996, 96, 339-363; j) S. Z. Zard, Angew. Chem. 1997, 109, 723-737; Angew. Chem. Int. Ed. Engl. 1997, 36, 673-685.
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Recent review articles: a) B. Giese, Radicals in Organic Synthesis: Formation of Carbon - Carbon Bonds, Pergamon, Oxford, 1986; b) G. Pattenden, Chem. Soc. Rev. 1988, 17, 361-382; c) D.P. Curran in Comprehensive Organic Synthesis, Vol. 4 (Eds.: B. M. Trost, I. Fleming, M. F. Semmelhock), Pergamon, Oxford, 1991, p. 715; d) C. P. Jasperse, D. P. Curran, T. L. Fevig, Chem. Rev. 1991, 91, 1237-1286; e) W. B. Motherwell, D. Crich, Free-Radical Reactions in Organic Synthesis, Academic Press, London, 1992; f) A. L. J. Beckwith, Chem. Soc. Rev. 1993, 143-151; g) G. G. Melikyan, Synthesis 1993, 833-850; h) G. A. Molander, C. R. Harris, Chem. Rev. 1996, 96, 307-338; i) B. B. Snider, Chem. Rev. 1996, 96, 339-363; j) S. Z. Zard, Angew. Chem. 1997, 109, 723-737; Angew. Chem. Int. Ed. Engl. 1997, 36, 673-685.
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B. J. Maxwell, J. Tsanaktsidis, J. Chem. Soc. Chem. Commun. 1994, 533-534; W. R. Bowman, P. T. Stephenson, A. R. Young, Tetrahedron 1996, 52, 11445-11462. See also the reaction in the presence of redox systems: F. Minisci, Acc. Chem. Res. 1975, 8, 165-171; J.-L. Bourgeois, L. Stella, J.-M. Surzur, Tetrahedron Lett. 1981, 22, 61-64; L. Stella, Angew. Chem. 1983, 95, 368-80; Angew. Chem. Int. Ed. Engl. 1983, 22, 337-349.
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B. J. Maxwell, J. Tsanaktsidis, J. Chem. Soc. Chem. Commun. 1994, 533-534; W. R. Bowman, P. T. Stephenson, A. R. Young, Tetrahedron 1996, 52, 11445-11462. See also the reaction in the presence of redox systems: F. Minisci, Acc. Chem. Res. 1975, 8, 165-171; J.-L. Bourgeois, L. Stella, J.-M. Surzur, Tetrahedron Lett. 1981, 22, 61-64; L. Stella, Angew. Chem. 1983, 95, 368-80; Angew. Chem. Int. Ed. Engl. 1983, 22, 337-349.
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B. J. Maxwell, J. Tsanaktsidis, J. Chem. Soc. Chem. Commun. 1994, 533-534; W. R. Bowman, P. T. Stephenson, A. R. Young, Tetrahedron 1996, 52, 11445-11462. See also the reaction in the presence of redox systems: F. Minisci, Acc. Chem. Res. 1975, 8, 165-171; J.-L. Bourgeois, L. Stella, J.-M. Surzur, Tetrahedron Lett. 1981, 22, 61-64; L. Stella, Angew. Chem. 1983, 95, 368-80; Angew. Chem. Int. Ed. Engl. 1983, 22, 337-349.
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B. J. Maxwell, J. Tsanaktsidis, J. Chem. Soc. Chem. Commun. 1994, 533-534; W. R. Bowman, P. T. Stephenson, A. R. Young, Tetrahedron 1996, 52, 11445-11462. See also the reaction in the presence of redox systems: F. Minisci, Acc. Chem. Res. 1975, 8, 165-171; J.-L. Bourgeois, L. Stella, J.-M. Surzur, Tetrahedron Lett. 1981, 22, 61-64; L. Stella, Angew. Chem. 1983, 95, 368-80; Angew. Chem. Int. Ed. Engl. 1983, 22, 337-349.
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note
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[2a]
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53
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0345139438
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For a related early example involving lithium alcoholate see ref. [1a]
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For a related early example involving lithium alcoholate see ref. [1a], p. 63.
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Shay, J.J.2
Ji, J.3
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