The photochemistry of 3-heteroatom substituted 1,4-dienes

Author:

Leone Andrea A.,Mariano Patrick S.

Publisher

Springer Science and Business Media LLC

Subject

General Engineering,General Chemistry

Reference89 articles.

1. Current address: Department of Chemistry, The University of Maryland, College Park, Maryland 20742.

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3. (a) R. Huisgen, E. Funke, H. Gotthardt, and H. Panke,Chem. Ber.,104, 1532 (1971); (b) E. Braun, E. Funke, H. Gotthardt, and R. Huisgen,Chem. Ber.,104, 1562 (1971); (c) E. Funke, R. Huisgen, and F. C. Schaefer,Chem. Ber.,104 1550 (1971).

4. (a) J. W. Lown,Rec. Chem. Account Prog.,32, 51 (1971); (b) M. P. Cava and M. V. Lakshmikanthan,Account Chem. Res.,8, 139 (1975); (c). C. G. Stuckwish,Synthesis, 469 (1973); (d) W. Baker and D. Ollis,Quart. Rev.,11, 15 (1957); (e) R. M. Kellogg,Tetrahedron,32, 2165 (1976); (f) E. F. Ullman,Account Chem. Res.,1, 353 (1968); (g) D. R. Arnold, A. B. Evnin, and L. A. Karnischky,Pure Appl. Chem.,24, 523 (1970); (h) J. C. Earl and A. W. Mackney,Chem. Rev.,64, 129 (1964); (i) R. Huisgen,J. Org. Chem.,41, 403 (1976); (j) R. A. Firestone,Tetrahedron,33, Report #39, 3009 (1977).

5. For a review of thermally generated pentagonal heterocyclic ylids, see J. Elguero;Bull. Soc. Chim. Fr., 1925 (1971).

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