INTRAMOLECULAR CYCLIZATION REACTIONS OF ENONE RADICALS

Authors
SHA CK SHEN CY JEAN TS CHIU RT TSENG WH
Citation
Ck. Sha et al., INTRAMOLECULAR CYCLIZATION REACTIONS OF ENONE RADICALS, Tetrahedron letters, 34(47), 1993, pp. 7641-7644
Citations number
11
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
34
Issue
47
Year of publication
1993
Pages
7641 - 7644
Database
ISI
SICI code
0040-4039(1993)34:47<7641:ICROER>2.0.ZU;2-R
Abstract
Enone radicals, generated from the corresponding iodo enones, or vinyl ogous esters and amides, undergo intramolecular cyclization to the tet hered trimethylsilyl acetylenic side chain to give the carbo- or heter obicyclic enones.