SPIROLACTAMS BY A NOVEL IPSO-RADICAL CYCLIZATION AND LOSS OF AROMATICITY

Authors
BOIVIN J YOUSFI M ZARD SZ
Citation
J. Boivin et al., SPIROLACTAMS BY A NOVEL IPSO-RADICAL CYCLIZATION AND LOSS OF AROMATICITY, Tetrahedron letters, 38(34), 1997, pp. 5985-5988
Citations number
24
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
38
Issue
34
Year of publication
1997
Pages
5985 - 5988
Database
ISI
SICI code
0040-4039(1997)38:34<5985:SBANIC>2.0.ZU;2-P
Abstract
Spirolactams are obtained by ipso radical cyclisation when various sub stituted N-benzyl trichloroacetamides are subjected to the nickel powd er/acetic acid reducing system. (C) 1997 Elsevier Science Ltd.