1,3-dipolar cycloadditions VI. Structure and conformation of cycloadducts from reactions of C-aryl-N-phenylnitrones with substituted cinnamic acid amides

Citation
A. Banerji et al., 1,3-dipolar cycloadditions VI. Structure and conformation of cycloadducts from reactions of C-aryl-N-phenylnitrones with substituted cinnamic acid amides, MONATS CHEM, 131(8), 2000, pp. 901-911
Citations number
7
Categorie Soggetti
Chemistry
Journal title
MONATSHEFTE FUR CHEMIE
ISSN journal
00269247 → ACNP
Volume
131
Issue
8
Year of publication
2000
Pages
901 - 911
Database
ISI
SICI code
0026-9247(200008)131:8<901:1CVSAC>2.0.ZU;2-X
Abstract
Studies on cycloadditions of C,N-diarylnitrones to cinnamic acid amides wer e carried out. The diastereoisomeric (I, II) and (in some cases) regioisome ric (III) cycloadducts obtained were characterized by spectroscopic and X-r ay data. Conformational studies were carried out by molecular modelling.