Mesoionic compounds. 10. Preferred conformation of a 3-alkyl and 3-aryl-substituent in 4-unsubstituted and 4-acylated monocyclic munchnones and sydnones

Citation
H. Petride et al., Mesoionic compounds. 10. Preferred conformation of a 3-alkyl and 3-aryl-substituent in 4-unsubstituted and 4-acylated monocyclic munchnones and sydnones, REV RO CHIM, 44(3), 1999, pp. 249-259
Citations number
36
Categorie Soggetti
Chemistry
Journal title
REVUE ROUMAINE DE CHIMIE
ISSN journal
00353930 → ACNP
Volume
44
Issue
3
Year of publication
1999
Pages
249 - 259
Database
ISI
SICI code
0035-3930(199903)44:3<249:MC1PCO>2.0.ZU;2-K
Abstract
A new 4-unsubstituted monocyclic oxazolium-5-olate (7c) was generated and N MR-characterized. Several 3-alkyl- and 3-aryl-4-acylated monocyclic munchno ne and sydnone derivatives were also prepared. From NMR experimental data a nd theoretical calculations different conformations were proposed for the 3 -alkyl group in munchnone- and sydnone series. The 3-arylated mesoionic oxa zolones presented non-planar structures.