A HIGHLY STEREOSELECTIVE SYNTHESIS OF DES-A B-AROMATIC AZASTEROIDS

Authors
TREHAN IR SINGH NP JAIN VK
Citation
Ir. Trehan et al., A HIGHLY STEREOSELECTIVE SYNTHESIS OF DES-A B-AROMATIC AZASTEROIDS, Indian journal of chemistry. Sect. B: organic chemistry, including medical chemistry, 34(6), 1995, pp. 484-486
Citations number
19
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Indian journal of chemistry. Sect. B: organic chemistry, including medical chemistry → ACNP
ISSN journal
03764699
Volume
34
Issue
6
Year of publication
1995
Pages
484 - 486
Database
ISI
SICI code
0376-4699(1995)34:6<484:AHSSOD>2.0.ZU;2-8
Abstract
An efficient stereoselective synthesis of des-A B-aromatic azasteroid (5) has been achieved by intramolecular Diels-Alder reaction (IMDAR) o f the orthoquinodimethane obtained by thermolysis of xybenzocyclobuten -1-yl)methyl]-2-methylpropenamide (3).