AN EXPEDITIOUS ENANTIODIVERGENT SYNTHESIS OF CHIRAL OXEPANES FROM D-GLUCOSE BY THE APPLICATION OF INTRAMOLECULAR 1,3-DIPOLAR NITRONE CYCLOADDITION

Authors
DATTA S CHATTOPADHYAY P MUKHOPADHYAY R BHATTACHARJYA A
Citation
S. Datta et al., AN EXPEDITIOUS ENANTIODIVERGENT SYNTHESIS OF CHIRAL OXEPANES FROM D-GLUCOSE BY THE APPLICATION OF INTRAMOLECULAR 1,3-DIPOLAR NITRONE CYCLOADDITION, Tetrahedron letters, 34(22), 1993, pp. 3585-3588
Citations number
6
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
34
Issue
22
Year of publication
1993
Pages
3585 - 3588
Database
ISI
SICI code
0040-4039(1993)34:22<3585:AEESOC>2.0.ZU;2-5
Abstract
The enantiomers of an oxepanoisoxazolidine and a chiral oxepane, poten tially useful as precursors for naturally occurring oxepanes, were syn thesised from D-glucose involving Intramolecular 1,3-dipolar nitrone c ycloaddition.