SYNTHESIS OF CHIRAL PYRAN DERIVATIVES FROM A 3-O-ALLYLFURANOSE-5-ALDEHYDE BY THE APPLICATION OF INTRAMOLECULAR 1,3-DIPOLAR NITRILE OXIDE CYCLOADDITION

Authors
MUKHOPADHYAY R DATTA S CHATTOPADHYAY P BHATTACHARJYA A PATRA A
Citation
R. Mukhopadhyay et al., SYNTHESIS OF CHIRAL PYRAN DERIVATIVES FROM A 3-O-ALLYLFURANOSE-5-ALDEHYDE BY THE APPLICATION OF INTRAMOLECULAR 1,3-DIPOLAR NITRILE OXIDE CYCLOADDITION, Indian journal of chemistry. Sect. B: organic chemistry, including medical chemistry, 35(11), 1996, pp. 1190-1193
Citations number
11
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Indian journal of chemistry. Sect. B: organic chemistry, including medical chemistry → ACNP
ISSN journal
03764699
Volume
35
Issue
11
Year of publication
1996
Pages
1190 - 1193
Database
ISI
SICI code
0376-4699(1996)35:11<1190:SOCPDF>2.0.ZU;2-X
Abstract
The chiral pyranoisoxazoline 5 is formed as the exclusive product in t he intramolecular 1,3-dipolar nitrile oxide cycloaddition of 4 derived from the oxime of 3-O-allylfuranose-5-aldehyde 2, and is converted to the tetrasubstituted pyran 8.