ENANTIOSELECTIVE AND DIASTEREOSELECTIVE SYNTHESIS OF ISOXAZOLIDINES BY ASYMMETRIC 1,3-DIPOLAR CYCLOADDITION OF NITRONES

Authors
UKAJI Y TANIGUCHI K SADA K INOMATA K
Citation
Y. Ukaji et al., ENANTIOSELECTIVE AND DIASTEREOSELECTIVE SYNTHESIS OF ISOXAZOLIDINES BY ASYMMETRIC 1,3-DIPOLAR CYCLOADDITION OF NITRONES, Chemistry Letters, (6), 1997, pp. 547-548
Citations number
17
Categorie Soggetti
Chemistry
Journal title
Chemistry Letters → ACNP
ISSN journal
03667022
Issue
6
Year of publication
1997
Pages
547 - 548
Database
ISI
SICI code
0366-7022(1997):6<547:EADSOI>2.0.ZU;2-T
Abstract
The asymmetric 1,3-dipolar cycloaddition of nitrones possessing electr on withdrawing group to an achiral allyl alcohol was achieved by the u se of diisopropyl (R,R)-tartrate as a chiral auxiliary to afford the c orresponding isoxazolidines with high regio-, diastereo- and enantiose lectivity.