A NEW DIASTEREOSELECTIVE ROUTE TO 5-SUBSTITUTED-8-METHYLINDOLIZIDINES- SYNTHESIS OF INDOLIZIDINE-(-)-209B

Authors
BARDOU A CELERIER JP LHOMMET G
Citation
A. Bardou et al., A NEW DIASTEREOSELECTIVE ROUTE TO 5-SUBSTITUTED-8-METHYLINDOLIZIDINES- SYNTHESIS OF INDOLIZIDINE-(-)-209B, Tetrahedron letters, 39(29), 1998, pp. 5189-5192
Citations number
21
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
39
Issue
29
Year of publication
1998
Pages
5189 - 5192
Database
ISI
SICI code
0040-4039(1998)39:29<5189:ANDRT5>2.0.ZU;2-P
Abstract
The highly diastereoselective synthesis of the indolizidine alkaloid ( -) 209B is described via the diastereoselective alkylation of a chiral cyclic beta-amino ester prepared from (R)-methylbenzylamine. (C) 1998 Published by Elsevier Science Ltd. All rights reserved.