ENANTIOSELECTIVE SYNTHESIS OF (-)-INDOLIZIDINE 239AB )-3-BUTYL-5-(3-HYDROXYPROPYL)-OCTAHYDROINDOLIZINE]

Authors
THANH GV CELERIER JP LHOMMET G
Citation
Gv. Thanh et al., ENANTIOSELECTIVE SYNTHESIS OF (-)-INDOLIZIDINE 239AB )-3-BUTYL-5-(3-HYDROXYPROPYL)-OCTAHYDROINDOLIZINE], Tetrahedron : asymmetry, 7(8), 1996, pp. 2211-2212
Citations number
11
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear","Chemistry Physical
Journal title
Tetrahedron : asymmetry → ACNP
ISSN journal
09574166
Volume
7
Issue
8
Year of publication
1996
Pages
2211 - 2212
Database
ISI
SICI code
0957-4166(1996)7:8<2211:ESO(2)>2.0.ZU;2-0
Abstract
A highly enantioselective synthesis of the indolizidine alkaloid 239AB is described via the diastereoselective reduction of a chiral cyclic beta-enamino ester prepared from (S)-pyroglutamic acid. Copyright (C) 1996 Elsevier Science Ltd