STEREOCONTROLLED SYNTHESES OF POLYHYDROXY INDOLIZIDINES, INCLUDING 8A-EPI-CASTANOSPERMINE, 6,8A-DIEPI-CASTANOSPERMINE AND 1,6-DIEPI-CASTANOSPERMINE, STARTING FROM MALIC-ACID

Authors
LEEPER FJ HOWARD S
Citation
Fj. Leeper et S. Howard, STEREOCONTROLLED SYNTHESES OF POLYHYDROXY INDOLIZIDINES, INCLUDING 8A-EPI-CASTANOSPERMINE, 6,8A-DIEPI-CASTANOSPERMINE AND 1,6-DIEPI-CASTANOSPERMINE, STARTING FROM MALIC-ACID, Tetrahedron letters, 36(13), 1995, pp. 2335-2338
Citations number
23
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
36
Issue
13
Year of publication
1995
Pages
2335 - 2338
Database
ISI
SICI code
0040-4039(1995)36:13<2335:SSOPII>2.0.ZU;2-G
Abstract
Stereocontrolled total syntheses of one trihydroxy indolizidine 15 and three tetrahydroxy indolizidines, 17, 21 and 23 - all diastereoisomer s of castanospermine - are described which use malic acid as the only chiral starting material.