DIASTEREOSELECTIVE SYNTHESIS OF (2S,5S)-HYDROXYHOMOPIPECOLIC AND (2R,5S)-5-HYDROXYHOMOPIPECOLIC ACID FROM S-GLUTAMIC ACID - AN ENTRY TO STREPTOLUTINE STEREOISOMERS

Authors
HERDEIS C HELD WA KIRFEL A SCHWABENLANDER F
Citation
C. Herdeis et al., DIASTEREOSELECTIVE SYNTHESIS OF (2S,5S)-HYDROXYHOMOPIPECOLIC AND (2R,5S)-5-HYDROXYHOMOPIPECOLIC ACID FROM S-GLUTAMIC ACID - AN ENTRY TO STREPTOLUTINE STEREOISOMERS, Tetrahedron, 52(18), 1996, pp. 6409-6420
Citations number
22
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron → ACNP
ISSN journal
00404020
Volume
52
Issue
18
Year of publication
1996
Pages
6409 - 6420
Database
ISI
SICI code
0040-4020(1996)52:18<6409:DSO(A(>2.0.ZU;2-A
Abstract
Starting from readily available methyl (2RS,5S) ylsilyloxy)-2-(2'-prop enyl)-piperidine-carboxylate (1), a diastereoselective synthesis of ho mopipecolic acids 5a and 5b and of di-epistreptolutine derivative 10 i s decribed. Copyright (C) 1996 Elsevier Science Ltd