HIGHLY DIASTEREOMER SELECTIVE ACYLATION OF 2,5-DIALKYLPYRROLIDINES - A VERSATILE ROUTE TO TRANS-2,5-DISUBSTITUTED CYCLIC AMINO-ALCOHOLS

Authors
FLEURANT A GRANDJEAN C PROVOT O ROSSET S CELERIER JP LHOMMET G
Citation
A. Fleurant et al., HIGHLY DIASTEREOMER SELECTIVE ACYLATION OF 2,5-DIALKYLPYRROLIDINES - A VERSATILE ROUTE TO TRANS-2,5-DISUBSTITUTED CYCLIC AMINO-ALCOHOLS, Heterocycles, 36(5), 1993, pp. 929-932
Citations number
9
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Heterocycles → ACNP
ISSN journal
03855414
Volume
36
Issue
5
Year of publication
1993
Pages
929 - 932
Database
ISI
SICI code
0385-5414(1993)36:5<929:HDSAO2>2.0.ZU;2-W
Abstract
Diastereoisomeric mixtures of cis- and trans- disubstituted pyrrolidin es are separated by kinetically controlled acylation with benzyl chlor oformate.