AN EFFICIENT CONVERSION OF CHIRAL ALPHA-AMINO-ACIDS TO ENANTIOMERICALLY PURE 3-AMINO CYCLIC AMINES

Authors
Citation
Sh. Moon et S. Lee, AN EFFICIENT CONVERSION OF CHIRAL ALPHA-AMINO-ACIDS TO ENANTIOMERICALLY PURE 3-AMINO CYCLIC AMINES, Synthetic communications, 28(21), 1998, pp. 3919-3926
Citations number
14
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00397911
Volume
28
Issue
21
Year of publication
1998
Pages
3919 - 3926
Database
ISI
SICI code
0039-7911(1998)28:21<3919:AECOCA>2.0.ZU;2-7
Abstract
Enantiomerically pure 3-amino cyclic amines such as 3-amino pyrrolidin e, 3-amino piperidine, and 2.,3,4,5,6,7-hexahydro-1H-azepine have been synthesized in high yields from the optically active natural a-amino acids such as L-aspartic acid, L-glutamic acid, L-2-aminoadipic acid, and their enantiomers.