DIASTEREOSELECTIVE SYNTHESIS OF (1S,2S,3R,4R) AND 3R,4S)-BICYCLO[2.2.1]HEPT-2-AMINO-2,3-DICARBOXYLIC ACIDS - NEW CONFORMATIONALLY-CONSTRAINED (S)-ASPARTIC ACID ANALOGS

Authors
BUNUEL E CATIVIELA C DIAZDEVILLEGAS MD
Citation
E. Bunuel et al., DIASTEREOSELECTIVE SYNTHESIS OF (1S,2S,3R,4R) AND 3R,4S)-BICYCLO[2.2.1]HEPT-2-AMINO-2,3-DICARBOXYLIC ACIDS - NEW CONFORMATIONALLY-CONSTRAINED (S)-ASPARTIC ACID ANALOGS, Tetrahedron : asymmetry, 7(5), 1996, pp. 1521-1528
Citations number
31
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear","Chemistry Physical
Journal title
Tetrahedron : asymmetry → ACNP
ISSN journal
09574166
Volume
7
Issue
5
Year of publication
1996
Pages
1521 - 1528
Database
ISI
SICI code
0957-4166(1996)7:5<1521:DSO(A3>2.0.ZU;2-O
Abstract
The title compounds were prepared from key intermediates readily obtai ned by the stereoselective Diels-Alder reaction of ethyl-1,3-dioxolan- 4-ylmethylene]-5(4H)-oxazolone, a chiral az-lactone derived from (R)-g lyceraldehyde and cyclopentadiene. Copyright (C) 1996 Elsevier Science Ltd