STEREOSELECTIVE SYNTHESIS OF ENANTIOPURE CYCLOPROPANE DIDEHYDROAMINO ACID-DERIVATIVES - ZYLOXYCARBONYLAMINO-4,5-CYCLOPROPANE-2-HEXENODIOIC ACID DIMETHYL ESTER

Authors
HANAFI N ORTUNO RM
Citation
N. Hanafi et Rm. Ortuno, STEREOSELECTIVE SYNTHESIS OF ENANTIOPURE CYCLOPROPANE DIDEHYDROAMINO ACID-DERIVATIVES - ZYLOXYCARBONYLAMINO-4,5-CYCLOPROPANE-2-HEXENODIOIC ACID DIMETHYL ESTER, Tetrahedron : asymmetry, 5(9), 1994, pp. 1657-1660
Citations number
17
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear","Chemistry Physical
Journal title
Tetrahedron : asymmetry → ACNP
ISSN journal
09574166
Volume
5
Issue
9
Year of publication
1994
Pages
1657 - 1660
Database
ISI
SICI code
0957-4166(1994)5:9<1657:SSOECD>2.0.ZU;2-R
Abstract
The title amino acid derivative has been synthesized stereoselectively in 40% overall yield from 5-tert-butyldiphenylsilyloxymethyl-2(5H)-fu ranone used as a chiral precursor.