ASYMMETRIC-SYNTHESIS OF DIFFERENTIALLY PROTECTED 2,7-DIAMINOSUBERIC ACID, A RING-CLOSURE METATHESIS APPROACH

Citation
Rm. Williams et Jw. Liu, ASYMMETRIC-SYNTHESIS OF DIFFERENTIALLY PROTECTED 2,7-DIAMINOSUBERIC ACID, A RING-CLOSURE METATHESIS APPROACH, Journal of organic chemistry, 63(7), 1998, pp. 2130-2132
Citations number
13
Language
INGLESE
art.tipo
Article
Categorie Soggetti
Chemistry Inorganic & Nuclear
ISSN journal
0022-3263
Volume
63
Issue
7
Year of publication
1998
Pages
2130 - 2132
Database
ISI
SICI code
0022-3263(1998)63:7<2130:AODP2A>2.0.ZU;2-Q
Abstract
An efficient and versatile method has been developed for the synthesis of a selectively protected 2,7-diaminosuberic acid derivative. A Grub bs ring-closure olefin metathesis reaction was used as a key step on a n allylglycine-derived template.