| Literature DB >> 12707813 |
A-S Bessis1, G Vadesne, E Bourrat, G Bertho, J-P Pin, F C Acher.
Abstract
Two glutamic acid analogs (1 SR,3 RS,4 RS)- and (1 SR,3 SR,4 SR)-1-amino-4-phosphono cyclopentane-1,3-dicarboxylic acids (APCPD) have been synthesized. Pure E-(diethoxy-phosphoryl)-acrylic acid ethyl ester was obtained from ethyl propiolate, phenol and triethylphosphite. It was used as dienophile in a Diels-Alder reaction. Oxidation and cyclization afforded 3-(ethoxy-carbonyl)-4-(diethoxy-phosphoryl)-cyclopentanone. Bucherer-Bergs reaction and hydrolysis yielded APCPD-III and -IV which are inactive on mGlu1a receptor and antagonists on mGlu2 and mGlu8a receptors.Entities:
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Year: 2003 PMID: 12707813 DOI: 10.1007/s00726-002-0405-6
Source DB: PubMed Journal: Amino Acids ISSN: 0939-4451 Impact factor: 3.520