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Molecules. 2012 Dec 21;18(1):50-73. doi: 10.3390/molecules18010050.

Synthesis of new optically active 2-pyrrolidinones.

Author information

1
Laboratory of Organic Chemistry, Department of Chemistry, University of Athens, Panepistimiopolis, Athens, Greece. pminakak@chem.uoa.gr

Abstract

A new class of optically active 2-pyrrolidinones was synthesized, starting from S-pyroglutamic acid, a well known natural chiral synthon. The synthetic design followed led to the insertion of various substituents at positions 1 and 5 of the 2-pyrrolidinone ring, including the imidazole moiety. Some of them possess two or three stereogenic centers, the configuration of which was retained under the mild conditions used. The new compounds also carry an imidazole moiety, which, along with the 2-pyrrolidinone template, may prove pivotal to several biological processes.

PMID:
23344188
DOI:
10.3390/molecules18010050
[Indexed for MEDLINE]
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