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Determination of the absolute configuration and solution conformation of a novel disubstituted pyrrolidine acid A by vibrational circular dichroism.

Authors :
Freedman TB
Cao X
Phillips LM
Cheng PT
Dalterio R
Shu YZ
Zhang H
Zhao N
Shukla RB
Tymiak A
Gozo SK
Nafie LA
Gougoutas JZ
Source :
Chirality [Chirality] 2006 Sep; Vol. 18 (9), pp. 746-53.
Publication Year :
2006

Abstract

Compound A, a novel disubstituted pyrrolidine acid, is a member of a new class of agents that are potentially useful for the treatment of diabetes and dyslipidemia. The absolute configuration of this compound was determined by using vibrational circular dichroism (VCD). The results are in agreement with the assignments based on both X-ray analysis and the stereo-selective chemical synthesis. During VCD analysis, the solution conformation for a portion of compound A in CDCl(3) was also established. The compound is found to associate as an H-bonded carboxylic acid "dimer" in CDCl(3) solution, and VCD calculations on a model dimer fragment were required to establish the absolute configuration.

Details

Language :
English
ISSN :
0899-0042
Volume :
18
Issue :
9
Database :
MEDLINE
Journal :
Chirality
Publication Type :
Academic Journal
Accession number :
16856170
Full Text :
https://doi.org/10.1002/chir.20316