Issue 20, 2010

Confirmation by IR of the preferred conformations of CFTAesters in solution: a highly reliable criterion for the stereochemistry assignment of chiral alcohols

Abstract

Direct confirmation of the preferred conformation of diastereomeric esters derived from a chiral secondary alcohol and a chiral derivatizing agent in solution, which is crucial for reliable NMR-based assignment of absolute stereochemistry of the alcohol, has been attained for the first time by examination of IR spectra of the CFTA esters.

Graphical abstract: Confirmation by IR of the preferred conformations of CFTA esters in solution: a highly reliable criterion for the stereochemistry assignment of chiral alcohols

Supplementary files

Article information

Article type
Communication
Submitted
21 Dec 2009
Accepted
19 Mar 2010
First published
15 Apr 2010

Chem. Commun., 2010,46, 3610-3612

Confirmation by IR of the preferred conformations of CFTA esters in solution: a highly reliable criterion for the stereochemistry assignment of chiral alcohols

K. Omata, K. Kotani, K. Kabuto, T. Fujiwara and Y. Takeuchi, Chem. Commun., 2010, 46, 3610 DOI: 10.1039/B926793J

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