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Sequential acyl halide-aldehyde cyclocondensation and enzymatic resolution as a route to enantiomerically enriched beta-lactones

Authors :
Nelson, Scott G.
Spencer, Keith L.
Source :
Journal of Organic Chemistry. Feb 25, 2000, Vol. 65 Issue 4, p1227, 4 p.
Publication Year :
2000

Abstract

Research has been conducted on the beta-lactones. The preparation of the optically active beta-lactones via enzymatic resolution of the racemic 4-substituted-2-oxetanones derived from the acyl halide-aldehyde reactions has been investigated.

Details

ISSN :
00223263
Volume :
65
Issue :
4
Database :
Gale General OneFile
Journal :
Journal of Organic Chemistry
Publication Type :
Academic Journal
Accession number :
edsgcl.77706989