K. Shioji, Aya Tashiro, Sanae Shibata
Jan 27, 2003
Citations
0
Influential Citations
23
Citations
Journal
Tetrahedron Letters
Abstract
Abstract Lipase-catalyzed acylation of ethyl (1-hydroxyalkyl)phenylphosphinates afforded a single diastereomer in high enantiomeric excess. The substituent effect of the alkyl group toward the acylation using Candida antractica (CAL) was larger than that of an immobilized lipase from Pseudomonas fluorescens lipase (lipase AK).