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Enantioselective hydrolysis of cyclic carbonates by porcine pancreatic lipase to afford optically active 1,2-alkanediols

✍ Scribed by Masatoshi Kawashima; Yuko Horikawa

Publisher: Springer Netherlands
Year: 1993
Tongue: English
Weight: 173 KB
Volume: 15
Category: Article
ISSN: 0141-5492
DOI: 10.1007/bf00129934

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✦ Synopsis

Cyclic carbonates, 1,3-dioxolan-2-ones were enantioselectlvely hydrolyzed by porcine pancreatic lipase to give optically active 1,2alkanediols.

1989).

Recently, authors have been revealed usefullness of resolution of alcohols through the carbonates by lipase-catalyzed enantioselective hydrolysis (Kawashima and.

In this paper, we

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