Issue 7, 1987

Enzymatic hydrolysis of 3,7-diacetoxycloheptene derivatives

Abstract

Hydrolysis of 3,7-diacetoxycycloheptene using electric eel acetylcholinesterase gives optically pure (3R,7S)-3-hydroxy-7-acetoxycycloheptene, and hydrolysis using lipase enzyme from Candida cyclindracea gives the same hydroxy acetate, but in only 44% enantiomeric excess, in contrast to the normal behaviour of lipase which gives (S) alcohols for related hydrolyses; 3,7-diacetoxy-4,6-dimethylcycloheptene (10) is not hydrolysed by acetylcholinesterase, but is readily hydrolysed by lipase to give (3S,4R,6S,7R)-3-hydroxy-7-acetoxy-4,6-dimethylcycloheptene.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1987, 519-520

Enzymatic hydrolysis of 3,7-diacetoxycloheptene derivatives

A. J. Pearson, H. S. Bansal and Y. Lai, J. Chem. Soc., Chem. Commun., 1987, 519 DOI: 10.1039/C39870000519

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements