Issue 11, 1996
From the journal:

Chemical Communications

A facile route to (+)- and (–)-trans-tetrahydro-5-oxo-2-pentylfuran-3-carboxylic acid, precursors of (+)- and (–)-methylenolactocin

Sara Drioli,   Fulvia Felluga,   Cristina Forzato,   Patrizia Nitti  and  Giuliana Pitacco  

Abstract

The enantioselective synthesis of the title γ-lactone intermediates is easily achieved by employing Porcine pancreas lipase catalysed hydrolysis of the corresponding esters as the key step.

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Article information

DOI
https://doi.org/10.1039/CC9960001289
Article type
Paper

Chem. Commun., 1996, 1289-1290

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A facile route to (+)- and (–)-trans-tetrahydro-5-oxo-2-pentylfuran-3-carboxylic acid, precursors of (+)- and (–)-methylenolactocin

S. Drioli, F. Felluga, C. Forzato, P. Nitti and G. Pitacco, Chem. Commun., 1996, 1289 DOI: 10.1039/CC9960001289

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