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Issue 3, 2012
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Oxidative cross-esterification of dithiolanes with alcohols through a cross-dehydrogenative coupling (CDC)/deprotection sequence

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Abstract

An unprecedented oxidative cross-esterification in an equimolar mixture of dithiolanes, alcohols and water through a CDC/deprotection sequence has been developed. The reaction itself features simple experimental procedures under very mild conditions and offers a new strategic protocol for the direct and efficient synthesis of structurally diverse esters.

Graphical abstract: Oxidative cross-esterification of dithiolanes with alcohols through a cross-dehydrogenative coupling (CDC)/deprotection sequence

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Article information


Submitted
08 Oct 2011
Accepted
09 Nov 2011
First published
28 Nov 2011

Org. Biomol. Chem., 2012,10, 506-508
Article type
Communication

Oxidative cross-esterification of dithiolanes with alcohols through a cross-dehydrogenative coupling (CDC)/deprotection sequence

L. Fu, C. Yao, N. Chang, J. Chen, L. Lu and W. Xiao, Org. Biomol. Chem., 2012, 10, 506
DOI: 10.1039/C1OB06890C

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