Issue 3, 2012
From the journal:

Organic & Biomolecular Chemistry

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

Liang Fu,a   Chang-Jiang Yao,a   Ning-Jie Chang,a   Jia-Rong Chen,a   Liang-Qiu Lu*a  and  Wen-Jing Xiao*a  

* Corresponding authors

a Key Laboratory of Pesticide & Chemical Biology, Ministry of Education, College of Chemistry, Central China Normal University, 152 Luoyu Road, Wuhan, Hubei 430079, China
E-mail: wxiao@mail.ccnu.edu.cn

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

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C1OB06890C
Article type
Communication
Submitted
08 Oct 2011
Accepted
09 Nov 2011
First published
28 Nov 2011

Org. Biomol. Chem., 2012,10, 506-508

Permissions

Request permissions

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

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.

Social activity

Spotlight

Advertisements