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

Liang Fu; Chang Jiang Yao; Ning Jie Chang; Jia Rong Chen; Liang Qiu Lu; Wen Jing Xiao

doi:10.1039/c1ob06890c

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

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

^*Corresponding author for this work

Central China Normal University

Research output: Contribution to journal › Article › peer-review

15 Citations (Scopus)

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.

Original language	English
Pages (from-to)	506-508
Number of pages	3
Journal	Organic and Biomolecular Chemistry
Volume	10
Issue number	3
DOIs	https://doi.org/10.1039/c1ob06890c
Publication status	Published - 21 Jan 2012
Externally published	Yes

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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.",

author = "Liang Fu and Yao, {Chang Jiang} and Chang, {Ning Jie} and Chen, {Jia Rong} and Lu, {Liang Qiu} and Xiao, {Wen Jing}",

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AU - Fu, Liang

AU - Yao, Chang Jiang

AU - Chang, Ning Jie

AU - Chen, Jia Rong

AU - Lu, Liang Qiu

AU - Xiao, Wen Jing

PY - 2012/1/21

Y1 - 2012/1/21

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AB - 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.

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DO - 10.1039/c1ob06890c

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AN - SCOPUS:84055178579

SN - 1477-0520

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SP - 506

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JF - Organic and Biomolecular Chemistry

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

Abstract

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