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

16 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

Access to Document

10.1039/c1ob06890c

Cite this

@article{3961635b45fe4749b1b8bfb529ea6984,

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

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\}",

year = "2012",

month = jan,

day = "21",

doi = "10.1039/c1ob06890c",

language = "English",

volume = "10",

pages = "506--508",

journal = "Organic and Biomolecular Chemistry",

issn = "1477-0520",

publisher = "Royal Society of Chemistry",

number = "3",

}

TY - JOUR

T1 - Oxidative cross-esterification of dithiolanes with alcohols through a cross-dehydrogenative coupling (CDC)/deprotection sequence

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

N2 - 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.

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.

UR - https://www.scopus.com/pages/publications/84055178579

U2 - 10.1039/c1ob06890c

DO - 10.1039/c1ob06890c

M3 - Article

C2 - 22120891

AN - SCOPUS:84055178579

SN - 1477-0520

VL - 10

SP - 506

EP - 508

JO - Organic and Biomolecular Chemistry

JF - Organic and Biomolecular Chemistry

IS - 3

ER -

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

Abstract

Access to Document

Other files and links

Fingerprint

Cite this