Issue 67, 2016

Copper and triphenylphosphine-promoted sulfenylation of quinones with arylsulfonyl chlorides

Abstract

The efficient copper and triphenylphosphine-promoted sulfenylation of quinones with arylsulfonyl chlorides has been developed under mild conditions with moderate to good yields. Significantly, this provides an alternative method to synthesise arylthioquinone derivatives. This is the first time that arylthioquinones with arylsulfonyl chlorides as starting material have been prepared, which avoids the use of the awful smelling thioalcohols and thiophenols.

Graphical abstract: Copper and triphenylphosphine-promoted sulfenylation of quinones with arylsulfonyl chlorides

Supplementary files

Article information

Article type
Communication
Submitted
02 Mot 2016
Accepted
21 Jan 2016
First published
23 Jan 2016

RSC Adv., 2016,6, 62298-62301

Copper and triphenylphosphine-promoted sulfenylation of quinones with arylsulfonyl chlorides

X. Yu, Q. Wu, H. Wan, Z. Xu, X. Xu and D. Wang, RSC Adv., 2016, 6, 62298 DOI: 10.1039/C6RA11301J

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