Issue 104, 2014

An odorless, one-pot synthesis of nitroaryl thioethers via SNAr reactions through the in situ generation of S-alkylisothiouronium salts

Abstract

A newly developed C–S bond formation nucleophilic aromatic substitution (SNAr) reaction in aqueous Triton X-100 (TX100) micelles has been disclosed. This chemistry, in which odorless, cheap and stable thiourea in place of thiols is used as the sulfur reagent, provides an efficient approach for the generation of nitroaryl thioethers, which are useful structural units of many bioactive molecules, rendering this methodology attractive to both synthetic and medicinal chemistry.

Graphical abstract: An odorless, one-pot synthesis of nitroaryl thioethers via SNAr reactions through the in situ generation of S-alkylisothiouronium salts

Supplementary files

Article information

Article type
Paper
Submitted
30 Sep 2014
Accepted
28 Oct 2014
First published
28 Oct 2014

RSC Adv., 2014,4, 59990-59996

Author version available

An odorless, one-pot synthesis of nitroaryl thioethers via SNAr reactions through the in situ generation of S-alkylisothiouronium salts

G. Lu and C. Cai, RSC Adv., 2014, 4, 59990 DOI: 10.1039/C4RA11490F

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