| Literature DB >> 20420378 |
Zhongyu Duan1, Sadananda Ranjit, Xiaogang Liu.
Abstract
A series of amine-substituted aryl sulfides have been synthesized from nitroaryl halides via a simple one-pot procedure involving metal-free C-S cross-coupling and in situ nitro group reduction. Various nitroaryl halides were reacted with thiols in recyclable poly(ethylene glycol) to afford the amine-substituted aryl sulfides in high yield. Additionally, the cross-coupling reactions of nitro- and aldehyde-substituted aryl halides with benzyl thiols under the same reaction conditions were demonstrated to afford benzothiazole and phenylbenzo[b]thiophene derivatives.Entities:
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Year: 2010 PMID: 20420378 DOI: 10.1021/ol100816g
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005