| Literature DB >> 28333469 |
Subramani Sangeetha1, Govindasamy Sekar1.
Abstract
An efficient protocol is described for the synthesis of 2-acylbenzo[b]thiophenes from easily accessible 2-iodochalcones through α-C-H functionalization using Cu(OAc)2 catalyst and xanthate as sulfur source. Less reactive 2-bromochalcones also yielded the corresponding 2-acylbenzothiophenes in good yield. The reaction proceeds via in situ incorporation of sulfur followed by copper-catalyzed cyclization to generate 2-acylbenzothiophenes without external acyl source. The synthetic importance is showcased by synthesis of 1-(5-hydroxybenzothiophene-2-yl)ethanone, which is a known pre-mRNA splicing modulator.Entities:
Year: 2017 PMID: 28333469 DOI: 10.1021/acs.orglett.7b00462
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005