Literature DB >> 28333469

Synthesis of 2-Acylbenzo[b]thiophenes via Cu-Catalyzed α-C-H Functionalization of 2-Halochalcones Using Xanthate.

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


  2 in total

1.  The reaction of potassium xanthates with five-membered cyclic carbonates: selectivity of the underlying cascade reactions and mechanistic insights.

Authors:  Misha Rumyantsev; Ilia A Korablev; Sergey Rumyantsev
Journal:  RSC Adv       Date:  2020-10-01       Impact factor: 3.361

2.  Crystal structures of 2-(2-bromo-5-fluoro-phen-yl)-8-eth-oxy-3-nitro-2H-thio-chromene and 2-(2-bromo-5-fluoro-phen-yl)-7-meth-oxy-3-nitro-2H-thio-chromene.

Authors:  Chien Thang Pham; Dinh Hung Mac; Thai Thanh Thu Bui
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2019-10-31
  2 in total

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