Literature DB >> 19485346

A general method for the synthesis of 3,5-diarylcyclopentenones via friedel-crafts acylation of vinyl chlorides.

Yingju Xu1, Mark McLaughlin, Cheng-yi Chen, Robert A Reamer, Peter G Dormer, Ian W Davies.   

Abstract

A general approach for the synthesis of 3,5-diarylcyclopentenones was developed. Key aspects of this approach are the intramolecular Friedel-Crafts-type cyclization of vinyl chlorides and subsequent Pd-catalyzed cross-coupling reactions. The requisite vinyl chloride-bearing arylacetic acid precursors are readily available by straightforward alkylation of arylacetic acid esters and undergo cyclization to yield 3-chloro-5-aryl-2-cyclopentenones when treated with AlCl(3). The vinylogous acid chloride functionality present in these immediate products allows for further elaboration via Pd-catalyzed cross-coupling chemistry, leading to a diverse array of products.

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Year:  2009        PMID: 19485346     DOI: 10.1021/jo900696k

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  1 in total

1.  Synthesis of chamaecypanone C analogues from in situ-generated cyclopentadienones and their biological evaluation.

Authors:  Suwei Dong; Tian Qin; Ernest Hamel; John A Beutler; John A Porco
Journal:  J Am Chem Soc       Date:  2012-11-20       Impact factor: 15.419

  1 in total

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