Literature DB >> 30449906

A stereoselective synthesis of (+)-boronolide.

Arun K Ghosh1, Geoffrey Bilcer1.   

Abstract

A stereoselective synthesis of (+)-boronolide is described. The key steps involve a stereoselective reduction of an α-hydroxy ketone, allylation of an α-hydroxy aldehyde and a ring-closing olefin metathesis of a homoallylic alcohol derived acrylate ester utilizing Grubbs' catalyst.

Entities:  

Year:  2000        PMID: 30449906      PMCID: PMC6234978          DOI: 10.1016/S0040-4039(99)02246-7

Source DB:  PubMed          Journal:  Tetrahedron Lett        ISSN: 0040-4039            Impact factor:   2.415


  1 in total

1.  Synthesis of gem-difluoromethylenated analogues of boronolide.

Authors:  Jing Lin; Xiao-Long Qiu; Feng-Ling Qing
Journal:  Beilstein J Org Chem       Date:  2010-04-20       Impact factor: 2.883

  1 in total

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