Literature DB >> 23252990

Asymmetric synthesis of α-alkylidene-β-hydroxy-γ-butyrolactones via enantioselective tandem Michael-aldol reaction.

Sung Il Lee1, Jin Hee Jang, Geum-Sook Hwang, Do Hyun Ryu.   

Abstract

A simple and efficient method for the asymmetric synthesis of α-alkylidene-β-hydroxy-γ-butyrolactones and related natural products was developed on the basis of the catalytic asymmetric tandem Michael-aldol reaction and simple transformations. The synthetic utility of this method was illustrated by the facile synthesis of trisubstituted γ-butyrolactone natural products.

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Year:  2012        PMID: 23252990     DOI: 10.1021/jo302369q

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


  1 in total

1.  Lewis Acid-Promoted Enantioselective Dearomative Spirocyclizations of Allenes.

Authors:  Sergei Tcyrulnikov; John M Curto; Philip H Gilmartin; Marisa C Kozlowski
Journal:  J Org Chem       Date:  2018-09-05       Impact factor: 4.354

  1 in total

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