Literature DB >> 18095699

A convergent synthesis of the tricyclic core of the dictyosphaeric acids.

Christopher W Barfoot1, Alan R Burns, Michael G Edwards, Martin N Kenworthy, Mahmood Ahmed, Stephen E Shanahan, Richard J K Taylor.   

Abstract

The first synthetic route to the tricyclic core of the dictyosphaeric acids has been established starting from readily available (S)-(-)-4-(tert-butyldimethylsilyloxy)cyclohexenone and involving 9 steps, including a ring-closing metathesis to produce a 13-membered macrolactone, and a doubly tethered intramolecular Michael addition.

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Year:  2007        PMID: 18095699     DOI: 10.1021/ol702887e

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  1 in total

1.  Asymmetric [4+2] cycloadditions employing 1,3-dienes derived from (R)-4-t-butyldimethyl-silyloxy-2-cyclohexen-1-one.

Authors:  Zhengmao Hua; Lei Chen; Yan Mei; Zhendong Jin
Journal:  Tetrahedron Lett       Date:  2009-12-01       Impact factor: 2.415

  1 in total

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