Literature DB >> 17311391

Synthesis of the fused polyether core of hemibrevetoxin B by two-directional ring-closing metathesis.

J Stephen Clark1, Damian M Grainger, Alexandra A-C Ehkirch, Alexander J Blake, Claire Wilson.   

Abstract

The tetracyclic fused polyether core of the marine natural product hemibrevetoxin B has been prepared in an efficient manner by using a strategy in which ring-closing metathesis (RCM) reactions were employed for ring synthesis. Simultaneous construction of the A and D rings was accomplished by double two-directional RCM of a tetraene. [reaction: see text]

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Year:  2007        PMID: 17311391     DOI: 10.1021/ol0630651

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


  1 in total

1.  Stereoselective Synthesis of the I-L Fragment of the Pacific Ciguatoxins.

Authors:  J Stephen Clark; Michael Popadynec
Journal:  Toxins (Basel)       Date:  2020-11-24       Impact factor: 4.546

  1 in total

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