Literature DB >> 17465560

Rapid synthesis of the A-E fragment of ciguatoxin CTX3C.

J Stephen Clark1, Joanne Conroy, Alexander J Blake.   

Abstract

The A-E fragment of the marine natural product CTX3C has been prepared in an efficient manner by using a strategy in which two-directional and iterative ring-closing metathesis (RCM) reactions were employed for ring construction.

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Year:  2007        PMID： 17465560     DOI： 10.1021/ol0706096

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


  3 in total

1.  Concise synthesis of the A/BCD-ring fragment of gambieric acid A.

Authors:  Haruhiko Fuwa; Ryo Fukazawa; Makoto Sasaki
Journal:  Front Chem       Date:  2015-01-13       Impact factor: 5.221

2.  Bidirectional Synthesis of the IJK Fragment of Ciguatoxin CTX3C by Sequential Double Ring-Closing Metathesis and Tsuji-Trost Allylation.

Authors:  Michael Popadynec; Helen Gibbard; J Stephen Clark
Journal:  Org Lett       Date:  2020-04-19       Impact factor: 6.005

3.  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
  3 in total

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