Literature DB >> 14770242

Total synthesis of (+)-tanikolide via oxidative lactonization.

Jennifer M Schomaker1, Babak Borhan.   

Abstract

(+)-Tanikolide has been synthesized in eight linear steps with a 31% overall yield. The key step in the synthesis utilizes a recently developed tandem oxidative cleavage-lactonization of a precursor alkenol to deliver the lactone moiety.

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Year:  2004        PMID: 14770242     DOI: 10.1039/b311432e

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  2 in total

1.  Structural and synthetic investigations of tanikolide dimer, a SIRT2 selective inhibitor, and tanikolide seco-acid from the Madagascar marine cyanobacterium Lyngbya majuscula.

Authors:  Marcelino Gutiérrez; Eric H Andrianasolo; Won Kyo Shin; Douglas E Goeger; Alexandre Yokochi; Jörg Schemies; Manfred Jung; Dennis France; Susan Cornell-Kennon; Eun Lee; William H Gerwick
Journal:  J Org Chem       Date:  2009-08-07       Impact factor: 4.354

Review 2.  Chemical compounds toxic to invertebrates isolated from marine cyanobacteria of potential relevance to the agricultural industry.

Authors:  Magbubah Essack; Hanin S Alzubaidy; Vladimir B Bajic; John A C Archer
Journal:  Toxins (Basel)       Date:  2014-10-29       Impact factor: 4.546

  2 in total

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