Literature DB >> 20066276

Effect of the allylic substituents on ring closing metathesis: the total synthesis of stagonolide B and 4-epi-stagonolide B.

Awadut G Giri1, Mohabul A Mondal, Vedavati G Puranik, Chepuri V Ramana.   

Abstract

The total syntheses of stagonolide B and its 4-epimer were carried out to probe into how the relative stereochemistry of allylic hydroxy groups and their protecting groups influence the efficiency of the ring closing metathesis.

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Year:  2009        PMID： 20066276     DOI： 10.1039/b916198h

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


  3 in total

1.  Enantioselective synthesis of (Z)-1,2-anti-2,5-anti-triol monosilyl ethers using a cross-metathesis allylboration sequence.

Authors:  SusAnn M Winbush; William R Roush
Journal:  Org Lett       Date:  2010-10-01       Impact factor: 6.005

2.  The Role of Total Synthesis in Structure Revision and Elucidation of Decanolides (Nonanolides).

Authors:  Bernd Schmidt
Journal:  Prog Chem Org Nat Prod       Date:  2021

3.  Xyolide, a bioactive nonenolide from an Amazonian endophytic fungus, Xylaria feejeensis.

Authors:  Ezra G Baraban; Jesse B Morin; Gillian M Phillips; Andrew J Phillips; Scott A Strobel; Jo Handelsman
Journal:  Tetrahedron Lett       Date:  2013-07-31       Impact factor: 2.415
  3 in total

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