Literature DB >> 12509898

Synthesis of the carbocyclic core of the cornexistins by ring-closing metathesis.

J Stephen Clark1, Frederic Marlin, Bastien Nay, Claire Wilson.   

Abstract

An advanced intermediate in the synthesis of the phytotoxins cornexistin and hydroxycornexistin has been synthesized. Sequential palladium-mediated sp(2)-sp(3) fragment coupling and ring-closing diene metathesis have been used to construct the nine-membered carbocyclic core found in the natural products. [reaction--see text]

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Year:  2003        PMID: 12509898     DOI: 10.1021/ol027265y

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


  2 in total

1.  Novel route to 5-position vinyl derivatives of thiolactomycin: Olefination vs. deformylation.

Authors:  Pilho Kim; Clifton E Barry; Cynthia S Dowd
Journal:  Tetrahedron Lett       Date:  2006-05-15       Impact factor: 2.415

2.  9-Membered Carbocycles: Strategies and Tactics for their Synthesis.

Authors:  Tatjana Huber; Raphael E Wildermuth; Thomas Magauer
Journal:  Chemistry       Date:  2018-03-13       Impact factor: 5.236

  2 in total

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