Literature DB >> 15704890

The Stille reaction in the synthesis of carotenoid butenolides: synthesis of 6'-epi-peridinin.

Belén Vaz1, Rosana Alvarez, Reinhard Brückner, Angel R de Lera.   

Abstract

A new strategy for carotenoid butenolides has been developed that is based in part in halogen-selective Stille cross-coupling of dihalogenated ylidenebutenolide segment 2 and highly functionalized alkenylstannanes. [reaction: see text]

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Year:  2005        PMID： 15704890     DOI： 10.1021/ol0478281

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


  4 in total

1.  Stereoretentive Suzuki-Miyaura coupling of haloallenes enables fully stereocontrolled access to (-)-peridinin.

Authors:  Eric M Woerly; Alan H Cherney; Erin K Davis; Martin D Burke
Journal:  J Am Chem Soc       Date:  2010-05-26       Impact factor: 15.419

2.  Synthesis and cytotoxic activity of some 3-benzyl-5-arylidenefuran-2(5H)-ones.

Authors:  Róbson Ricardo Teixeira; Luiz Cláudio Barbosa; Célia Regina Alvares Maltha; Marcelo Eça Rocha; Daniel Pereira Bezerra; Letícia Veras Costa-Lotuf; Cláudia Pessoa; Manoel Odorico Moraes
Journal:  Molecules       Date:  2007-05-24       Impact factor: 4.411

3.  Peridinin Is an Exceptionally Potent and Membrane-Embedded Inhibitor of Bilayer Lipid Peroxidation.

Authors:  Hannah M S Haley; Adam G Hill; Alexander I Greenwood; Eric M Woerly; Chad M Rienstra; Martin D Burke
Journal:  J Am Chem Soc       Date:  2018-11-02       Impact factor: 15.419

4.  Total synthesis of synechoxanthin through iterative cross-coupling.

Authors:  Seiko Fujii; Stephanie Y Chang; Martin D Burke
Journal:  Angew Chem Int Ed Engl       Date:  2011-06-16       Impact factor: 15.336
  4 in total

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