Literature DB >> 14507227

First total synthesis and stereochemical definition of isodomoic acid G.

Yike Ni1, Kande K D Amarasinghe, Bashar Ksebati, John Montgomery.   

Abstract

[structure: see text] The first total synthesis and stereochemical definition of isodomoic acid G has been achieved. The key nickel-catalyzed coupling of an alkynyl enone with an alkenylzirconium allows formation of the pyrrolidine ring and most of the stereochemical features in a single step. This report provides the first total synthesis application of this new reaction and illustrates its utility in the stereoselective preparation of highly substituted 1,3-dienes.

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Year:  2003        PMID: 14507227     DOI: 10.1021/ol0355783

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


  5 in total

1.  Metallacycle-Mediated Cross-Coupling in Natural Product Synthesis.

Authors:  Natasha F O'Rourke; Matthew J Kier; Glenn C Micalizio
Journal:  Tetrahedron       Date:  2016-09-07       Impact factor: 2.457

2.  Stereocontrolled total syntheses of isodomoic acids G and H via a unified strategy.

Authors:  Scott E Denmark; Jack Hung-Chang Liu; Joseck M Muhuhi
Journal:  J Org Chem       Date:  2010-12-01       Impact factor: 4.354

3.  Nickel-catalyzed cyclizations of enoates and chiral allenes: an approach to domoic acid.

Authors:  Ahmad S ElDouhaibi; Refaie M Kassab; Minsoo Song; John Montgomery
Journal:  Chemistry       Date:  2011-04-27       Impact factor: 5.236

4.  Total syntheses of isodomoic acids G and H: an exercise in tetrasubstituted alkene synthesis.

Authors:  Yike Ni; Refaie M Kassab; Maxim V Chevliakov; John Montgomery
Journal:  J Am Chem Soc       Date:  2009-12-09       Impact factor: 15.419

5.  Total syntheses of isodomoic acids G and H.

Authors:  Scott E Denmark; Jack Hung-Chang Liu; Joseck M Muhuhi
Journal:  J Am Chem Soc       Date:  2009-10-14       Impact factor: 15.419

  5 in total

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