Literature DB >> 20443571

Expeditious synthesis of highly substituted indolizinones via a palladium-catalyzed domino sequence.

Ikyon Kim1, Kyungsun Kim.   

Abstract

A direct one-pot approach to polysubstituted indolizinones from tertiary propargylic alcohols using a palladium-catalyzed domino process involving aminopalladation, reductive elimination, and 1,2-shift is described.

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Year:  2010        PMID： 20443571     DOI： 10.1021/ol1006778

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


  2 in total

1.  Two-component approach toward a fully substituted N-fused pyrrole ring.

Authors:  Dmitri Chernyak; Cathy Skontos; Vladimir Gevorgyan
Journal:  Org Lett       Date:  2010-07-16       Impact factor: 6.005

2.  Asymmetric synthesis of 1H-pyrrol-3(2H)-ones from 2,3-diketoesters by combination of aldol condensation with benzilic acid rearrangement.

Authors:  Qiang Sha; Hadi Arman; Michael P Doyle
Journal:  Chem Commun (Camb)       Date:  2016-01-04       Impact factor: 6.222
  2 in total

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