Literature DB >> 20356101

Diversity-oriented construction of highly substituted indolizinones.

Kyungsun Kim1, Ikyon Kim.   

Abstract

Rapid generation of a small library of highly functionalized indolizonones was realized by exploiting three palladium-catalyzed cross-coupling reactions of 2-iodoindolizinones which in turn were readily accessed via sequential iodine-mediated cyclization/1,2-shift reactions of propargylic alcohols.

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Year:  2010        PMID: 20356101     DOI: 10.1021/cc100015k

Source DB:  PubMed          Journal:  J Comb Chem        ISSN: 1520-4766


  2 in total

1.  Indolizinones as synthetic scaffolds: fundamental reactivity and the relay of stereochemical information.

Authors:  Alison R Hardin Narayan; Richmond Sarpong
Journal:  Org Biomol Chem       Date:  2011-11-09       Impact factor: 3.876

2.  Symmetry-based approach to oligostilbenoids: Rapid entry to viniferifuran, shoreaphenol, malibatol A, and diptoindonesin G.

Authors:  Youngeun Jung; Dileep Kumar Singh; Ikyon Kim
Journal:  Beilstein J Org Chem       Date:  2016-12-12       Impact factor: 2.883

  2 in total

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