Literature DB >> 21271686

Facile ring-opening of azabicyclic [3.1.0]- and [4.1.0]aminocyclopropanes to afford 3-piperidinone and 3-azepinone.

Jisun Lee1, Simon Berritt, Christopher K Prier, Madeleine M Joullié.   

Abstract

Azabicyclic [3.1.0] and [4.1.0] Kulinkovich products underwent a facile reduction/fragmentation to afford a variety of 3-piperidinones and 3-azepinones, respectively, in the presence of catalytic palladium on carbon and formic acid in an atmosphere of hydrogen.

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Year:  2011        PMID: 21271686     DOI: 10.1021/ol103105q

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


  2 in total

1.  Intermolecular [3+2] cycloaddition of cyclopropylamines with olefins by visible-light photocatalysis.

Authors:  Soumitra Maity; Mingzhao Zhu; Ryan Spencer Shinabery; Nan Zheng
Journal:  Angew Chem Int Ed Engl       Date:  2011-11-23       Impact factor: 15.336

2.  A Photo Touch on Amines: New Synthetic Adventures of Nitrogen Radical Cations.

Authors:  Soumitira Maity; Nan Zheng
Journal:  Synlett       Date:  2012-07-23       Impact factor: 2.454

  2 in total

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