Literature DB >> 24839111

Access to oxoquinoline heterocycles by N-heterocyclic carbene catalyzed ester activation for selective reaction with an enone.

Zhenqian Fu1, Ke Jiang, Tingshun Zhu, Jaume Torres, Yonggui Robin Chi.   

Abstract

Organocatalytic ester activation is developed for a highly selective cascade reaction between saturated esters and amino enones. The reaction involves activation of the β-carbon atom of the ester as a key step. This method allows a single-step access to multicyclic oxoquinoline-type heterocycles with high enantiomeric ratios.
© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  CH activation; N-heterocyclic carbene; cyclization; heterocycles; organocatalysis

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Year:  2014        PMID: 24839111     DOI: 10.1002/anie.201402620

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  2 in total

Review 1.  N-Heterocyclic-Carbene-Catalyzed Domino Reactions via Two or More Activation Modes.

Authors:  Xiang-Yu Chen; Sun Li; Fabrizio Vetica; Mukesh Kumar; Dieter Enders
Journal:  iScience       Date:  2018-04-05

2.  Synergetic iridium and amine catalysis enables asymmetric [4+2] cycloadditions of vinyl aminoalcohols with carbonyls.

Authors:  Mao-Mao Zhang; Ya-Ni Wang; Bao-Cheng Wang; Xiao-Wang Chen; Liang-Qiu Lu; Wen-Jing Xiao
Journal:  Nat Commun       Date:  2019-06-20       Impact factor: 14.919

  2 in total

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