Literature DB >> 20863078

Efficient catalytic, oxidative lactonization for the synthesis of benzodioxepinones using thiazolium-derived carbene catalysts.

Christopher A Rose1, Kirsten Zeitler.   

Abstract

An efficient, oxidative carbene-catalyzed lactonization reaction has been developed. Using thiazolium precatalysts, a variety of benzodioxepinone products are accessible in good to excellent yields under mild and operationally simple conditions. The reaction does not require high dilution conditions and proceeds via mild and selective oxidation with azobenzene, which can easily be recovered and reused applying inexpensive FeCl(3) as a formal terminal oxidant.

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Year:  2010        PMID: 20863078     DOI: 10.1021/ol101854r

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


  3 in total

1.  On the role of CO2 in NHC-catalyzed oxidation of aldehydes.

Authors:  Pei-Chen Chiang; Jeffrey W Bode
Journal:  Org Lett       Date:  2011-04-12       Impact factor: 6.005

2.  New oxacycles on the block: benzodioxepinones via a Passerini reaction.

Authors:  Michael Fragkiadakis; Marios Zingiridis; Edward Loukopoulos; Constantinos G Neochoritis
Journal:  Mol Divers       Date:  2022-07-28       Impact factor: 3.364

3.  NHC-catalysed highly selective aerobic oxidation of nonactivated aldehydes.

Authors:  Lennart Möhlmann; Stefan Ludwig; Siegfried Blechert
Journal:  Beilstein J Org Chem       Date:  2013-03-22       Impact factor: 2.883

  3 in total

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