Literature DB >> 22388440

An unexpected disproportional reaction of 2H-azirines giving (1E,3Z)-2-aza-1,3-dienes and aromatic nitriles in the presence of nickel catalysts.

Kazuhiro Okamoto1, Ayano Mashida, Masahito Watanabe, Kouichi Ohe.   

Abstract

An unprecedented nickel-catalysed disproportional reaction of 2,3-diaryl-2H-azirines forming azabutadienes and aromatic nitriles was discovered. This reaction involves the cleavage of two bonds of the 2H-azirine framework, which provides a novel type of transformation of 2H-azirines. This journal is © The Royal Society of Chemistry 2012

Entities:  

Year:  2012        PMID: 22388440     DOI: 10.1039/c2cc30745f

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

1.  Diverse Reactivity of Diazatitanacyclohexenes: Coupling Reactions of 2H-Azirines Mediated by Titanium(II).

Authors:  Addison N Desnoyer; Xin Yi See; Ian A Tonks
Journal:  Organometallics       Date:  2018-09-10       Impact factor: 3.876

2.  Investigation on the reactivity of α-azidochalcones with carboxylic acids: Formation of α-amido-1,3-diketones and highly substituted 2-(trifluoromethyl)oxazoles.

Authors:  Kandasamy Rajaguru; Arumugam Mariappan; Rajendran Suresh; Periasamy Manivannan; Shanmugam Muthusubramanian
Journal:  Beilstein J Org Chem       Date:  2015-10-29       Impact factor: 2.883

  2 in total

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