Literature DB >> 34027962

Tricyclic 2-benzazepines obtained via an unexpected cyclization involving nitrilium ylides.

Anna Inyutina1, Dmitry Dar'in1, Grigory Kantin1, Mikhail Krasavin1.   

Abstract

Attempted use of (E)-3-arylidene-4-diazopyrrolidine-2,5-diones in the Rh(ii)-catalyzed condensation with nitriles to form 1,3-oxazoles led to an unexpected outcome. The nitrilium ylide species thought to form on Rh(ii)-catalyzed decomposition of diazo compounds underwent a cyclization onto the nearby arylidene moiety followed by 1,5-hydride shift. This led to the formation of a 2-benzazepine core which has special significance for drug discovery and can be considered a privileged scaffold.

Entities:  

Year:  2021        PMID: 34027962     DOI: 10.1039/d1ob00773d

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  1 in total

1.  Unusual highly diastereoselective Rh(II)-catalyzed dimerization of 3-diazo-2-arylidenesuccinimides provides access to a new dibenzazulene scaffold.

Authors:  Anastasia Vepreva; Alexander S Bunev; Andrey Yu Kudinov; Grigory Kantin; Mikhail Krasavin; Dmitry Dar'in
Journal:  Beilstein J Org Chem       Date:  2022-05-11       Impact factor: 2.544

  1 in total

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