Literature DB >> 28949540

Organocatalytic β-Azidation of Enones Initiated by an Electron-Donor-Acceptor Complex.

Rajendra P Shirke1, S S V Ramasastry1.   

Abstract

An operationally straightforward organocatalytic β-azidation of α,β-unsaturated ketones is described. Reaction of the Zhdankin azidoiodane with enones in the presence of a catalytic amount of an amine provides β-azido ketones via the formation of an electron-donor-acceptor complex. The application of this protocol is demonstrated through one-step elaborations leading to the synthesis of unprecedented classes of 1,2,3-triazoles.

Entities:  

Year:  2017        PMID: 28949540     DOI: 10.1021/acs.orglett.7b02861

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


  3 in total

1.  Regiocontrolled Wacker Oxidation of Cinnamyl Azides.

Authors:  Angela S Carlson; Cristian Calcanas; Ryan M Brunner; Joseph J Topczewski
Journal:  Org Lett       Date:  2018-03-02       Impact factor: 6.005

2.  Alkene 1,2-Difunctionalization by Radical Alkenyl Migration.

Authors:  Xinjun Tang; Armido Studer
Journal:  Angew Chem Int Ed Engl       Date:  2017-12-14       Impact factor: 15.336

3.  Synthetic Methods Driven by the Photoactivity of Electron Donor-Acceptor Complexes.

Authors:  Giacomo E M Crisenza; Daniele Mazzarella; Paolo Melchiorre
Journal:  J Am Chem Soc       Date:  2020-03-12       Impact factor: 15.419

  3 in total

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