Literature DB >> 17221964

Oxidative and reductive carbodiazenylation of nonactivated olefins.

Markus R Heinrich1, Olga Blank, Alexander Wetzel.   

Abstract

Procedures for the carbodiazenylation of nonactivated olefins with a wide range of aryldiazonium salts have been developed. The azo compounds obtained can serve as valuable precursors for beta-arylamines (carboamination products), beta-amino acids, ketones, and various heterocyclic structures.

Entities:  

Year:  2007        PMID: 17221964     DOI: 10.1021/jo061919p

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  1 in total

1.  (E)-1-[(2,4,6-Tri-bromo-phen-yl)diazen-yl]naphthalen-2-ol.

Authors:  Souheyla Chetioui; Issam Boudraa; Sofiane Bouacida; Abdelkader Bouchoul; Salah Eddine Bouaoud
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2013-07-13
  1 in total

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