Literature DB >> 18494527

Synthesis of highly labile SG1-based alkoxyamines under photochemical conditions.

Yohann Guillaneuf1, Jean-Luc Couturier, Didier Gigmes, Sylvain R A Marque, Paul Tordo, Denis Bertin.   

Abstract

Highly labile SG1-based alkoxyamines were synthesized using the photodecomposition of both azo compounds and dithiocarbamates. The former method was a straightforward procedure to obtain the alkoxyamines, but a high [azo]/[nitroxide] ratio is needed. The latter method required only a stoichiometric amount of dithiocarbamate and allowed the recovery of the disulfide after irradiation. This enabled combination of the two methods in a process where only 0.75 equiv of azo compound is needed and where sulfurous compounds acted only as intermediates.

Entities:  

Year:  2008        PMID: 18494527     DOI: 10.1021/jo800422a

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


  1 in total

1.  One-pot three-component route for the synthesis of S-trifluoromethyl dithiocarbamates using Togni's reagent.

Authors:  Azim Ziyaei Halimehjani; Martin Dračínský; Petr Beier
Journal:  Beilstein J Org Chem       Date:  2017-11-24       Impact factor: 2.883

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.