Literature DB >> 33634699

Coupling Photocatalysis and Substitution Chemistry to Expand and Normalize Redox-Active Halides.

Manjula D Rathnayake1, Jimmie D Weaver1.   

Abstract

Photocatalysis can generate radicals in a controlled fashion and has become an important synthetic strategy. However, limitations due to the reducibility of alkyl halides prevent their broader implementation. Herein we explore the use of nucleophiles that can substitute the halide and serve as an electron capture motif that normalize the variable redox potentials across substrates. When used with photocatalysis, bench-stable, commercially available collidinium salts prove to be excellent radical precursors with a broad scope.

Entities:  

Year:  2021        PMID: 33634699     DOI: 10.1021/acs.orglett.1c00173

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


  3 in total

1.  Direct Deamination of Primary Amines via Isodiazene Intermediates.

Authors:  Kathleen J Berger; Julia L Driscoll; Mingbin Yuan; Balu D Dherange; Osvaldo Gutierrez; Mark D Levin
Journal:  J Am Chem Soc       Date:  2021-10-12       Impact factor: 15.419

2.  Site-Selective Synthesis of N-Benzyl 2,4,6-Collidinium Salts by Electrooxidative C-H Functionalization.

Authors:  Bill J Motsch; Sarah E Wengryniuk
Journal:  Org Lett       Date:  2022-08-08       Impact factor: 6.072

3.  Heterocyclic group transfer reactions with I(iii) N-HVI reagents: access to N-alkyl(heteroaryl)onium salts via olefin aminolactonization.

Authors:  Anthony F Tierno; Jennifer C Walters; Andres Vazquez-Lopez; Xiao Xiao; Sarah E Wengryniuk
Journal:  Chem Sci       Date:  2021-04-12       Impact factor: 9.969

  3 in total

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