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Transformations of Isonitriles with Bromoalkanes Using Photoredox Gold Catalysis.
Rohe, Samantha; McCallum, Terry; Morris, Avery O; Barriault, Louis.
Afiliação
  • Rohe S; Centre for Catalysis, Research and Innovation Department of Chemistry and Biomolecular Sciences , University of Ottawa , 10 Marie Curie , Ottawa , Ontario K1N 6N5 , Canada.
  • McCallum T; Centre for Catalysis, Research and Innovation Department of Chemistry and Biomolecular Sciences , University of Ottawa , 10 Marie Curie , Ottawa , Ontario K1N 6N5 , Canada.
  • Morris AO; Centre for Catalysis, Research and Innovation Department of Chemistry and Biomolecular Sciences , University of Ottawa , 10 Marie Curie , Ottawa , Ontario K1N 6N5 , Canada.
  • Barriault L; Centre for Catalysis, Research and Innovation Department of Chemistry and Biomolecular Sciences , University of Ottawa , 10 Marie Curie , Ottawa , Ontario K1N 6N5 , Canada.
J Org Chem ; 83(17): 10015-10024, 2018 Sep 07.
Article em En | MEDLINE | ID: mdl-29979602
ABSTRACT
Isonitriles have excellent electronic compatibility to react with free radicals. Recently, photoredox catalysis has emerged as a powerful tool for the construction of C-C bonds with few protocols for alkylative heterocycle synthesis through isonitrile addition. Herein, we describe the photocatalytic generation of alkyl radicals from unactivated bromoalkanes as part of an efficient cross-coupling strategy for the diversification of isonitriles using a dimeric gold(I) photoredox catalyst, [Au2(dppm)2]Cl2.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Org Chem Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Org Chem Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Canadá