Urethanes synthesis from oxamic acids under electrochemical conditions.


Journal

Chemical communications (Cambridge, England)
ISSN: 1364-548X
Titre abrégé: Chem Commun (Camb)
Pays: England
ID NLM: 9610838

Informations de publication

Date de publication:
13 Oct 2020
Historique:
pubmed: 15 9 2020
medline: 15 9 2020
entrez: 14 9 2020
Statut: ppublish

Résumé

Urethane synthesis via oxidative decarboxylation of oxamic acids under mild electrochemical conditions is reported. This simple phosgene-free route to urethanes involves an in situ generation of isocyanates by anodic oxidation of oxamic acids in an alcoholic medium. The reaction is applicable to a wide range of oxamic acids, including chiral ones, and alcohols furnishing the desired urethanes in a one-pot process without the use of a chemical oxidant.

Identifiants

pubmed: 32926019
doi: 10.1039/d0cc05069e
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

12226-12229

Auteurs

Ikechukwu Martin Ogbu (IM)

University of Bordeaux, Institute of Molecular Sciences (ISM), UMR-CNRS 5255, 351, Cours de la Libération, 33405 Talence Cedex, France. yannick.landais@u-bordeaux.fr.

Jonathan Lusseau (J)

University of Bordeaux, Institute of Molecular Sciences (ISM), UMR-CNRS 5255, 351, Cours de la Libération, 33405 Talence Cedex, France. yannick.landais@u-bordeaux.fr.

Gülbin Kurtay (G)

University of Bordeaux, Institute of Molecular Sciences (ISM), UMR-CNRS 5255, 351, Cours de la Libération, 33405 Talence Cedex, France. yannick.landais@u-bordeaux.fr.

Frédéric Robert (F)

University of Bordeaux, Institute of Molecular Sciences (ISM), UMR-CNRS 5255, 351, Cours de la Libération, 33405 Talence Cedex, France. yannick.landais@u-bordeaux.fr.

Yannick Landais (Y)

University of Bordeaux, Institute of Molecular Sciences (ISM), UMR-CNRS 5255, 351, Cours de la Libération, 33405 Talence Cedex, France. yannick.landais@u-bordeaux.fr.

Classifications MeSH