Metal-free decarboxylative allylation of oxime esters under light irradiation.

Photocatlysis - Allylation - oxime esters - metal-free

Journal

Chemistry (Weinheim an der Bergstrasse, Germany)
ISSN: 1521-3765
Titre abrégé: Chemistry
Pays: Germany
ID NLM: 9513783

Informations de publication

Date de publication:
24 May 2024
Historique:
revised: 07 05 2024
received: 17 04 2024
accepted: 24 05 2024
medline: 24 5 2024
pubmed: 24 5 2024
entrez: 24 5 2024
Statut: aheadofprint

Résumé

Allylation reactions, often used as a key step for constructing complex molecules and drug candidates, typically rely on transition-metal (TM) catalysts. Even though TM-free radical allylations have been developed using allyl-stannanes, -sulfides, -silanes or -sulfones, much less procedures have been reported using simple and commercially available allyl halides, that are used for the preparation of the before-mentioned allyl derivatives. Here, we present a straightforward photocatalytic protocol for the decarboxylative allylation of oxime esters using allyl bromide derivatives under metal-free and mild conditions. This methodology yields a diverse variety of functionalized molecules including several pharmaceutically relevant molecules.

Identifiants

pubmed: 38785147
doi: 10.1002/chem.202401494
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e202401494

Informations de copyright

© 2024 Wiley‐VCH GmbH.

Auteurs

Lilian Geniller (L)

Charles Gerhardt of Montpellier Institute, D1, FRANCE.

Hiba Ben Kraim (H)

Charles Gerhardt of Montpellier Institute, D1, FRANCE.

Eric Clot (E)

Charles Gerhardt of Montpellier Institute, D5, FRANCE.

Marc Taillefer (M)

Charles Gerhardt of Montpellier Institute, D1, FRANCE.

Florian Jaroschik (F)

Charles Gerhardt of Montpellier Institute, D1, FRANCE.

Alexis Prieto (A)

ICGM: Institut Charles Gerhardt de Montpellier, D1, 1919 Route de Mende, 34000, MONTPELLIER CEDEX 5, FRANCE.

Classifications MeSH