On the mechanism of carboxylate elimination from carbohydrate monoester-derived radicals.


Journal

Organic & biomolecular chemistry
ISSN: 1477-0539
Titre abrégé: Org Biomol Chem
Pays: England
ID NLM: 101154995

Informations de publication

Date de publication:
10 Apr 2024
Historique:
medline: 10 4 2024
pubmed: 10 4 2024
entrez: 10 4 2024
Statut: aheadofprint

Résumé

A computational study of the mechanism of hydrogen atom transfer-induced carboxylate elimination from monoacylated 1,2-diol groups in pyranosides is presented. A comprehensive analysis of the 1,2-migration, elimination and fragmentation pathways reveals that concerted elimination

Identifiants

pubmed: 38597089
doi: 10.1039/d4ob00241e
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Julia A Turner (JA)

Department of Chemistry, University of Toronto, 80 St. George St, Toronto, ON M5S 3H6, Canada. mtaylor@chem.utoronto.ca.

Hendrik Zipse (H)

Department Chemie, Ludwig-Maximilians-Universität München, Butenandtstrasse 5-13, Haus F, 81377 München, Germany. zipse@cup.uni-muenchen.de.

Mark S Taylor (MS)

Department of Chemistry, University of Toronto, 80 St. George St, Toronto, ON M5S 3H6, Canada. mtaylor@chem.utoronto.ca.

Classifications MeSH