Double asymmetric synthesis: faster reactions are more selective and a model to estimate relative rate.


Journal

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

Informations de publication

Date de publication:
13 Sep 2023
Historique:
medline: 21 8 2023
pubmed: 21 8 2023
entrez: 21 8 2023
Statut: epublish

Résumé

The catalysed reaction of an enantiopure substrate with formation of a new chirality element may result in higher diastereoselectivity with one enantiomer of a catalyst (matched pair) than with the other (mismatched pair). The hypothesis that the matched reaction is faster was investigated using literature examples of kinetic resolution procedures that result in the formation of a new stereogenic centre. With one exception from fifteen examples, the selectivity factor (

Identifiants

pubmed: 37599596
doi: 10.1039/d3ob01048a
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

7115-7128

Auteurs

Christopher J Richards (CJ)

School of Chemistry, University of East Anglia, Norwich, NR4 7TJ, UK. Chris.Richards@uea.ac.uk.

O Stephen Ojo (O)

School of Chemistry, University of East Anglia, Norwich, NR4 7TJ, UK. Chris.Richards@uea.ac.uk.

Classifications MeSH