One-pot, three-component Fischer indolisation-


Journal

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

Informations de publication

Date de publication:
28 01 2021
Historique:
pubmed: 29 12 2020
medline: 29 12 2020
entrez: 28 12 2020
Statut: ppublish

Résumé

A one-pot, three-component protocol for the synthesis of 1,2,3-trisubstituted indoles has been developed, based upon a Fischer indolisation-indole N-alkylation sequence. This procedure is very rapid (total reaction time under 30 minutes), operationally straightforward, generally high yielding and draws upon readily available building blocks (aryl hydrazines, ketones, alkyl halides) to generate densely substituted indole products. We have demonstrated the utility of this process in the synthesis of 23 indoles, benzoindoles and tetrahydrocarbazoles bearing varied and useful functionality.

Identifiants

pubmed: 33367375
doi: 10.1039/d0ob02185g
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

627-634

Auteurs

Christopher A Hughes-Whiffing (CA)

Biosciences, University of Exeter, Stocker Road, Exeter EX4 4QD, UK. A.Perry@Exeter.ac.uk.

Alexis Perry (A)

Biosciences, University of Exeter, Stocker Road, Exeter EX4 4QD, UK. A.Perry@Exeter.ac.uk.

Classifications MeSH