Tricyclic 2-benzazepines obtained


Journal

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

Informations de publication

Date de publication:
16 06 2021
Historique:
pubmed: 25 5 2021
medline: 25 5 2021
entrez: 24 5 2021
Statut: ppublish

Résumé

Attempted use of (E)-3-arylidene-4-diazopyrrolidine-2,5-diones in the Rh(ii)-catalyzed condensation with nitriles to form 1,3-oxazoles led to an unexpected outcome. The nitrilium ylide species thought to form on Rh(ii)-catalyzed decomposition of diazo compounds underwent a cyclization onto the nearby arylidene moiety followed by 1,5-hydride shift. This led to the formation of a 2-benzazepine core which has special significance for drug discovery and can be considered a privileged scaffold.

Identifiants

pubmed: 34027962
doi: 10.1039/d1ob00773d
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

5068-5071

Auteurs

Anna Inyutina (A)

Institute of Chemistry, Saint Petersburg State University, Saint Petersburg 199034, Russian Federation. m.krasavin@spbu.ru d.dariin@spbu.ru.

Dmitry Dar'in (D)

Institute of Chemistry, Saint Petersburg State University, Saint Petersburg 199034, Russian Federation. m.krasavin@spbu.ru d.dariin@spbu.ru.

Grigory Kantin (G)

Institute of Chemistry, Saint Petersburg State University, Saint Petersburg 199034, Russian Federation. m.krasavin@spbu.ru d.dariin@spbu.ru.

Mikhail Krasavin (M)

Institute of Chemistry, Saint Petersburg State University, Saint Petersburg 199034, Russian Federation. m.krasavin@spbu.ru d.dariin@spbu.ru.

Classifications MeSH