Multi-component synthesis of dihydro-1,3-azaborinine derived oxindole isosteres.


Journal

Chemical communications (Cambridge, England)
ISSN: 1364-548X
Titre abrégé: Chem Commun (Camb)
Pays: England
ID NLM: 9610838

Informations de publication

Date de publication:
03 Aug 2021
Historique:
pubmed: 15 7 2021
medline: 15 7 2021
entrez: 14 7 2021
Statut: ppublish

Résumé

We report on the synthesis of the first examples of 1,3-azaborinine derived oxindole systems, the BN-isosteres of the important compound class of the oxindoles. Hydroboration of terminal aryl acetylenes with FmesBH2, followed by treatment with 2 equiv. of a glycine ester derived isonitrile gave a small series of 1,3-azaborinine derived oxindoles. The new BN-oxindoles show interesting photophysical behavior.

Identifiants

pubmed: 34259251
doi: 10.1039/d1cc02557k
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

7689-7692

Auteurs

Jun Li (J)

Organisch-Chemisches Institut, Westfälische Wilhelms-Universität Münster, Corrensstraβe 40, 48149, Münster, Germany. erker@uni-muenster.de.

Constantin G Daniliuc (CG)

Organisch-Chemisches Institut, Westfälische Wilhelms-Universität Münster, Corrensstraβe 40, 48149, Münster, Germany. erker@uni-muenster.de.

Jonas Matern (J)

Organisch-Chemisches Institut, Westfälische Wilhelms-Universität Münster, Corrensstraβe 40, 48149, Münster, Germany. erker@uni-muenster.de.

Gustavo Fernández (G)

Organisch-Chemisches Institut, Westfälische Wilhelms-Universität Münster, Corrensstraβe 40, 48149, Münster, Germany. erker@uni-muenster.de.

Gerald Kehr (G)

Organisch-Chemisches Institut, Westfälische Wilhelms-Universität Münster, Corrensstraβe 40, 48149, Münster, Germany. erker@uni-muenster.de.

Gerhard Erker (G)

Organisch-Chemisches Institut, Westfälische Wilhelms-Universität Münster, Corrensstraβe 40, 48149, Münster, Germany. erker@uni-muenster.de.

Classifications MeSH