A facile access to 1-substituted and unsubstituted 3-isoquinolinones


Journal

RSC advances
ISSN: 2046-2069
Titre abrégé: RSC Adv
Pays: England
ID NLM: 101581657

Informations de publication

Date de publication:
21 Feb 2023
Historique:
received: 18 01 2023
accepted: 17 02 2023
entrez: 27 2 2023
pubmed: 28 2 2023
medline: 28 2 2023
Statut: epublish

Résumé

Herein we report new cascade processes for the easy access to 1-substituted and C-unsubstituted 3-isoquinolinones. The Mannich initiated cascade reaction led to the synthesis of novel 1-substituted 3-isoquinolinones under catalyst-free conditions in the presence of nitromethane and dimethylmalonate as nucleophiles without the use of any solvent. The optimization of the synthesis of the starting material in a more environmentally benign manner, allowed the identification of a common intermediate useful for the synthesis of C-unsubstituted 3-isoquinolinones as well. The synthetic utility of 1-substituted 3-isoquinolinones was also demonstrated.

Identifiants

pubmed: 36845590
doi: 10.1039/d3ra00378g
pii: d3ra00378g
pmc: PMC9951188
doi:

Types de publication

Journal Article

Langues

eng

Pagination

6557-6563

Informations de copyright

This journal is © The Royal Society of Chemistry.

Déclaration de conflit d'intérêts

There are no conflicts to declare.

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Auteurs

Lorenzo Serusi (L)

Dipartimento di Chimica e Biologia "A. Zambelli", Università degli Studi di Salerno Via Giovanni Paolo II, 84084 Fisciano Italy adimola@unisa.it amassa@unisa.it.

Antonia Di Mola (A)

Dipartimento di Chimica e Biologia "A. Zambelli", Università degli Studi di Salerno Via Giovanni Paolo II, 84084 Fisciano Italy adimola@unisa.it amassa@unisa.it.

Antonio Massa (A)

Dipartimento di Chimica e Biologia "A. Zambelli", Università degli Studi di Salerno Via Giovanni Paolo II, 84084 Fisciano Italy adimola@unisa.it amassa@unisa.it.

Classifications MeSH