Green Synthesis of Privileged Benzimidazole Scaffolds Using Active Deep Eutectic Solvent.
aromatic amines
benzimidazoles
deep eutectic solvents
green chemistry
heterocyclic moiety
Journal
Molecules (Basel, Switzerland)
ISSN: 1420-3049
Titre abrégé: Molecules
Pays: Switzerland
ID NLM: 100964009
Informations de publication
Date de publication:
08 Aug 2019
08 Aug 2019
Historique:
received:
09
07
2019
revised:
02
08
2019
accepted:
07
08
2019
entrez:
11
8
2019
pubmed:
11
8
2019
medline:
10
1
2020
Statut:
epublish
Résumé
The exploitation and use of alternative synthetic methods, in the face of classical procedures that do not conform to the ethics of green chemistry, represent an ever-present problem in the pharmaceutical industry. The procedures for the synthesis of benzimidazoles have become a focus in synthetic organic chemistry, as they are building blocks of strong interest for the development of compounds with pharmacological activity. Various benzimidazole derivatives exhibit important activities such as antimicrobial, antiviral, anti-inflammatory, and analgesic activities, and some of the already synthesized compounds have found very strong applications in medicine praxis. Here we report a selective and sustainable method for the synthesis of 1,2-disubstituted or 2-substituted benzimidazoles, starting from
Identifiants
pubmed: 31398916
pii: molecules24162885
doi: 10.3390/molecules24162885
pmc: PMC6719900
pii:
doi:
Substances chimiques
Benzimidazoles
0
Solvents
0
benzimidazole
E24GX49LD8
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Références
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