Synthesis and practical applications of 2-(2-nitroalkyl)pyrroles.
Journal
Organic & biomolecular chemistry
ISSN: 1477-0539
Titre abrégé: Org Biomol Chem
Pays: England
ID NLM: 101154995
Informations de publication
Date de publication:
24 06 2020
24 06 2020
Historique:
pubmed:
9
6
2020
medline:
9
6
2020
entrez:
9
6
2020
Statut:
ppublish
Résumé
Functionalization of pyrroles introducing a 2-nitroalkyl moiety allows the formation of nitro-containing compounds to be used as pivotal intermediates for the synthesis of bioactive compounds. The reaction of pyrroles with nitroalkenes under the Friedel-Crafts conditions allows a direct entry to 2-(2-nitroalkyl)pyrroles. This approach can also be used for the preparation of enantioenriched derivatives exploiting asymmetric catalysis. In a complementary fashion, the Henry reaction between 2-formylpyrroles and nitroalkanes generates the corresponding nitroaldol products which upon dehydration and reduction of the intermediate 2-pyrrolylnitroethene efficiently afford 2-(2-nitroalkyl)pyrroles. This review article summarizes the most relevant procedures for the preparation of 2-(2-nitroalkyl)pyrroles during the last two decades as well as their significant practical applications.
Types de publication
Journal Article
Review
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM