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
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.

Identifiants

pubmed: 32510092
doi: 10.1039/d0ob00956c
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

4533-4546

Auteurs

Alessandro Palmieri (A)

School of Science and Technology, Chemistry Division, University of Camerino, Via S. Agostino n. 1, 62032 Camerino (MC), Italy. marino.petrini@unicam.it.

Marino Petrini (M)

School of Science and Technology, Chemistry Division, University of Camerino, Via S. Agostino n. 1, 62032 Camerino (MC), Italy. marino.petrini@unicam.it.

Classifications MeSH