Cross-Coupling Reactions of Nitroarenes.


Journal

Accounts of chemical research
ISSN: 1520-4898
Titre abrégé: Acc Chem Res
Pays: United States
ID NLM: 0157313

Informations de publication

Date de publication:
20 07 2021
Historique:
pubmed: 8 7 2021
medline: 8 7 2021
entrez: 7 7 2021
Statut: ppublish

Résumé

Cross-coupling reactions are powerful synthetic tools to construct diverse chemical bonds often found in, for example, advanced materials and pharmaceuticals. Since their discovery, haloarenes have habitually been used as electrophilic coupling partners both in academic and industrial contexts. However, concerning the efficiency and the often-negative environmental impact of haloarene-based cross-coupling processes, more readily available, inexpensive, and environmentally friendly electrophiles have been explored.Nitroarenes, for example, are obtained from the facile nitration of aromatic compounds and, thus, represent one of the most easy-to-access feedstock electrophiles. Furthermore, their electron-deficient arene core can be functionalized easily and site-selectively through a wide variety of reactions. Yet, despite these advantages and even though the direct transformation of the NO

Identifiants

pubmed: 34232634
doi: 10.1021/acs.accounts.1c00220
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

2928-2935

Auteurs

Myuto Kashihara (M)

Department of Material Chemistry, Graduate School of Engineering, Kyoto University, Kyoto 615-8510, Japan.

Yoshiaki Nakao (Y)

Department of Material Chemistry, Graduate School of Engineering, Kyoto University, Kyoto 615-8510, Japan.

Classifications MeSH