NaH-mediated direct C-H arylation in the presence of 1,10-phenanthroline.


Journal

Chemical communications (Cambridge, England)
ISSN: 1364-548X
Titre abrégé: Chem Commun (Camb)
Pays: England
ID NLM: 9610838

Informations de publication

Date de publication:
14 Jul 2020
Historique:
pubmed: 24 6 2020
medline: 24 6 2020
entrez: 24 6 2020
Statut: ppublish

Résumé

Transition-metal-free coupling of haloarenes with unactivated arenes has been developed in the presence of NaH and 1,10-phenanthroline. Various haloarenes bearing methyl, methoxy, halogen (fluoride, chloride, and bromide), cyano, trifluoromethyl, ester, and amide groups can be cross-coupled with unactivated arenes, or heteroarenes in this reaction.

Identifiants

pubmed: 32573564
doi: 10.1039/d0cc00730g
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

7773-7776

Auteurs

Kanako Nozawa-Kumada (K)

Graduate School of Pharmaceutical Sciences, Tohoku University, 6-3 Aoba, Aramaki, Aoba-ku, Sendai 980-8578, Japan. kumada@m.tohoku.ac.jp ykondo@m.tohoku.ac.jp.

Yuki Iwakawa (Y)

Graduate School of Pharmaceutical Sciences, Tohoku University, 6-3 Aoba, Aramaki, Aoba-ku, Sendai 980-8578, Japan. kumada@m.tohoku.ac.jp ykondo@m.tohoku.ac.jp.

So Onuma (S)

Graduate School of Pharmaceutical Sciences, Tohoku University, 6-3 Aoba, Aramaki, Aoba-ku, Sendai 980-8578, Japan. kumada@m.tohoku.ac.jp ykondo@m.tohoku.ac.jp.

Masanori Shigeno (M)

Graduate School of Pharmaceutical Sciences, Tohoku University, 6-3 Aoba, Aramaki, Aoba-ku, Sendai 980-8578, Japan. kumada@m.tohoku.ac.jp ykondo@m.tohoku.ac.jp.

Yoshinori Kondo (Y)

Graduate School of Pharmaceutical Sciences, Tohoku University, 6-3 Aoba, Aramaki, Aoba-ku, Sendai 980-8578, Japan. kumada@m.tohoku.ac.jp ykondo@m.tohoku.ac.jp.

Classifications MeSH