Deprotonative Coupling of Pyridines with Aldehydes Catalyzed by an HMDS-Amide Base Generated in Situ.


Journal

Chemical & pharmaceutical bulletin
ISSN: 1347-5223
Titre abrégé: Chem Pharm Bull (Tokyo)
Pays: Japan
ID NLM: 0377775

Informations de publication

Date de publication:
2019
Historique:
entrez: 6 11 2019
pubmed: 7 11 2019
medline: 14 1 2020
Statut: ppublish

Résumé

Herein, the deprotonative functionalization of pyridine derivatives with aldehydes under ambient conditions has been demonstrated using an amide base generated in situ from a catalytic amount of CsF and a stoichiometric amount of tris(trimethylsilyl)amine (N(TMS)

Identifiants

pubmed: 31685747
doi: 10.1248/cpb.c19-00589
doi:

Substances chimiques

Aldehydes 0
Amides 0
Organosilicon Compounds 0
Protons 0
Pyridines 0
hexamethylsilazane H36C68P1BH

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1179-1182

Auteurs

Masanori Shigeno (M)

Department of Biophysical Chemistry, Graduate School of Pharmaceutical Sciences, Tohoku University.

Kunihito Nakaji (K)

Department of Biophysical Chemistry, Graduate School of Pharmaceutical Sciences, Tohoku University.

Akihisa Kajima (A)

Department of Biophysical Chemistry, Graduate School of Pharmaceutical Sciences, Tohoku University.

Kanako Nozawa-Kumada (K)

Department of Biophysical Chemistry, Graduate School of Pharmaceutical Sciences, Tohoku University.

Yoshinori Kondo (Y)

Department of Biophysical Chemistry, Graduate School of Pharmaceutical Sciences, Tohoku University.

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Classifications MeSH