Palladium-Catalyzed Intramolecular Migratory Cycloisomerization of 3-Phenoxy Acrylic Acid Ester via C-O Bond Cleavage and C-O/C-C Bonds Formation for 2,3-Disubstituted Benzofurans Synthesis.


Journal

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

Informations de publication

Date de publication:
2023
Historique:
entrez: 1 2 2023
pubmed: 2 2 2023
medline: 4 2 2023
Statut: ppublish

Résumé

Migratory cycloisomerization using transition metal catalyst is useful for synthesizing substituted heterocyclic compounds. We achieved palladium-catalyzed migratory cycloisomerization of 3-o-alkynylphenoxy acrylic acid ester derivatives to give 2,3-disubstituted benzofurans. Although there are several reports of benzofuran synthesis with palladium-catalyzed migratory cycloisomerization, migratory groups are limited to allyl and propargyl groups. This report is the first example of benzofuran synthesis with palladium-catalyzed cycloisomerization of C(sp

Identifiants

pubmed: 36724985
doi: 10.1248/cpb.c22-00555
doi:

Substances chimiques

Palladium 5TWQ1V240M
acrylic acid J94PBK7X8S
Benzofurans 0
Heterocyclic Compounds 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

93-100

Auteurs

Yuichi Kuboki (Y)

Graduate School of Pharmaceutical Sciences, Osaka University.

Shohei Ohno (S)

Graduate School of Pharmaceutical Sciences, Osaka University.

Makoto Sako (M)

Graduate School of Pharmaceutical Sciences, Osaka University.

Kenichi Murai (K)

Graduate School of Pharmaceutical Sciences, Osaka University.

Mitsuhiro Arisawa (M)

Graduate School of Pharmaceutical Sciences, Osaka University.

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Classifications MeSH