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.
benzofuran
bond cleavage
cycloisomerization
palladium
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
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