Nickel-Catalyzed Domino Heck-Type Reactions Using Methyl Esters as Cross-Coupling Electrophiles.
cross-coupling
cyclizations
esters
homogeneous catalysis
nickel
Journal
Angewandte Chemie (International ed. in English)
ISSN: 1521-3773
Titre abrégé: Angew Chem Int Ed Engl
Pays: Germany
ID NLM: 0370543
Informations de publication
Date de publication:
09 Dec 2019
09 Dec 2019
Historique:
received:
05
09
2019
pubmed:
2
10
2019
medline:
2
10
2019
entrez:
2
10
2019
Statut:
ppublish
Résumé
While esters are frequently used as traditional electrophiles in substitution chemistry, their application in cross-coupling chemistry is still in its infancy. This work demonstrates that methyl esters can be used as coupling electrophiles in Ni-catalyzed Heck-type reactions through the challenging cleavage of the C(acyl)-O bond under relatively mild reaction conditions at either 80 or 100 °C. With the σ-Ni
Identifiants
pubmed: 31574201
doi: 10.1002/anie.201911372
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
18159-18164Subventions
Organisme : Natural Sciences and Engineering Research Council of Canada
Organisme : BASF Corporation
Informations de copyright
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
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