Reductive Arylation of Amides via a Nickel‐Catalyzed Suzuki–Miyaura‐Coupling and Transfer‐Hydrogenation Cascade-Reference-Cited by-同舟云学术

Reductive Arylation of Amides via a Nickel‐Catalyzed Suzuki–Miyaura‐Coupling and Transfer‐Hydrogenation Cascade

Published:2020-11-30 Issue:5 Volume:60 Page:2472-2477
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Boit Timothy B.¹,Mehta Milauni M.¹,Kim Junyong¹,Baker Emma L.¹,Garg Neil K.¹^ORCID

Affiliation:

1. Department of Chemistry and Biochemistry University of California, Los Angeles Los Angeles CA 90095 USA

Funder

National Institute of General Medical Sciences

Tobacco-Related Disease Research Program

Division of Graduate Education

Division of Chemistry

National Center for Research Resources

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.202012048

Reference142 articles.

1. N-methoxy-n-methylamides as effective acylating agents

2. One‐pot Unsymmetrical Ketone Synthesis Employing a Pyrrole‐Bearing Formal Carbonyl Dication Linchpin Reagent

3. One-pot Unsymmetrical Ketone Synthesis Employing a Pyrrole-Bearing Formal Carbonyl Dication Linchpin Reagent

4. For representative reviews and publications on the non-decarbonylative transition metal-catalyzed cross-coupling of carboxylic acid derivatives see:

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