Facile Reduction of Amides Using Nickel Catalysis: Reduction of 12‐Aminododecanolactam

Author:

Simmons Bryan J.,Ramirez Melissa,Garg* Neil K.,Shimakawa Tsukasa,Hagiwara Koichi,Inoue Masayuki

Publisher

Wiley

Reference57 articles.

1. Department of Chemistry and Biochemistry University of California Los Angeles California 90095 United States. E‐mail:neilgarg@chem.ucla.edu. ORCID: 0000‐0002‐7793‐2629. The authors are grateful to the University of California Los Angeles the UCLA Cota Robles Fellowship Program (M.R.) NIGMS (M.R. Diversity Supplement for R01 GM117016) and the NSF (B.J.S. DGE‐1144087). These studies were also supported by shared instrumentation grants from the NSF (CHE‐1048804) and the National Center for Research Resources (S10RR025631).

2. Conversion of amides to esters by the nickel-catalysed activation of amide C–N bonds

3. Nickel-catalysed Suzuki–Miyaura coupling of amides

4. A two-step approach to achieve secondary amide transamidation enabled by nickel catalysis

5. Nickel-Catalyzed Alkylation of Amide Derivatives

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