Ni-Catalyzed Carbon–Carbon Bond-Forming Reductive Amination-Reference-Cited by-同舟云学术

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Ni-Catalyzed Carbon–Carbon Bond-Forming Reductive Amination

Published:2018-02-01 Issue:6 Volume:140 Page:2292-2300
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Heinz Christoph¹,Lutz J. Patrick¹,Simmons Eric M.²^ORCID,Miller Michael M.³,Ewing William R.³,Doyle Abigail G.¹^ORCID

Affiliation:

1. Department of Chemistry, Princeton University, Princeton, New Jersey 08544, United States

2. Chemical and Synthetic Development, Bristol-Myers Squibb, New Brunswick, New Jersey 08903, United States

3. Discovery Chemistry, Bristol-Myers Squibb, P.O. Box 5400, Princeton, New Jersey 08543-5400, United States

Funder

Schweizerischer Nationalfonds zur F?rderung der Wissenschaftlichen Forschung

Division of Graduate Education

Bristol-Myers Squibb

National Institute of General Medical Sciences

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.7b12212

Reference73 articles.

1. The Medicinal Chemist’s Toolbox: An Analysis of Reactions Used in the Pursuit of Drug Candidates

2. An overview of the key routes to the best selling 5-membered ring heterocyclic pharmaceuticals

3. An overview of the synthetic routes to the best selling drugs containing 6-membered heterocycles

4. Reductive Amination of Aldehydes and Ketones with Sodium Triacetoxyborohydride. Studies on Direct and Indirect Reductive Amination Procedures1

5. A Review on the Use of Sodium Triacetoxyborohydride in the Reductive Amination of Ketones and Aldehydes

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