Simplified Modular Access to Enantiopure 1,2-Aminoalcohols via Ni-Electrocatalytic Decarboxylative Arylation-Reference-Cited by-同舟云学术

Simplified Modular Access to Enantiopure 1,2-Aminoalcohols via Ni-Electrocatalytic Decarboxylative Arylation

Published:2024-02-22 Issue:9 Volume:146 Page:6209-6216
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Sun Jiawei¹,Endo Hirofumi¹,Emmanuel Megan A.²^ORCID,Oderinde Martins S.³^ORCID,Kawamata Yu¹^ORCID,Baran Phil S.¹^ORCID

Affiliation:

1. Department of Chemistry, Scripps Research, 10550 North Torrey Pines Road, La Jolla, California 92037, United States

2. Chemical Process Development, Bristol Myers Squibb, 1 Squibb Drive, New Brunswick, New Jersey 08901, United States

3. Small Molecule Drug Discovery, Bristol Myers Squibb Research & Early Development, Route 206 & Province Line Road, Princeton, New Jersey 08543, United States

Funder

Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences

Bill and Melinda Gates Foundation

Japan Society for the Promotion of Science

National Science Foundation

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.3c14119

Reference62 articles.

1. The Synthesis of Vicinal Amino Alcohols

2. Diastereoselective synthesis of vicinal amino alcohols

3. Biocatalytic approaches towards the stereoselective synthesis of vicinal amino alcohols

4. Catecholamine Derivatives: Natural Occurrence, Structural Diversity, and Biological Activity

5. Econazole

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