Nickel-Catalyzed Enantioselective Reductive Arylation of Common Ketones
Author:
Affiliation:
1. State Key Laboratory of Chemical Oncogenomics, School of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate School, 2199 Lishui Road, Nanshan District, Shenzhen 518055, China
Funder
Shenzhen Bay Laboratory
National Natural Science Foundation of China
Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, Shanghai Jiao Tong University
Peking University Shenzhen Graduate School
Publisher
American Chemical Society (ACS)
Link
https://pubs.acs.org/doi/pdf/10.1021/jacs.4c02818
Reference61 articles.
1. Catalytic Asymmetric Organozinc Additions to Carbonyl Compounds
2. Asymmetric Synthesis of Tertiary Alcohols and α-Tertiary Amines via Cu-Catalyzed C−C Bond Formation to Ketones and Ketimines
3. Recent Advances in Catalytic Asymmetric Synthesis of Tertiary Alcohols via Nucleophilic Addition to Ketones
4. ASYMMETRIC NUCLEOPHILIC ADDITION TO KETONES AND KETIMINES AND CONJUGATE ADDITION REACTIONS
5. Recent advances in the asymmetric catalytic construction of oxa-quaternary carbon centers
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1. A General Enantioselective α-Alkyl Amino Acid Derivatives Synthesis Enabled by Cobalt-Catalyzed Reductive Addition;Journal of the American Chemical Society;2024-09-12
2. Enantioselective Desymmetrization of 1,3‐Dicarbonyl Compounds through Transition‐Metal‐Catalyzed Intramolecular Cyclization Reactions;ChemCatChem;2024-08-22
3. Enantioselective Synthesis of Tertiary Alcohols by a Nickel-Catalyzed Reductive Arylation of Ketones;Synfacts;2024-07-25
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