Diastereoselective α-Hydroxylation of N-tert-Butanesulfinyl Imidates and N′-tert-Butanesulfinyl Amidines with Molecular Oxygen
Author:
Affiliation:
1. Key Laboratory of Plant Resources and Chemistry of Arid Zones, Xinjiang Technical Institute of Physics & Chemistry, Chinese Academy of Sciences, Urumqi 830011, China
2. University of Chinese Academy of Sciences, Beijing 100049, China
Funder
National Natural Science Foundation of China
Central Committee of the Communist Party of China
Xinjiang Technical Institute of Physics and Chemistry
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.8b00178
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5. Enantioselective α-Hydroxylation by Modified Salen-Zirconium(IV)-Catalyzed Oxidation of β-Keto Esters
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