Nickel-Catalyzed Asymmetric Hydrogenation of γ-Keto Acids, Esters, and Amides to Chiral γ-Lactones and γ-Hydroxy Acid Derivatives
Author:
Affiliation:
1. Key Laboratory of Radiopharmaceuticals, College of Chemistry, Beijing Normal University, Beijing 100875, China
2. Research Institute of Petroleum Processing, SINOPEC, Beijing 100083, China
Funder
Natural Science Foundation of Beijing Municipality
National Natural Science Foundation of China
Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.2c00826
Reference46 articles.
1. Synthese und biologische Aktivität von α-Methylen-γ-butyrolactonen
2. A short synthesis of (+)-harzialactone A and (R)-(+)-4-hexanolide via proline-catalyzed sequential α-aminooxylation and Horner–Wadsworth–Emmons olefination of aldehydes
3. The Renaissance of α-Methylene-γ-butyrolactones: New Synthetic Approaches
4. Analysis of the fingerprint profile of bioactive constituents of traditional Chinese medicinal materials derived from animal bile using the HPLC–ELSD and chemometric methods: An application of a reference scaleplate
5. Efficient Synthesis of γ-Lactones via Gold-Catalyzed Tandem Cycloisomerization/Oxidation
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