Diastereoconvergent Synthesis of trans-5-Hydroxy-6-Substituted-2-Piperidinones by Addition–Cyclization–Deprotection Process
Author:
Affiliation:
1. Department of Chemistry and Institute of Biomedical Sciences, Fudan University, 220 Handan Road, Shanghai 200433, P.R. China
2. College of Science, Northwest Agriculture and Forestry University, Shaanxi Yangling 712100, P.R. China
Funder
National Natural Science Foundation of China
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol5020812
Reference62 articles.
1. Catalytic Asymmetric Synthesis
2. A General Approach to (5S,6R)-6-Alkyl-5-benzyloxy-2-piperidinones: Application to the Asymmetric Syntheses of Neurokinin Substance P Receptor Antagonist (−)-L-733,061 and (−)-Deoxocassine
3. Diastereoselective syntheses of 2-amino propargyl alcohols. Chiral building blocks for enantiopure amino γ-lactones and 5-hydroxy-piperidinone derivatives
4. Catalytic Asymmetric Vinylogous Mannich Reaction of N-(2-Thienyl)sulfonylimines
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