Sequential Phosphine-Catalyzed [4 + 2] Annulation of β′-Acetoxy Allenoates: Enantioselective Synthesis of 3-Ethynyl-Substituted Tetrahydroquinolines
Author:
Affiliation:
1. State Key Laboratory and Institute of Elemento-organic Chemistry, College of Chemistry, Nankai University, Tianjin 300071, China
2. Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin 300071, China
Funder
National Natural Science Foundation of China
Natural Science Foundation of Tianjin City
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b00130
Reference69 articles.
1. Reactions of Electron-Deficient Alkynes and Allenes under Phosphine Catalysis
2. Nucleophilic Phosphine Organocatalysis
3. Phosphine-triggered synthesis of functionalized cyclic compounds
4. Enantioselective catalysis and complexity generation from allenoates
5. Development of asymmetric phosphine-promoted annulations of allenes with electron-deficient olefins and imines
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