Enantioselective Phosphine-Catalyzed Trimerization of γ-Aryl-3-butynoates via Isomerization/[3 + 2] Cyclization/Michael Addition Cascade
Author:
Affiliation:
1. Department of Chemistry, Zhejiang Sci-Tech University, Hangzhou, Zhejiang 310018, P. R. China
2. College of Biological, Chemical Sciences and Engineering, Jiaxing University, Jiaxing, Zhejiang 314001, P. R. China
Funder
Zhejiang Sci-Tech University
National Natural Science Foundation of China
Natural Science Foundation of Zhejiang Province
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.1c02197
Reference42 articles.
1. Reactions of Electron-Deficient Alkynes and Allenes under Phosphine Catalysis
2. Nucleophilic Phosphine Organocatalysis
3. Engaging Zwitterions in Carbon−Carbon and Carbon−Nitrogen Bond-Forming Reactions: A Promising Synthetic Strategy
4. Multifunctional Chiral Phosphine Organocatalysts in Catalytic Asymmetric Morita−Baylis−Hillman and Related Reactions
5. Phosphine catalysis of allenes with electrophiles
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