Chiral Bisphosphine-Catalyzed Asymmetric Staudinger/aza-Wittig Reaction: An Enantioselective Desymmetrizing Approach to Crinine-Type Amaryllidaceae Alkaloids
Author:
Affiliation:
1. School of Pharmaceutical Sciences, MOE Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology, Tsinghua University, Beijing 100084, China
Funder
Beijing Municipal Natural Science Foundation
Tsinghua University
National Natural Science Foundation of China
Tsinghua-Toyota Joint Research Fund
Publisher
American Chemical Society (ACS)
Link
https://pubs.acs.org/doi/pdf/10.1021/jacs.4c02755
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1. Amaryllidaceae and Sceletium alkaloids
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1. Chiral-Bisphosphine-Catalyzed Asymmetric Staudinger/Aza-Wittig Reaction: Development, Mechanism Study, and Synthetic Application;Synlett;2024-08-22
2. Benchmarking Methanophosphocines as Versatile PIII/PV Redox Organocatalysts;Advanced Synthesis & Catalysis;2024-08-13
3. Access to Crinine-Type Amaryllidaceae Alkaloids via an Asymmetric Staudinger/aza-Wittig Reaction Approach;Synfacts;2024-07-25
4. Palladium-Catalyzed Asymmetric Desymmetrization for the Simultaneous Construction of Chiral Phosphorus and Quaternary Carbon Stereocenters;Organic Letters;2024-07-05
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