Total Synthesis of Caesalpinnone A
Author:
Affiliation:
1. Shaanxi Key Laboratory of Natural Products and Chemical Biology, College of Chemistry and Pharmacy, Northwest A&F University, 3 Taicheng Road, Yangling 712100, Shaanxi, P. R. China
Funder
Ministry of Education of the People's Republic of China
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/acs.orglett.9b04276
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4. dMcRae, J. M.; Yang, Q.; Crawford, R. J.; Palombo, E. A. In Flavonoids: Biosynthesis, Biological Effects and Dietary Sources; Keller, R. B., Eds. Nova Science Publishers: New York, 2009; pp 291–299.
5. Four Hybrid Flavan–Chalcones, Caesalpinnone A Possessing a 10,11-Dioxatricyclic [5.3.3.01,6]Tridecane-Bridged System and Caesalpinflavans A–C from Caesalpinia enneaphylla
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