Total Synthesis of Caesalpinnone A and Caesalpinflavan B: Evolution of a Concise Strategy
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, Baylor University, One Bear Place 97248, Waco, Texas 76798, United States
Funder
Division of Chemistry
Welch Foundation
Cancer Prevention and Research Institute of Texas
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/jacs.9b04472
Reference31 articles.
1. 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
2. Hydrogen Bonding Lowers Intrinsic Nucleophilicity of Solvated Nucleophiles
3. Contribution of the intramolecular hydrogen bond to the shift of the pKa value and the oxidation potential of phenols and phenolate anions
4. Potentiality of standardized extract and isolated flavonoids from Zuccagnia punctata for the treatment of respiratory infections by Streptococcus pneumoniae: In vitro and in vivo studies
5. Phenolic Constituents from Dalbergia cochinchinensis
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