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Updated: Jan 9, 2026

Biosynthesis of a Flavonol from a Flavanone by Establishing a One-pot Bienzymatic Cascade
Published on: August 14, 2019
Chemoenzymatic synthesis of the cardenolide rhodexin A and its aglycone sarmentogenin
Fuzhen Song1, Mengmeng Zheng2, Dongkai Wang1
1Engineering Research Center of Organosilicon Compounds & Materials (Ministry of Education), Hubei Key Lab on Organic and Polymeric OptoElectronic Materials, College of Chemistry and Molecular Sciences, The Institute for Advanced Studies, TaiKang Center for Life and Medical Sciences and State Key Laboratory of Metabolism and Regulation in Complex Organisms, Wuhan University, Wuhan, 430072, China.
Abstract:
Herein, we report a concise chemoenzymatic synthesis of the cardenolide rhodexin A in 9 steps and the first protecting-group-free synthesis of its aglycone sarmentogenin in 7 steps from 17-deoxycortisone. The synthesis features a scalable enzymatic C14-H α-hydroxylation, a Bestmann ylide-enabled one-step construction of the butenolide motif, a late stage Mukaiyama hydration, and a stereoselective C11 carbonyl reduction.
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