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Stereodivergent Photooxidative Synthesis of Cyclocariols A, B, and E from Ginsenoside Rg1 | Synapse

April 10, 2026

Stereodivergent Photooxidative Synthesis of Cyclocariols A, B, and E from Ginsenoside Rg1

Puntos clave

The aim is to develop a stereodivergent method for synthesizing cyclocariols A, B, and E from ginsenoside Rg1.
Employ visible-light-induced photooxidation
Conduct β-fragmentation/elimination cascade reactions
Focus on the transformation of ginsenoside Rg1 into cyclocariols
Successfully synthesized cyclocariols A, B, and E
Achieved high stereoselectivity in the reactions
Demonstrated the efficiency of visible-light-induced methods for triterpenoid synthesis

Resumen

We report a stereodivergent photooxidative synthesis of the 3,4-seco-dammarane triterpenoids cyclocariols A, B, and E from the commercially available ginsenoside Rg1. This study features a visible-light-induced β-fragmentation/elimination cascade reaction that...

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Authors

J

Jie Yuan

Sichuan University

S

Shaomin Fu

B

Bo Liu

Sichuan University

Journals

Organic & Biomolecular Chemistry

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Cite this study

Yuan et al. (Wed,) studied this question.

synapsesocial.com/papers/69d894ce6c1944d70ce05c2d — DOI: https://doi.org/10.1039/d6ob00346j