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Updated: May 20, 2026

A Customizable Approach for the Enzymatic Production and Purification of Diterpenoid Natural Products
Published on: October 4, 2019
Two concise enantioselective total syntheses of (-)-glabrescol implicate alternative biosynthetic pathways starting
Peng Yang1, Pei-Fang Li, Jin Qu
1State Key Laboratory of Elemento-Organic Chemistry, Nankai University, Tianjin, 300071, China.
Abstract:
The C(2)-symmetric (-)-glabrescol was synthesized in two steps from (10S,11R)-dihydroxy-10,11-dihydrosqualene or squalene with 50% or 10% overall yields, respectively. These highly efficient and biomimetic syntheses employed a base-promoted middle-to-terminal double epoxide-opening cascade, which constructs the five tetrahydrofuran rings in glabrescol in one operation.
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