Related Experiment Video
Updated: Sep 14, 2025

A Customizable Approach for the Enzymatic Production and Purification of Diterpenoid Natural Products
Published on: October 4, 2019
Bioinspired Total Synthesis of (+)-α-Tocopherol
Jiaxin Cheng1, Zhigang Liu1, Ding Liu1
1Engineering Center of Catalysis and Synthesis for Chiral Molecules, Department of Chemistry, Fudan University, Shanghai 200433, China.
None:
The bioinspired total synthesis of α-tocopherol was achieved using a late-stage organocatalytic halo-cycloetherification reaction to construct the critical 2,2-disubstituted chroman scaffold stereoselectively. The reactivity and stereoselectivity of this reaction were studied under both batch and continuous-flow conditions. This method offers a reliable strategy for synthesizing C2-functionalized chromans, key chiral building blocks for natural product synthesis and pharmaceuticals.
Related Concept Videos
Biosynthesis of Lipids
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Alkylation of β-Diester Enolates: Malonic Ester Synthesis
Cyclohexenones via Michael Addition and Aldol Condensation: The Robinson Annulation
Alkylation of β-Ketoester Enolates: Acetoacetic Ester Synthesis
ATP and Macromolecule Synthesis
Most macromolecules are composed of single subunits, or building blocks, called monomers. The monomers combine with each other using covalent bonds to form larger molecules known as polymers.
Conversion of...

