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Total Synthesis of (±)- and (+)-Euphohyrisnoid A.

PubMed
Authors: Ye ZH, Ao QQ, Peng YC, Liu X, Lin X, Li CC

Year

2026

Paper ID

9743

Status

Peer-reviewed

Abstract Read

~2 min

Abstract Words

80

Citations

5

Abstract

The first total synthesis of (±)- and (+)-euphohyrisnoid A, a highly rearranged lathyrane diterpenoid with a new [5-7-6-6] tetracyclic core, was accomplished. The synthesis was strategically guided by a mild intramolecular Diels-Alder (IMDA) reaction, which efficiently constructed the pivotal bicyclo[2.2.2] ring system with high diastereoselectivity. This outcome experimentally validated prior quantum mechanical calculations. The IMDA precursor was assembled efficiently via a Tsuji-Trost reaction. The desired seven stereocenters, including two quaternary stereocenters in the final product, were constructed diastereoselectively.

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  • The first total synthesis of (±)- and (+)-euphohyrisnoid A, a highly rearranged lathyrane diterpenoid with a new [5-7-6-6] tetracyclic core, was accomplished.

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External citation index: OpenAlex citation signal • updated 2026-10-22 12:25:36

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