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

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Authors: Zhanhong Ye, Qiao-Qiao Ao, Yang-Chao Peng, Xin Liu, X. Sheldon Lin, Chuang‐Chuang Li
Cited by: 4
References: 50

Abstract

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.

Fields of Study & Subjects

Bioactive Natural Diterpenoids Research Biological Activity of Diterpenoids and Biflavonoids Plant-based Medicinal Research

Publication details

Journal / source
Journal of the American Chemical Society
Publisher
American Chemical Society (ACS)
Volume
148
Issue
6
Pages
5940–5945
Publication date
6 February 2026
Language
EN