Issue 45, 2016
From the journal:

Organic & Biomolecular Chemistry

Asymmetric total synthesis of hedyosumin E aglycon, 7,10-epoxyhedyosminolide and ent-zedolactone A†‡

Xuan Wang,§a   Wang-Bin Sun,§ab   Jian-Ping Zou,b   Guo-Qiang Lina  and  Bing-Feng Sun*a  

* Corresponding authors

a CAS Key Laboratory of Synthetic Chemistry of Natural Substances, Shanghai Institute of Organic Chemistry, 345 Lingling Road, Shanghai 200032, China
E-mail: bfsun@sioc.ac.cn

b Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry and Chemical Engineering, Soochow University, Suzhou, Jiangsu 215123, China

Abstract

The asymmetric total syntheses of hedyosumin E aglycon, 7,10-epoxyhedyosminolide and ent-zedolactone A were realized, with the first two being achieved for the first time.

Graphical abstract: Asymmetric total synthesis of hedyosumin E aglycon, 7,10-epoxyhedyosminolide and ent-zedolactone A

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Article information

DOI
https://doi.org/10.1039/C6OB02179D
Article type
Communication
Submitted
06 Oct 2016
Accepted
24 Oct 2016
First published
24 Oct 2016

Org. Biomol. Chem., 2016,14, 10581-10584

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Asymmetric total synthesis of hedyosumin E aglycon, 7,10-epoxyhedyosminolide and ent-zedolactone A

X. Wang, W. Sun, J. Zou, G. Lin and B. Sun, Org. Biomol. Chem., 2016, 14, 10581 DOI: 10.1039/C6OB02179D

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