Stereoselective construction of a key hydroindole precursor of epidithiodiketopiperazine (ETP) natural products
Author:
Affiliation:
1. Shanghai Key Laboratory of Green Chemistry and Chemical Process
2. Department of Chemistry
3. East China Normal University
4. Shanghai 200062, P. R. China
5. State Key Laboratory of Elemento-organic Chemistry
Abstract
The functionalized hexahydroindole scaffold of ETPs was constructed by an asymmetric strategy involving a diastereoselective inverse electron-demand Diels–Alder (IEDDA) reaction.
Publisher
Royal Society of Chemistry (RSC)
Subject
Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis
Link
http://pubs.rsc.org/en/content/articlepdf/2014/CC/C4CC04148H
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