Efficient synthesis of tetrasubstituted 2,3-allenoates and preliminary studies on bioactivities
Author:
Affiliation:
1. Research Center for Molecular Recognition and Synthesis
2. Department of Chemistry
3. Fudan University
4. Shanghai 200433
5. P. R. China
Abstract
A general and highly efficient straightforward protocol for the preparation of tetrasubstituted 2,3-allenoates through a palladium-catalyzed coupling reaction of 3-alkoxycarbonyl propargylic carbonates and boronic acids with commercially available tri(o-tolyl)phosphine as a ligand has been developed.
Funder
National Natural Science Foundation of China
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2019/QO/C8QO01202D
Reference85 articles.
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