Recyclable nickel-catalyzed C–H/O–H dual functionalization of phenols with mandelic acids for the synthesis of 3-aryl benzofuran-2(3H)-ones under solvent-free conditions
Author:
Affiliation:
1. State Key Laboratory of Chemo/Biosensing and Chemometrics
2. College of Chemistry and Chemical Engineering
3. Hunan University
4. Changsha
5. P.R. China
6. Hunan Institute of Engineering
7. Xiangtan
Abstract
Cooperative catalysis: Green synthesis of 3-aryl benzofuran-2(3H)-ones under solvent-free conditions from phenols and mandelic acids using recyclable Ni(OTf)2 as a catalyst.
Funder
National Natural Science Foundation of China
Science and Technology Bureau, Changsha
Publisher
Royal Society of Chemistry (RSC)
Subject
Pollution,Environmental Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2019/GC/C9GC00305C
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3. Iridium-Catalyzed and Ligand-Controlled Carbonylative Synthesis of Flavones from Simple Phenols and Internal Alkynes
4. Palladium-Catalyzed Direct Annulation of Benzoic Acids with Phenols to Synthesize Dibenzopyranones
5. Selectivity Controlled Palladium-Catalyzed Carbonylative Synthesis of Propiolates and Chromenones from Phenols and Alkynes
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