J
Jincheng Mao
Researcher at Southwest Petroleum University
Publications - 251
Citations - 4148
Jincheng Mao is an academic researcher from Southwest Petroleum University. The author has contributed to research in topics: Catalysis & Aryl. The author has an hindex of 32, co-authored 225 publications receiving 3235 citations. Previous affiliations of Jincheng Mao include Dalian Institute of Chemical Physics & University of Basel.
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Highly efficient copper(0)-catalyzed Suzuki-Miyaura cross-coupling reactions in reusable PEG-400
TL;DR: Readingily available copper powder with K2CO3 as the base was extremely effective catalyst for Suzuki–Miyaura coupling reaction performed in PEG-400, which afforded almost quantitative coupling products of aryl iodides.
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Iron/Copper co-catalyzed synthesis of vinyl sulfones from sulfonyl hydrazides and alkyne derivatives.
TL;DR: A new approach to the selective synthesis of (E)-vinyl sulfones has been developed via a Fe/Cu co-catalyzed sulfonylation of arylpropiolic acid or phenylacetylene with sulfonyl hydrazides, comparable to the best results reported so far.
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Copper-catalyzed decarboxylative C(sp2)-C(sp3) coupling reactions via radical mechanism.
TL;DR: An example of copper-catalyzed decarboxylative C(sp(2))-C(3)) coupling reactions via C-H functionalization for the first time is developed and it is noteworthy that the catalytic system is very stable, low-cost, palladium-free, ligand-free and easily accessible.
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Highly efficient and practical phosphoramidite–copper catalysts for amination of aryl iodides and heteroaryl bromides with alkylamines and N(H)-heterocycles
TL;DR: In this article, a copper-catalyzed system using phosphoramidite as ligands was applied to N-arylation of alkylamines and N(H)-heterocycles with aryl iodides and heteroaryl bromides.
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Iron-catalyzed direct alkenylation of sp3(C–H) bonds via decarboxylation of cinnamic acids under ligand-free conditions
TL;DR: An example of highly efficient low-cost ferrocene-catalyzed decarboxylative C(sp2)–C(sp3) coupling reactions via C–H functionalization has been developed successfully and it is noteworthy that nanoparticles of Fe3O4 could be used as a reusable catalyst for 7 times in the absence of ligand.