M
Mingzhong Cai
Researcher at Jiangxi Normal University
Publications - 457
Citations - 3876
Mingzhong Cai is an academic researcher from Jiangxi Normal University. The author has contributed to research in topics: Catalysis & Palladium. The author has an hindex of 30, co-authored 436 publications receiving 3363 citations. Previous affiliations of Mingzhong Cai include Hangzhou University.
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A phosphine-free carbonylative cross-coupling reaction of aryl iodides with arylboronic acids catalyzed by immobilization of palladium in MCM-41
TL;DR: In this paper, a phosphine-free heterogeneous carbonylative cross-coupling of aryl iodides with aryboronic acids under an atmospheric pressure of carbon monoxide was achieved in anisole at 80 °C in the presence of a 3-(2-aminoethylamino)propyl-functionalized MCM-41-immobilized palladium(II) complex.
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The first heterogeneous carbonylative Stille coupling of organostannanes with aryl iodides catalyzed by MCM-41-supported bidentate phosphine palladium(0) complex
TL;DR: In this paper, the first heterogeneous Stille coupling reaction of organostannanes with aryl iodides under an atmospheric pressure of carbon monoxide has been achieved in DMF at 80 °C in the presence of a catalytic amount of an MCM-41-supported bidentate phosphine palladium(0) complex.
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Practical Oxidative Homo‐ and Heterocoupling of Terminal Alkynes Catalyzed by Immobilized Copper in MCM‐41
TL;DR: In this article, a 3-(2-aminoethylamino)propyl-functionalized MCM-41-immobilized copper(I) complex was used for CH2Cl2 at 25 °C, yielding a variety of symmetrical and unsymmetrical 1,4-disubstituted 1,3-diynes.
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Recyclable heterogeneous palladium-catalyzed carbon–carbon coupling polycondensations toward highly purified conjugated polymers
TL;DR: In this paper, a bidentate phosphino-modified magnetic nanoparticles-anchored palladium complex (PdCl2-Fe3O4@SiO2-2P) was developed as a clean and efficient heterogeneous catalyst for the carbon-carbon coupling polycondensations.
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Carbonylative Suzuki–Miyaura Coupling of Arylboronic Acids with Aryl Iodides Catalyzed by the MCM-41-Supported Bidentate Phosphane Palladium(II) Complex
TL;DR: In this article, the first heterogeneous Suzuki-Miyaura cross-coupling reaction of arylboronic acids with aryls iodides under an atmospheric pressure of carbon monoxide has been achieved in anisole at 80 °C in the presence of a catalytic amount of an MCM-41-supported bidentate phosphane palladium(II) complex.