Tridentate Hydroxy-Functionalised MCM-41-Immobilised Copper(I) Complex as an Efficient and Recyclable Catalyst for Coupling of Aryl Iodides with Thiols

2015 ◽  
Vol 39 (10) ◽  
pp. 612-616 ◽  
Author(s):  
Fang Yao ◽  
Rongli Zhang ◽  
Yichao Wu ◽  
Mingzhong Cai
Keyword(s):  
Recyclable Catalyst ◽  
Aryl Iodides ◽  
Mcm 41

MCM-41-immobilized 1,10-phenanthroline–copper(i) complex: a highly efficient and recyclable catalyst for the coupling of aryl iodides with aliphatic alcohols

RSC Advances ◽  
2016 ◽  
Vol 6 (88) ◽  
pp. 85186-85193 ◽  
Author(s):  
Yang Lin ◽  
Mingzhong Cai ◽  
Zhiqiang Fang ◽  
Hong Zhao
Keyword(s):  
Practical Method ◽  
Recyclable Catalyst ◽  
Aliphatic Alcohols ◽  
Highly Efficient ◽  
Aryl Iodides ◽  
Alkyl Ethers ◽  
Mcm 41

A practical method for the synthesis of aryl alkyl ethers has been developed by heterogeneous Cu-catalyzed C–O coupling.

Amine functionalized MCM-41: an efficient heterogeneous recyclable catalyst for the synthesis of quinazoline-2,4(1H,3H)-diones from carbon dioxide and 2-aminobenzonitriles in water

2014 ◽  
Vol 4 (6) ◽  
pp. 1608-1614 ◽  
Author(s):  
Deepak B. Nale ◽  
Surjyakanta Rana ◽  
Kulamani Parida ◽  
Bhalchandra M. Bhanage
Keyword(s):  
Carbon Dioxide ◽  
Recyclable Catalyst ◽  
Efficient Catalyst ◽  
Amine Functionalized ◽  
Covalently Linked ◽  
Mcm 41

Covalently linked amine functionalized MCM-41 was investigated as an efficient catalyst for the synthesis of various quinazoline-2,4(1H,3H)-dione derivatives from 2-aminobenzonitriles and carbon dioxide in water.

Highly para-selective C‒H alkylation of unactivated arenes with α-aryl-α-diazoesters catalyzed by gold(I) immobilized on MCM-41

2019 ◽  
Vol 44 (3-4) ◽  
pp. 174-180 ◽  
Author(s):  
Yingying Du ◽  
Fang Yao ◽  
Mingzhong Cai
Keyword(s):  
Recyclable Catalyst ◽  
Benzene Derivatives ◽  
Mild Conditions ◽  
Alkylation Of Benzene ◽  
Mcm 41 ◽  
Electron Withdrawing Substituents

The heterogeneous gold(I)-catalyzed highly para-selective C(sp2)–H bond alkylation of benzene derivatives with α-aryl-α-diazoesters possessing electron-withdrawing substituents on the aryl rings are achieved. The reactions proceed under mild conditions in good to excellent yields by using an MCM-41-anchored diphenylphosphine gold(I) complex [MCM-41-PPh2-AuOTf] as a recyclable catalyst.

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