Copper nanoparticles supported on 2-methoxy-1-phenylethanone-functionalized MCM-41: An efficient and recyclable catalyst for one-pot three-component C-S coupling reaction of aryl halides with benzyl bromide and thiourea

2019 ◽  
pp. e4853 ◽  
Author(s):  
Abdol R. Hajipour ◽  
Farzaneh Fakhari ◽  
Gholamreza Nabi Bidhendi
Keyword(s):  
Copper Nanoparticles ◽  
Benzyl Bromide ◽  
Coupling Reaction ◽  
Recyclable Catalyst ◽  
Aryl Halides ◽  
One Pot ◽  
Component C ◽  
Mcm 41

ChemInform Abstract: One-Pot Thioetherification of Aryl Halides with Thiourea and Benzyl Bromide in Water Catalyzed by Cu-Grafted Furfural Imine-Functionalized Mesoporous SBA-15.

ChemInform ◽  
2012 ◽  
Vol 43 (46) ◽  
pp. no-no
Author(s):  
John Mondal ◽  
Arindam Modak ◽  
Arghya Dutta ◽  
Sohini Basu ◽  
Shambhu Nath Jha ◽  
...  
Keyword(s):  
Benzyl Bromide ◽  
Aryl Halides ◽  
One Pot

A facile and convenient sequential homobimetallic catalytic approach towards β-methylstyrenes. A one-pot Stille cross-coupling/isomerization strategy

2014 ◽  
Vol 12 (22) ◽  
pp. 3735-3743 ◽  
Author(s):  
Sebastián O. Simonetti ◽  
Enrique L. Larghi ◽  
Teodoro S. Kaufman
Keyword(s):  
Double Bond ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Aryl Halides ◽  
One Pot ◽  
Cross Coupling Reaction

A one-pot approach towards β-methylstyrenes is reported. The transformation involves a Stille cross-coupling reaction of aryl halides with allyltributylstannane, followed by an in situ Pd-catalyzed double bond conjugative migration.

Synthesis of terminal arylacetylenes by a Stille coupling reaction catalysed by a MCM-41-supported bidentate phosphine palladium(O) complex

2008 ◽  
Vol 2008 (11) ◽  
pp. 615-618 ◽  
Author(s):  
Wenyan Hao ◽  
Yue Wang ◽  
Shouri Sheng ◽  
Mingzhong Cai
Keyword(s):  
Aqueous Medium ◽  
Palladium Catalyst ◽  
Basic Problem ◽  
Coupling Reaction ◽  
Aryl Halides ◽  
Stille Coupling ◽  
Bidentate Phosphine ◽  
Stille Coupling Reaction ◽  
High Yields ◽  
Mcm 41

A variety of terminal arylacetylenes have been conveniently synthesised in good to high yields by Stille coupling of aryl halides with ethynyltributylstannane catalysed by a MCM-41-supported bidentate phosphine palladium(O) complex in an aqueous medium and under air. Our system not only avoids the requirement for water-free and oxygen-free conditions, but also solves the basic problem of palladium catalyst reuse.

ChemInform Abstract: One-Pot Aromatic Amination Based on Carbon-Nitrogen Coupling Reaction Between Aryl Halides and Azido Compounds.

ChemInform ◽  
2012 ◽  
Vol 43 (27) ◽  
pp. no-no
Author(s):  
Toshihide Maejima ◽  
Yutaka Shimoda ◽  
Kei Nozaki ◽  
Shigeki Mori ◽  
Yoshinari Sawama ◽  
...  
Keyword(s):  
Coupling Reaction ◽  
Aryl Halides ◽  
One Pot ◽  
Nitrogen Coupling
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