Title of article :
FeCl3/ AgOTf Catalyzed Hydroarylation Reactions of Aryl-substitutedAlkynes with Different Electron-rich Arenes
Author/Authors :
Rahman, Md. Ataur Department of Chemistry - Jahangirnagar University - Savar - Dhaka-1342, Bangladesh , Kitamura, Tsugio Department of Chemistry and Applied Chemistry - Graduate School of Science and Engineering - Saga University - Honjo-machi - Saga - 840-8502, Japan
Pages :
11
From page :
13
To page :
23
Abstract :
There are many synthetic methods for the direct formation of carbon-carbon bond between arenes and alkynes. Metal-catalyzed hydroarylation reaction is one of the synthetic methods for the direct formation of new carbon-carbon bond between arenes and alkynes. The hydroarylation reaction of aryl-substituted alkynes with arenes proceeded smoothly in the presence of FeCl3/AgOTf catalyst system in a mixed solvent of trifluoroacetic acid and dichloromethane at 30ºC and yielded aryl-substituted alkenes in moderate to high yields. Electron rich arenes gave high yields whereas the relatively less electron rich arenes gave norminal yields.
Keywords :
FeCl3/AgOTf catalyst , hydroarylation , alkynes , arenes , arylalkenes
Journal title :
Malaysian Journal of Chemistry
Serial Year :
2017
Full Text URL :
Record number :
2597851
Link To Document :
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