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Nickel-catalysed Suzuki–Miyaura cross-coupling reactions of aryl halides with arylboronic acids in ionic liquids

Paper ID Volume ID Publish Year Pages File Format Full-Text
49922 46773 2015 4 PDF Available
Title
Nickel-catalysed Suzuki–Miyaura cross-coupling reactions of aryl halides with arylboronic acids in ionic liquids
Abstract

•Excellent green catalytic system for the nickel-catalysed Suzuki reaction•Efficient yield for aryl halides with arylboronic acids in ionic liquids•Large amount of synthesis using a simple and economical process

An efficient strategy for the nickel-catalysed synthesis of biaryls and terphenyls has been developed in environmentally-friendly reaction media. In the presence of β-diketone and PPh3 ligands, Ni(TFA)2 acted as an effective catalyst for the Suzuki–Miyaura cross-coupling of aryl halides and arylboronic acids in an ionic liquid solution. Biaryls and terphenyls were obtained in good yields under this catalytic system.

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Keywords
XPHZZGJWRNBLOV-UHFFFAOYSA-NNickel-catalysed; Ionic liquid; Suzuki–Miyaura cross-coupling; Biaryls
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Nickel-catalysed Suzuki–Miyaura cross-coupling reactions of aryl halides with arylboronic acids in ionic liquids
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Publisher
Database: Elsevier - ScienceDirect
Journal: Catalysis Communications - Volume 58, 5 January 2015, Pages 154–157
Authors
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Subjects
Physical Sciences and Engineering Chemical Engineering Catalysis
Get Full-Text Now
Don't Miss Today's Special Offer
Price was $35.95
You save - $31
Price after discount Only $4.95
100% Money Back Guarantee
Full-text PDF Download
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