Issue 6, 2002
From the journal:

Chemical Communications

Ultrasound promoted Suzuki cross-coupling reactions in ionic liquid at ambient conditions

R. Rajagopal,a   Dilip V. Jarikotea  and  K. V. Srinivasan*a  

* Corresponding authors

a Organic Chemistry; Technology Division, National Chemical Laboratory, Pune, India
E-mail: kvsri@dalton.ncl.res.in

Abstract

Palladium catalyzed Suzuki cross-coupling reactions of halobenzenes including chlorobenzenes with phenylboronic acid have been achieved at ambient temperature (30 °C) in the absence of a phosphine ligand using the ionic liquid 1,3-di-n-butylimidazolium tetrafluoroborate [bbim][BF4] with methanol as co-solvent under ultrasonic irradiation.

Graphical abstract: Ultrasound promoted Suzuki cross-coupling reactions in ionic liquid at ambient conditions

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Article information

DOI
https://doi.org/10.1039/B111271F
Article type
Communication
Submitted
11 Dec. 2001
Accepted
12 Febr. 2002
First published
22 Febr. 2002

Chem. Commun., 2002, 616-617

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Ultrasound promoted Suzuki cross-coupling reactions in ionic liquid at ambient conditions

R. Rajagopal, D. V. Jarikote and K. V. Srinivasan, Chem. Commun., 2002, 616 DOI: 10.1039/B111271F

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