Issue 68, 2014

Palladacycle-catalyzed Suzuki–Miyaura reaction of aryl/heteroaryl halides with MIDA boronates in EtOH/H2O or H2O

Abstract

With good to excellent yields, a series of mono- or diheteroaryl compounds were synthesized via the palladacycle-catalyzed Suzuki–Miyaura reaction of various N-methyliminodiacetic acid (MIDA) boronates with aryl/heteroaryl halides in EtOH/H2O or H2O.

Graphical abstract: Palladacycle-catalyzed Suzuki–Miyaura reaction of aryl/heteroaryl halides with MIDA boronates in EtOH/H2O or H2O

Supplementary files

Article information

Article type
Paper
Submitted
11 May 2014
Accepted
06 Aug 2014
First published
07 Aug 2014

RSC Adv., 2014,4, 36262-36266

Author version available

Palladacycle-catalyzed Suzuki–Miyaura reaction of aryl/heteroaryl halides with MIDA boronates in EtOH/H2O or H2O

Y. Li, J. Wang, Z. Wang, M. Huang, B. Yan, X. Cui, Y. Wu and Y. Wu, RSC Adv., 2014, 4, 36262 DOI: 10.1039/C4RA07486F

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