Issue 53, 2014

An efficient and new protocol for phosphine-free Suzuki coupling reaction using palladium-encapsulated and air-stable MIDA boronates in an aqueous medium

Abstract

A simple methodology that uses a system based on polyurea microencapsulated palladium (PdEnCat 30™) and aryl or (2-pyridyl) MIDA boronates for Suzuki–Miyaura cross-coupling reactions of (hetero)aryl halides in water–alcohol under phosphine-free conditions was developed.

Graphical abstract: An efficient and new protocol for phosphine-free Suzuki coupling reaction using palladium-encapsulated and air-stable MIDA boronates in an aqueous medium

Article information

Article type
Paper
Submitted
20 Apr 2014
Accepted
13 Jun 2014
First published
16 Jun 2014

RSC Adv., 2014,4, 28148-28155

Author version available

An efficient and new protocol for phosphine-free Suzuki coupling reaction using palladium-encapsulated and air-stable MIDA boronates in an aqueous medium

J. F. Mendes da Silva, A. F. Yepes Perez and N. Pinto de Almeida, RSC Adv., 2014, 4, 28148 DOI: 10.1039/C4RA03586K

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