An efficient and new protocol for phosphine-free Suzuki coupling reaction using palladium-encapsulated and air-stable MIDA boronates in an aqueous medium-Reference-Cited by-同舟云学术

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

Published:2014 Issue:53 Volume:4 Page:28148-28155
ISSN:2046-2069
Container-title:RSC Adv.
language:en
Short-container-title:RSC Adv.

Author:

Mendes da Silva Joaquim Fernando¹²³,Yepes Perez Andres Felipe¹²³⁴⁵,Pinto de Almeida Natália¹²³

Affiliation:

1. Instituto de Química

2. Universidade Federal do Rio de Janeiro

3. Rio de Janeiro, Brazil

4. Facultad de Ciencias Físicas Exactas y Naturales Universidad de Santander (UDES). Centro Investigación en Ciencias Químicas y Tecnologías Sostenibles-QUIMISOST Cidade Universitária

5. Campus Lagos del Cacique Bucaramanga

Abstract

A simple methodology for Suzuki–Miyaura cross-coupling reactions using microencapsulated palladium and (het)aryl MIDA boronates in water–alcohol under phosphine-free conditions was developed.

Funder

CoordenaÃ§Ã£o de AperfeiÃ§oamento de Pessoal de NÃvel Superior

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/RA/C4RA03586K

Reference94 articles.

1. Cross-Coupling Reactions Of Organoboranes: An Easy Way To Construct CC Bonds (Nobel Lecture)

2. Cross-coupling Reactions of Organoboranes: An Easy Method for C–C Bonding

3. Nanocatalysts for Suzuki cross-coupling reactions