Recent Advances in the Palladium Catalyzed Suzuki–Miyaura Cross-Coupling Reaction in Water

The palladium-catalyzed Suzuki–Miyaura cross-coupling reaction of organic halides with boronic acids is one of the most versatile methods for the synthesis of biaryls. Green chemistry is a rapidly developing new field that provides us a proactive avenue for the sustainable development of future scie...

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Bibliographic Details
Published in:Catalysis letters Vol. 146; no. 4; pp. 820 - 840
Main Authors: Chatterjee, Anamitra, Ward, Thomas R.
Format: Journal Article
Language:English
Published: New York Springer US 01.04.2016
Springer
Springer Nature B.V
Subjects:
Catalysis
Chemical industry
Chemical reactions
Chemical synthesis
Chemical technology
Chemistry
Chemistry and Materials Science
Cross coupling
Green chemistry
Green technology
Halides
Industrial Chemistry/Chemical Engineering
Literature reviews
Organic chemistry
Organometallic Chemistry
Palladium
Physical Chemistry
Sustainable development
Aqueous catalysis
Palladium
Green chemistry
Cross-coupling
Sustainable chemistry
ISSN:1011-372X, 1572-879X
Online Access:Get full text
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Summary:The palladium-catalyzed Suzuki–Miyaura cross-coupling reaction of organic halides with boronic acids is one of the most versatile methods for the synthesis of biaryls. Green chemistry is a rapidly developing new field that provides us a proactive avenue for the sustainable development of future science and technologies. When designed properly, clean chemical technology can be developed in water as a reaction medium. The technologies generated from such green chemistry endeavours may often be cheaper and more profitable. This review covers the literature on palladium-catalysed the Suzuki–Miyaura cross-coupling reaction in water. Graphical Abstract
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ISSN:1011-372X
1572-879X
DOI:10.1007/s10562-016-1707-8