Suzuki-Miyaura cross-coupling reactions in aqueous media: Green and sustainable syntheses of biaryls

Handle URI:
http://hdl.handle.net/10754/575537
Title:
Suzuki-Miyaura cross-coupling reactions in aqueous media: Green and sustainable syntheses of biaryls
Authors:
Polshettiwar, Vivek ( 0000-0003-1375-9668 ) ; Decottignies, Audrey; Len, Christophe; Fihri, Aziz
Abstract:
Carbon-carbon cross-coupling reactions are among the most important processes in organic chemistry, and Suzuki-Miyaura reactions are among the most widely used protocols for the formation of carbon-carbon bonds. These reactions are generally catalyzed by soluble palladium complexes with various ligands. However, the use of toxic organic solvents remains a scientific challenge and an aspect of economical and ecological relevance. This Review will summarize various recently developed significant methods by which the Suzuki-Miyaura coupling was conducted in aqueous media, and analyzes if they are "real green" protocols. © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
KAUST Department:
KAUST Catalysis Center (KCC); Physical Sciences and Engineering (PSE) Division
Publisher:
Wiley-Blackwell
Journal:
ChemSusChem
Issue Date:
28-Feb-2010
DOI:
10.1002/cssc.200900221
PubMed ID:
20191633
Type:
Article
ISSN:
18645631
Sponsors:
We thank G. Santini for his support of this work and the Region Picardie for their financial support.
Appears in Collections:
Articles; Physical Sciences and Engineering (PSE) Division; KAUST Catalysis Center (KCC)

Full metadata record

DC FieldValue Language
dc.contributor.authorPolshettiwar, Viveken
dc.contributor.authorDecottignies, Audreyen
dc.contributor.authorLen, Christopheen
dc.contributor.authorFihri, Azizen
dc.date.accessioned2015-08-24T08:32:12Zen
dc.date.available2015-08-24T08:32:12Zen
dc.date.issued2010-02-28en
dc.identifier.issn18645631en
dc.identifier.pmid20191633en
dc.identifier.doi10.1002/cssc.200900221en
dc.identifier.urihttp://hdl.handle.net/10754/575537en
dc.description.abstractCarbon-carbon cross-coupling reactions are among the most important processes in organic chemistry, and Suzuki-Miyaura reactions are among the most widely used protocols for the formation of carbon-carbon bonds. These reactions are generally catalyzed by soluble palladium complexes with various ligands. However, the use of toxic organic solvents remains a scientific challenge and an aspect of economical and ecological relevance. This Review will summarize various recently developed significant methods by which the Suzuki-Miyaura coupling was conducted in aqueous media, and analyzes if they are "real green" protocols. © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.en
dc.description.sponsorshipWe thank G. Santini for his support of this work and the Region Picardie for their financial support.en
dc.publisherWiley-Blackwellen
dc.subjectCross couplingen
dc.subjectGreen chemistryen
dc.subjectMicrowave chemistryen
dc.subjectPalladiumen
dc.subjectSustainable chemistryen
dc.subjectWater chemistryen
dc.titleSuzuki-Miyaura cross-coupling reactions in aqueous media: Green and sustainable syntheses of biarylsen
dc.typeArticleen
dc.contributor.departmentKAUST Catalysis Center (KCC)en
dc.contributor.departmentPhysical Sciences and Engineering (PSE) Divisionen
dc.identifier.journalChemSusChemen
dc.contributor.institutionTransformations Intégrées de la Matière Renouvelable ESCOM-UTC, 1-Allée du Réseau, Jean-Marie Buckmaster, 60200 Compiègne, Franceen
kaust.authorPolshettiwar, Viveken

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