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Clean and fast cross-coupling of aryl halides in one-pot

Academic Article
Publication Date:
2014
abstract:
Unsymmetrically coupled biaryls are synthesized in high yield starting from different aryl bromides and bis(pinacolato)diboron by carrying out the Miyaura borylation reaction followed by the Suzuki-Miyaura reaction in the same reaction pot over 1-2 mol % SiliaCat DPP-Pd. The SiliaCat DPP-Pd catalyst is air-stable and the method does not require the use of inert conditions. The use of non-toxic isopropanol or 2-butanol as reaction solvent further adds to the environmental benefits of this new green synthetic methodology. © 2014 Pandarus et al; licensee Beilstein-Institut.
Iris type:
01.01 Articolo in rivista
Keywords:
Borylation; Cross-coupling; One-pot; SiliaCat; Suzuki-Miyaura
List of contributors:
Ciriminna, Rosaria; Pagliaro, Mario
Authors of the University:
CIRIMINNA ROSARIA
PAGLIARO MARIO
Handle:
https://iris.cnr.it/handle/20.500.14243/256890
Published in:
BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY
Journal
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http://www.scopus.com/record/display.url?eid=2-s2.0-84899759324&origin=inward
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