http://www.cnr.it/ontology/cnr/individuo/prodotto/ID283422
Clean and fast cross-coupling of aryl halides in one-pot (Articolo in rivista)
- Type
- Label
- Clean and fast cross-coupling of aryl halides in one-pot (Articolo in rivista) (literal)
- Anno
- 2014-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.3762/bjoc.10.87 (literal)
- Alternative label
Pandarus, Valerica; Gingras, Geneviéve; Béland, François; Ciriminna, R.; Pagliaro, Mario (2014)
Clean and fast cross-coupling of aryl halides in one-pot
in Beilstein journal of organic chemistry
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Pandarus, Valerica; Gingras, Geneviéve; Béland, François; Ciriminna, R.; Pagliaro, Mario (literal)
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
- http://www.scopus.com/record/display.url?eid=2-s2.0-84899759324&origin=inward (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Note
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- SiliCycle Inc.; Istituto Per Lo Studio Dei Materiali Nanostrutturati, Rome (literal)
- Titolo
- Clean and fast cross-coupling of aryl halides in one-pot (literal)
- 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. (literal)
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