Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
19
pubmed:dateCreated
2006-9-8
pubmed:abstractText
meso-2,4-Bis(diphenylphosphino)pentane (mBDPP) has proved to be an effective regiocontrolling ligand for palladium-catalyzed internal arylation by aryl bromides of electron-rich olefins in a common solvent DMSO with no need for any halide scavengers. The arylation of the benchmark electron-rich olefin butyl vinyl ether took place smoothly to afford exclusively alpha-arylated product with high isolated yields. The better performance of mBDPP, compared with that of the commonly used DPPP [1,3-bis(diphenylphosphino)propane], highlights the important but subtle effect of ligand on the regioselectivity of the Heck arylation reactions.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/2,4-bis(diphenylphosphino)pentane, http://linkedlifedata.com/resource/pubmed/chemical/Alkenes, http://linkedlifedata.com/resource/pubmed/chemical/Ethers, http://linkedlifedata.com/resource/pubmed/chemical/Hydrocarbons, Brominated, http://linkedlifedata.com/resource/pubmed/chemical/Hydrocarbons, Halogenated, http://linkedlifedata.com/resource/pubmed/chemical/Naphthalenes, http://linkedlifedata.com/resource/pubmed/chemical/Palladium, http://linkedlifedata.com/resource/pubmed/chemical/Pentanes, http://linkedlifedata.com/resource/pubmed/chemical/Phosphines, http://linkedlifedata.com/resource/pubmed/chemical/Vinyl Compounds, http://linkedlifedata.com/resource/pubmed/chemical/n-butyl vinyl ether, http://linkedlifedata.com/resource/pubmed/chemical/naphthalene
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
0022-3263
pubmed:author
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
71
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
7467-70
pubmed:meshHeading
pubmed:year
2006
pubmed:articleTitle
Pd-mBDPP-catalyzed regioselective internal arylation of electron-rich olefins by aryl halides.
pubmed:affiliation
Department of Chemistry, Liverpool Centre for Materials and Catalysis, University of Liverpool, Liverpool L697ZD, UK.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't