19924879

Source:http://linkedlifedata.com/resource/pubmed/id/19924879

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0021243, umls-concept:C0205250, umls-concept:C0596311, umls-concept:C1330957, umls-concept:C2936395
pubmed:issue	24
pubmed:dateCreated	2009-12-16
pubmed:abstractText	A highly regioselective oxidative coupling reaction between indolizines and vinylarenes has been accomplished in the presence of palladium catalysts to give only the branched alpha-product in high efficiency. The regioselectivity is promoted significantly by bidentate nitrogen ligands.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Dec
pubmed:issn	1523-7052
pubmed:author	pubmed-author:ChengKaiK, pubmed-author:YangYuzhuY, pubmed-author:ZhangYuhongY
pubmed:issnType	Electronic
pubmed:day	17
pubmed:volume	11
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	5606-9
pubmed:year	2009
pubmed:articleTitle	Highly regioselective palladium-catalyzed oxidative coupling of indolizines and vinylarenes via C-H bond cleavage.
pubmed:affiliation	Department of Chemistry, Zhejiang University, Hangzhou 310027, People's Republic of China.
pubmed:publicationType	Journal Article