19278207

Source:http://linkedlifedata.com/resource/pubmed/id/19278207

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0022634, umls-concept:C1142790
pubmed:issue	8
pubmed:dateCreated	2009-4-9
pubmed:abstractText	Aryl cyclopropyl ketones undergo nickel-catalyzed borylative ring opening with bis(pinacolato)diboron to yield 4-oxoalkylboronates.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985193R
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Apr
pubmed:issn	1520-6904
pubmed:author	pubmed-author:OshimaKoichiroK, pubmed-author:SumidaYutoY, pubmed-author:YorimitsuHidekiH
pubmed:issnType	Electronic
pubmed:day	17
pubmed:volume	74
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	3196-8
pubmed:year	2009
pubmed:articleTitle	Nickel-catalyzed borylation of aryl cyclopropyl ketones with bis(pinacolato)diboron to synthesize 4-oxoalkylboronates.
pubmed:affiliation	Department of Material Chemistry, Graduate School of Engineering, Kyoto University, Kyoto-daigaku Katsura, Nishikyo-ku, Kyoto 615-8510, Japan.
pubmed:publicationType	Journal Article