17057865

Source:http://linkedlifedata.com/resource/pubmed/id/17057865

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0010546, umls-concept:C0022634, umls-concept:C0030020, umls-concept:C0220781, umls-concept:C1883254
pubmed:issue	42
pubmed:dateCreated	2006-10-23
pubmed:abstractText	2-(Trifluoromethyl)allyl ketone O-pentafluorobenzoyloximes undergo a palladium-catalyzed 5-endo mode of alkene insertion via oxidative addition of the N-O bond, followed by beta-fluorine elimination to produce 4-difluoromethylene-1-pyrrolines.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9610838
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Nov
pubmed:issn	1359-7345
pubmed:author	pubmed-author:IchikawaJunjiJ, pubmed-author:ItoNaotakaN, pubmed-author:NadanoRyoR
pubmed:issnType	Print
pubmed:day	13
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	4425-7
pubmed:year	2006
pubmed:articleTitle	5-endo Heck-type cyclization of 2-(trifluoromethyl)allyl ketone oximes: Synthesis of 4-difluoromethylene-substituted 1-pyrrolines.
pubmed:affiliation	Department of Chemistry, Graduate School of Science, The University of Tokyo, Bunkyo-ku, Tokyo, Japan. junji@chem.s.u-tokyo.ac.jp
pubmed:publicationType	Journal Article