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pubmed-article:17057865pubmed:dateCreated2006-10-23lld:pubmed
pubmed-article:17057865pubmed:abstractText2-(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.lld:pubmed
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pubmed-article:17057865pubmed:authorpubmed-author:IchikawaJunji...lld:pubmed
pubmed-article:17057865pubmed:authorpubmed-author:NadanoRyoRlld:pubmed
pubmed-article:17057865pubmed:authorpubmed-author:ItoNaotakaNlld:pubmed
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pubmed-article:17057865pubmed:pagination4425-7lld:pubmed
pubmed-article:17057865pubmed:year2006lld:pubmed
pubmed-article:17057865pubmed:articleTitle5-endo Heck-type cyclization of 2-(trifluoromethyl)allyl ketone oximes: Synthesis of 4-difluoromethylene-substituted 1-pyrrolines.lld:pubmed
pubmed-article:17057865pubmed:affiliationDepartment of Chemistry, Graduate School of Science, The University of Tokyo, Bunkyo-ku, Tokyo, Japan. junji@chem.s.u-tokyo.ac.jplld:pubmed
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