14680232

Source:http://linkedlifedata.com/resource/pubmed/id/14680232

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0348080, umls-concept:C0443286, umls-concept:C2700116
pubmed:issue	23
pubmed:dateCreated	2003-12-18
pubmed:abstractText	N-Allylic difluoroenamines exhibited unusual behaviors under thermal conditions; N-allyl difluoroenamines in refluxing xylene afforded not only aza-Claisen rearrangement products, but also 2-azabicyclo[2.1.1]hexanes, whose formation could be explained via intramolecular [2+2]-cycloaddition, whilst N-prenyl difluoroenamine underwent an ene reaction to give the pyrrolidine as a sole product.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9610838
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Dec
pubmed:issn	1359-7345
pubmed:author	pubmed-author:AmiiHidekiH, pubmed-author:IchiharaYutakaY, pubmed-author:KobayashiTakeshiT, pubmed-author:NakagawaTakashiT, pubmed-author:UneyamaKenjiK
pubmed:issnType	Print
pubmed:day	7
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	2902-3
pubmed:year	2003
pubmed:articleTitle	Unusual reactions of N-allylic difluoroenamines under thermal conditions.
pubmed:affiliation	Department of Applied Chemistry, Faculty of Engineering, Okayama University, Okayama 700-8530, Japan.
pubmed:publicationType	Journal Article