20540067

Source:http://linkedlifedata.com/resource/pubmed/id/20540067

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0002068, umls-concept:C0443286, umls-concept:C1521827, umls-concept:C1704419
pubmed:issue	8
pubmed:dateCreated	2010-8-4
pubmed:abstractText	Treatment of trifluorovinyl- or pentafluoropropen-1-yl sulfone or sulfoxide, which are easily prepared from commercially available 1,2-dibromofluoroalkanes, with various organocuprates affords substitution or beta-reduction products in good to excellent yields through an addition-elimination reaction sequence.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/101294643
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Aug
pubmed:issn	1861-471X
pubmed:author	pubmed-author:IshiharaTakashiT, pubmed-author:KonnoTsutomuT, pubmed-author:ShimojiKanokoK, pubmed-author:TakahashiToshioT, pubmed-author:YamadaShigeyukiS
pubmed:issnType	Electronic
pubmed:day	2
pubmed:volume	5
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1846-53
pubmed:year	2010
pubmed:articleTitle	An effective preparation of sulfonyl- or sulfinyl-substituted fluorinated alkenes and their stereoselective addition-elimination reactions with organocuprates.
pubmed:affiliation	Department of Chemistry and Materials Technology, Kyoto Institute of Technology, Matsugasaki, Sakyo-ku, Kyoto 606-8585, Japan.
pubmed:publicationType	Journal Article