12510291

Source:http://linkedlifedata.com/resource/pubmed/id/12510291

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0034760, umls-concept:C0205314, umls-concept:C0443286, umls-concept:C0679622, umls-concept:C1521827
pubmed:issue	22
pubmed:dateCreated	2003-1-3
pubmed:abstractText	Hitherto unknown, relatively labile gem-difluorinated vinyloxiranes were prepared by difluoro-Wittig reactions with alpha,beta-epoxyketones; for these vinyloxiranes alkyl groups were delivered at the fluorine-attached terminal carbon atom in an SN2' manner by RLi, while Me3Al and MeMgBr-CuCl (3: 1) introduced the Me group at the allylic epoxy carbon with retention and inversion of the original stereochemistry, respectively.
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:KitazumeTomoyaT, pubmed-author:UekiHisanoriH, pubmed-author:YamazakiTakashiT
pubmed:issnType	Print
pubmed:day	21
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	2670-1
pubmed:dateRevised	2003-11-4
pubmed:year	2002
pubmed:articleTitle	Preparation and regioselective reactions of novel gem-difluorinated vinyloxiranes with some organometallic reagents.
pubmed:affiliation	Graduate School of Bioscience and Bioengineering, Tokyo Institute of Technology, 4259 Nagatsuta-cho, Midori-ku, Yokohama 226-8501, Japan.
pubmed:publicationType	Journal Article