15997285

Source:http://linkedlifedata.com/resource/pubmed/id/15997285

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0205174, umls-concept:C0439851, umls-concept:C1522449, umls-concept:C1552596, umls-concept:C1947931
pubmed:issue	27
pubmed:dateCreated	2005-7-5
pubmed:abstractText	Oxazolidinone-functionalized enecarbamates undergo diastereoselective E/Z photoisomerization upon direct and triplet sensitized irradiations with chiral/achiral sensitizers, showing that the enhanced product diastereoselectivity depends on the solvent and temperature.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9610838
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Jul
pubmed:issn	1359-7345
pubmed:author	pubmed-author:AdamWaldemarW, pubmed-author:InoueYoshihisaY, pubmed-author:JockuschSteffenS, pubmed-author:SaitoHideakiH, pubmed-author:SivaguruJJ, pubmed-author:TurroNicholas JNJ
pubmed:issnType	Print
pubmed:day	21
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	3424-6
pubmed:year	2005
pubmed:articleTitle	Stereoselective E/Z photoisomerization of oxazolidinone functionalized enecarbamates: direct and triplet sensitized irradiation.
pubmed:affiliation	Department of Chemistry and the Department of Chemical Engineering, Columbia University, 3000 Broadway, Mail Code 3119, New York, NY 10027, USA.
pubmed:publicationType	Journal Article