20384311

Source:http://linkedlifedata.com/resource/pubmed/id/20384311

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Predicate	Object
rdf:type	pubmed:Citation
pubmed:issue	9
pubmed:dateCreated	2010-4-30
pubmed:abstractText	Systematically designed oxazolidinone-derived enecarbamates reveal that solvent and temperature effects on the stereoselectivity during photooxygenation are likely due to the conformational flexibility of the chiral phenethyl side chain (entropy factors); the extent of enantiomeric excess in the photoproduct is dictated by the alkene geometry.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:status	PubMed-not-MEDLINE
pubmed:month	May
pubmed:issn	1523-7052
pubmed:author	pubmed-author:AdamWaldemarW, pubmed-author:JockuschSteffenS, pubmed-author:SivaguruJJ, pubmed-author:SolomonMarissa RMR, pubmed-author:TurroNicholas JNJ
pubmed:issnType	Electronic
pubmed:day	7
pubmed:volume	12
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	2142-5
pubmed:year	2010
pubmed:articleTitle	Decoding stereocontrol during the photooxygenation of oxazolidinone-functionalized enecarbamates.
pubmed:affiliation	Department of Chemistry, Columbia University, 3000 Broadway, New York, New York 10027, USA.
pubmed:publicationType	Journal Article