12109094

Source:http://linkedlifedata.com/resource/pubmed/id/12109094

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0001128, umls-concept:C0016330, umls-concept:C0205345, umls-concept:C0205360, umls-concept:C0684224, umls-concept:C1280500
pubmed:issue	11
pubmed:dateCreated	2002-7-11
pubmed:abstractText	(+/-)-Erythro- and (+/-)-threo-9,10-difluorostearic acids, which differ only by a stereogenic interconversion of a single C-F bond, have significantly different conformational stabilities.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9610838
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Jun
pubmed:issn	1359-7345
pubmed:author	pubmed-author:O'HaganDavidD, pubmed-author:PearsonChristopherC, pubmed-author:PettyMichael CMC, pubmed-author:TavasliMustafaM
pubmed:issnType	Print
pubmed:day	7
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1226-7
pubmed:dateRevised	2003-11-3
pubmed:year	2002
pubmed:articleTitle	The fluorine gauche effect. Langmuir isotherms report the relative conformational stability of (+/-)-erythro- and (+/-)-threo-9,10-difluorostearic acids.
pubmed:affiliation	School of Chemistry, University of St Andrews, Centre for Biomolecular Sciences, Haugh, North St Andrews, Fife, UK KY16 9ST.
pubmed:publicationType	Journal Article