15844118

Source:http://linkedlifedata.com/resource/pubmed/id/15844118

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0127400, umls-concept:C0302917, umls-concept:C0449444, umls-concept:C0524535, umls-concept:C1140999, umls-concept:C1260969
pubmed:issue	21
pubmed:dateCreated	2005-5-26
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/GM65407
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0370543
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Cyclopentanes, http://linkedlifedata.com/resource/pubmed/chemical/Oxepins
pubmed:status	MEDLINE
pubmed:month	May
pubmed:issn	1433-7851
pubmed:author	pubmed-author:NasveschukChristopher GCG, pubmed-author:RovisTomislavT
pubmed:issnType	Print
pubmed:day	20
pubmed:volume	44
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	3264-7
pubmed:dateRevised	2007-11-14
pubmed:meshHeading	pubmed-meshheading:15844118-Cyclization, pubmed-meshheading:15844118-Cyclopentanes, pubmed-meshheading:15844118-Molecular Structure, pubmed-meshheading:15844118-Oxepins, pubmed-meshheading:15844118-Stereoisomerism
pubmed:year	2005
pubmed:articleTitle	Stereoselective Lewis acid mediated [1,3] ring contraction of 2,5-dihydrooxepins as a route to polysubstituted cyclopentenes.
pubmed:affiliation	Department of Chemistry, Colorado State University, Fort Collins, CO 80523, USA.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural