18480904

Source:http://linkedlifedata.com/resource/pubmed/id/18480904

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0243071, umls-concept:C1957670
pubmed:issue	11
pubmed:dateCreated	2008-5-15
pubmed:abstractText	Some nonenzymic epoxide-initiated polyolefin cyclization are reported. The presented molecules are partially constrained analogues of (3S)-oxidosqualene, the natural substrate to many important cyclase enzymes. These model compounds feature a preformed C-ring with built-in stereochemical information. The experimental results allow for an instructive comparison with the enzymic processes, particularly those of the cyclases in steroid biosynthesis (i.e. lanosterol synthase).
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/101154995
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Squalene, http://linkedlifedata.com/resource/pubmed/chemical/oxidosqualene
pubmed:status	MEDLINE
pubmed:month	Jun
pubmed:issn	1477-0520
pubmed:author	pubmed-author:De ClercqPierre JPJ, pubmed-author:MilanesioMarcoM, pubmed-author:PattisonPhilipP, pubmed-author:ViterboDavideD, pubmed-author:WinneJohan MJM
pubmed:issnType	Print
pubmed:day	7
pubmed:volume	6
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1918-25
pubmed:meshHeading	pubmed-meshheading:18480904-Cyclization, pubmed-meshheading:18480904-Models, Molecular, pubmed-meshheading:18480904-Molecular Conformation, pubmed-meshheading:18480904-Squalene
pubmed:year	2008
pubmed:articleTitle	Nonenzymic polycyclization of analogues of oxidosqualene with a preformed C-ring.
pubmed:affiliation	Ghent University, Department of Organic Chemistry, Krijgslaan 281 (S4), B-9000 Gent, Belgium.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't