11429911

Source:http://linkedlifedata.com/resource/pubmed/id/11429911

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0028131, umls-concept:C0030015, umls-concept:C0598128
pubmed:issue	1
pubmed:dateCreated	2001-6-29
pubmed:abstractText	Efficient routes to the synthesis of norbornadiene-tethered nitrile oxides have been developed, and their intramolecular 1,3-dipolar cycloadditions were studied. The cycloadditions occurred in good yields for a variety of substrates and were found to be highly regio- and stereoselective, giving single regio- and stereoisomers in most cases.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985193R
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Jan
pubmed:issn	0022-3263
pubmed:author	pubmed-author:HandersonSS, pubmed-author:TamWW, pubmed-author:TranmerG KGK, pubmed-author:YipCC
pubmed:issnType	Print
pubmed:day	12
pubmed:volume	66
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	276-86
pubmed:dateRevised	2003-10-31
pubmed:year	2001
pubmed:articleTitle	Intramolecular 1,3-dipolar cycloadditions of norbornadiene-tethered nitrile oxides.
pubmed:affiliation	Guelph-Waterloo Centre for Graduate Work in Chemistry and Biochemistry, Department of Chemistry and Biochemistry, University of Guelph, Guelph, Ontario, Canada N1G 2W1.
pubmed:publicationType	Journal Article