16928047

Source:http://linkedlifedata.com/resource/pubmed/id/16928047

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0025664, umls-concept:C0031960, umls-concept:C0998924
pubmed:issue	18
pubmed:dateCreated	2006-8-24
pubmed:abstractText	1,2,3,4-Tetrahydropyridines were halogenated upon treatment with iodine to obtain the desired cross-coupling precursors. Diastereoselective hydrogenation of Suzuki cross-coupling adducts allowed the facile asymmetric synthesis of 2,5-cis-substituted piperidines in five steps from readily available pyridine.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Aug
pubmed:issn	1523-7060
pubmed:author	pubmed-author:CharetteAndré BAB, pubmed-author:LarivéeAlexandreA
pubmed:issnType	Print
pubmed:day	31
pubmed:volume	8
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	3955-7
pubmed:year	2006
pubmed:articleTitle	New methodology toward chiral, non-racemic 2,5-cis-substituted piperidines via Suzuki cross-coupling.
pubmed:affiliation	Département de Chimie, Université de Montréal, P.O. Box 6128, Station Downtown, Montréal, Québec, Canada H3C 3J7.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't