10825955

Source:http://linkedlifedata.com/resource/pubmed/id/10825955

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0220781, umls-concept:C0443286, umls-concept:C1883254
pubmed:issue	7
pubmed:dateCreated	2000-6-20
pubmed:abstractText	[formula: see text] A convenient regio- and stereoselective preparation of 1,2,5,6-tetrahydropyridines of the type 1 has been developed, starting from readily available N-acyl-2,3-dihydro-4-pyridones 2.
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/GM 34442
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Pyridines, http://linkedlifedata.com/resource/pubmed/chemical/Pyridones
pubmed:status	MEDLINE
pubmed:month	Oct
pubmed:issn	1523-7060
pubmed:author	pubmed-author:CominsD LDL, pubmed-author:KuetheJ TJT
pubmed:issnType	Print
pubmed:day	7
pubmed:volume	1
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1031-3
pubmed:dateRevised	2007-11-14
pubmed:meshHeading	pubmed-meshheading:10825955-Pyridines, pubmed-meshheading:10825955-Pyridones, pubmed-meshheading:10825955-Stereoisomerism
pubmed:year	1999
pubmed:articleTitle	The Mukaiyama-Michael reaction of N-acyl-2,3-dihydro-4-pyridones: regio- and stereoselective synthesis of cis-2,6-disubstituted 1,2,5,6-tetrahydropyridines.
pubmed:affiliation	Department of Chemistry, North Carolina State University, Raleigh 27695-8204, USA.
pubmed:publicationType	Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, U.S. Gov't, Non-P.H.S., Research Support, Non-U.S. Gov't