12465926

Source:http://linkedlifedata.com/resource/pubmed/id/12465926

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0220781, umls-concept:C0439810, umls-concept:C1173916, umls-concept:C1883254
pubmed:issue	25
pubmed:dateCreated	2002-12-5
pubmed:abstractText	[reaction: see text] The stereocontrolled total synthesis of (-)-O-methylpallidinine, a naturally occurring Morphinan alkaloid with a B/C-trans-hydrophenanthrene framework, has been achieved starting from the chiral bicyclo[3.2.1]octenone building block by employing a single-step dihydrophenanthrene formation reaction as the key step.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Bridged Compounds, http://linkedlifedata.com/resource/pubmed/chemical/Morphinans
pubmed:status	MEDLINE
pubmed:month	Dec
pubmed:issn	1523-7060
pubmed:author	pubmed-author:HanadaKeisukeK, pubmed-author:MiyazawaNorioN, pubmed-author:OgasawaraKunioK
pubmed:issnType	Print
pubmed:day	12
pubmed:volume	4
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	4515-7
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:12465926-Bridged Compounds, pubmed-meshheading:12465926-Molecular Conformation, pubmed-meshheading:12465926-Molecular Structure, pubmed-meshheading:12465926-Morphinans, pubmed-meshheading:12465926-Plants
pubmed:year	2002
pubmed:articleTitle	The stereocontrolled total synthesis of (-)-O-methylpallidinine.
pubmed:affiliation	Pharmaceutical Institute, Tohoku University, Aobayama, Sendai 980-8578, Japan.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't