20000440

Source:http://linkedlifedata.com/resource/pubmed/id/20000440

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0037968, umls-concept:C0075804, umls-concept:C0220781, umls-concept:C0443286, umls-concept:C1511695, umls-concept:C1883254, umls-concept:C2936395
pubmed:issue	2
pubmed:dateCreated	2010-1-11
pubmed:abstractText	A highly efficient oxidative coupling of 2-naphthols and a rearrangement tandem reaction to afford unique spiro compounds in the presence of FeCl(3).6H(2)O in up to 88% yield have been developed.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/2-naphthol, http://linkedlifedata.com/resource/pubmed/chemical/Naphthols, http://linkedlifedata.com/resource/pubmed/chemical/Spiro Compounds
pubmed:status	MEDLINE
pubmed:month	Jan
pubmed:issn	1523-7052
pubmed:author	pubmed-author:KawabataTakeoT, pubmed-author:SasamoriTakahiroT, pubmed-author:SueDaisukeD, pubmed-author:TokitohNobuhiroN, pubmed-author:TsubakiKazunoriK
pubmed:issnType	Electronic
pubmed:day	15
pubmed:volume	12
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	256-8
pubmed:meshHeading	pubmed-meshheading:20000440-Crystallography, X-Ray, pubmed-meshheading:20000440-Models, Molecular, pubmed-meshheading:20000440-Molecular Structure, pubmed-meshheading:20000440-Naphthols, pubmed-meshheading:20000440-Oxidation-Reduction, pubmed-meshheading:20000440-Spiro Compounds, pubmed-meshheading:20000440-Stereoisomerism
pubmed:year	2010
pubmed:articleTitle	Synthesis of spiro compounds through tandem oxidative coupling and a framework rearrangement reaction.
pubmed:affiliation	Institute for Chemical Research, Kyoto University, Uji, Kyoto, 611-0011, Japan.
pubmed:publicationType	Journal Article