19370881

Source:http://linkedlifedata.com/resource/pubmed/id/19370881

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0220781, umls-concept:C0311404, umls-concept:C0376525, umls-concept:C1883254, umls-concept:C2716378, umls-concept:C2716379
pubmed:issue	1
pubmed:dateCreated	2009-4-17
pubmed:abstractText	The synthesis of two natural products, the para-para dimer of 8-methoxynaphthalen-1-ol (2), daldinol (3), and the related ortho-para dimer nodulisporin A (4) was achieved by the oxidation of 2 with ammonium metapervanadate (NH4VO3).
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/101477873
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Naphthalenes
pubmed:status	MEDLINE
pubmed:month	Jan
pubmed:issn	1934-578X
pubmed:author	pubmed-author:AslanAbdulselamA, pubmed-author:KrohnKarstenK
pubmed:issnType	Print
pubmed:volume	4
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	87-8
pubmed:meshHeading	pubmed-meshheading:19370881-Ascomycota, pubmed-meshheading:19370881-Molecular Structure, pubmed-meshheading:19370881-Naphthalenes
pubmed:year	2009
pubmed:articleTitle	Synthesis of daldinol and nodulisporin A by oxidative dimerization of 8-methoxynaphthalen-1-ol.
pubmed:affiliation	Department of Chemistry, University of Paderborn, Warburger Str. 100, 33098 Paderborn, Germany. k.krohn@uni-paderborn.de
pubmed:publicationType	Journal Article