11178816

Source:http://linkedlifedata.com/resource/pubmed/id/11178816

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0220781, umls-concept:C1883254
pubmed:issue	4
pubmed:dateCreated	2001-2-22
pubmed:abstractText	[reaction: see text] Enantioselective synthesis of attenols A and B was accomplished by using diastereoselective hydroboration, Lindlar reduction, and acid-catalyzed acetal formation.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Ethers, Cyclic
pubmed:status	MEDLINE
pubmed:month	Feb
pubmed:issn	1523-7060
pubmed:author	pubmed-author:ArakiKK, pubmed-author:SengokuTT, pubmed-author:SuenagaKK, pubmed-author:UemuraDD
pubmed:issnType	Print
pubmed:day	22
pubmed:volume	3
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	527-9
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:11178816-Animals, pubmed-meshheading:11178816-Bivalvia, pubmed-meshheading:11178816-Ethers, Cyclic, pubmed-meshheading:11178816-Molecular Conformation, pubmed-meshheading:11178816-Molecular Structure, pubmed-meshheading:11178816-Stereoisomerism, pubmed-meshheading:11178816-Structure-Activity Relationship
pubmed:year	2001
pubmed:articleTitle	Enantioselective synthesis of attenols A and B.
pubmed:affiliation	Department of Chemistry, Graduate School of Science, Nagoya University, Chikusa, Nagoya 464-8602, Japan. uemura@chem3.chem.nagoya-u.ac.jp
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't