11428007

Source:http://linkedlifedata.com/resource/pubmed/id/11428007

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Subject	Predicate	Object	Context
pubmed-article:11428007	rdf:type	pubmed:Citation	lld:pubmed
pubmed-article:11428007	lifeskim:mentions	umls-concept:C1708096	lld:lifeskim
pubmed-article:11428007	lifeskim:mentions	umls-concept:C0220781	lld:lifeskim
pubmed-article:11428007	lifeskim:mentions	umls-concept:C1883254	lld:lifeskim
pubmed-article:11428007	lifeskim:mentions	umls-concept:C0768793	lld:lifeskim
pubmed-article:11428007	pubmed:issue	3	lld:pubmed
pubmed-article:11428007	pubmed:dateCreated	2001-6-28	lld:pubmed
pubmed-article:11428007	pubmed:abstractText	[figure: see text] The use of several non-aldol aldol processes allows one to prepare a fully functionalized and completely protected C1-C11 fragment that should be useful for the total synthesis of the tedanolides.	lld:pubmed
pubmed-article:11428007	pubmed:grant	http://linkedlifedata.com/r...	lld:pubmed
pubmed-article:11428007	pubmed:language	eng	lld:pubmed
pubmed-article:11428007	pubmed:journal	http://linkedlifedata.com/r...	lld:pubmed
pubmed-article:11428007	pubmed:citationSubset	IM	lld:pubmed
pubmed-article:11428007	pubmed:chemical	http://linkedlifedata.com/r...	lld:pubmed
pubmed-article:11428007	pubmed:chemical	http://linkedlifedata.com/r...	lld:pubmed
pubmed-article:11428007	pubmed:chemical	http://linkedlifedata.com/r...	lld:pubmed
pubmed-article:11428007	pubmed:chemical	http://linkedlifedata.com/r...	lld:pubmed
pubmed-article:11428007	pubmed:status	MEDLINE	lld:pubmed
pubmed-article:11428007	pubmed:month	Feb	lld:pubmed
pubmed-article:11428007	pubmed:issn	1523-7060	lld:pubmed
pubmed-article:11428007	pubmed:author	pubmed-author:LeeC PCP	lld:pubmed
pubmed-article:11428007	pubmed:author	pubmed-author:JungM EME	lld:pubmed
pubmed-article:11428007	pubmed:issnType	Print	lld:pubmed
pubmed-article:11428007	pubmed:day	8	lld:pubmed
pubmed-article:11428007	pubmed:volume	3	lld:pubmed
pubmed-article:11428007	pubmed:owner	NLM	lld:pubmed
pubmed-article:11428007	pubmed:authorsComplete	Y	lld:pubmed
pubmed-article:11428007	pubmed:pagination	333-6	lld:pubmed
pubmed-article:11428007	pubmed:dateRevised	2008-11-21	lld:pubmed
pubmed-article:11428007	pubmed:meshHeading	pubmed-meshheading:11428007...	lld:pubmed
pubmed-article:11428007	pubmed:meshHeading	pubmed-meshheading:11428007...	lld:pubmed
pubmed-article:11428007	pubmed:meshHeading	pubmed-meshheading:11428007...	lld:pubmed
pubmed-article:11428007	pubmed:meshHeading	pubmed-meshheading:11428007...	lld:pubmed
pubmed-article:11428007	pubmed:meshHeading	pubmed-meshheading:11428007...	lld:pubmed
pubmed-article:11428007	pubmed:year	2001	lld:pubmed
pubmed-article:11428007	pubmed:articleTitle	Synthesis of a fully functionalized protected C1-C11 fragment for the synthesis of the tedanolides.	lld:pubmed
pubmed-article:11428007	pubmed:affiliation	Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095-1569, USA. jung@chem.ucla.edu	lld:pubmed
pubmed-article:11428007	pubmed:publicationType	Journal Article	lld:pubmed
pubmed-article:11428007	pubmed:publicationType	Research Support, U.S. Gov't, P.H.S.	lld:pubmed
http://linkedlifedata.com/r...	pubmed:referesTo	pubmed-article:11428007	lld:pubmed
http://linkedlifedata.com/r...	pubmed:referesTo	pubmed-article:11428007	lld:pubmed