11720582

Source:http://linkedlifedata.com/resource/pubmed/id/11720582

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0441513, umls-concept:C0671542, umls-concept:C1527177, umls-concept:C1707877, umls-concept:C1883254, umls-concept:C2603343
pubmed:issue	24
pubmed:dateCreated	2001-11-26
pubmed:abstractText	In this, the second of two Letters, we describe an effective assembly of (+)-4, an eastern hemisphere subtarget comprising the FGH rings of (+)-nodulisporic acid A (1) (17 steps, 9% overall yield). Central to the synthesis is a Koga three-component conjugate addition-alkylation sequence which secures the trans orientation of the vicinal quaternary methyl groups. [reaction: see text]
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/GM-29028
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Indoles, http://linkedlifedata.com/resource/pubmed/chemical/nodulisporic acid A
pubmed:status	MEDLINE
pubmed:month	Nov
pubmed:issn	1523-7060
pubmed:author	pubmed-author:ChoY SYS, pubmed-author:IshiyamaHH, pubmed-author:SmithA BAB3rd
pubmed:issnType	Print
pubmed:day	29
pubmed:volume	3
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	3971-4
pubmed:dateRevised	2007-11-14
pubmed:meshHeading	pubmed-meshheading:11720582-Indoles, pubmed-meshheading:11720582-Molecular Structure
pubmed:year	2001
pubmed:articleTitle	Nodulisporic acid A synthetic studies. 2. Construction of an eastern hemisphere subtarget.
pubmed:affiliation	Department of Chemistry, University of Pennsylvania, Philadelphia, PA 19104, USA. smithab@sas.upenn.edu
pubmed:publicationType	Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't