15524450

Source:http://linkedlifedata.com/resource/pubmed/id/15524450

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0443286, umls-concept:C2587213
pubmed:issue	23
pubmed:dateCreated	2004-11-4
pubmed:abstractText	A catalytic asymmetric Passerini reaction using tridentate indan (pybox) Cu(II) Lewis acid complex 4 with substrates capable of bidentate coordination has been achieved. The reaction occurs via ligand-accelerated catalysis.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Indans, http://linkedlifedata.com/resource/pubmed/chemical/indan
pubmed:status	MEDLINE
pubmed:month	Nov
pubmed:issn	1523-7060
pubmed:author	pubmed-author:AndreanaPeter RPR, pubmed-author:LiuChang CCC, pubmed-author:SchreiberStuart LSL
pubmed:issnType	Print
pubmed:day	11
pubmed:volume	6
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	4231-3
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:15524450-Catalysis, pubmed-meshheading:15524450-Indans, pubmed-meshheading:15524450-Stereoisomerism
pubmed:year	2004
pubmed:articleTitle	Stereochemical control of the Passerini reaction.
pubmed:affiliation	Howard Hughes Medical Institute, Center for Chemical Methodology and Library Development (CMLD-HU) & Broad Institute of Harvard and MIT, Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts 02138, USA.
pubmed:publicationType	Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't