21520374

Source:http://linkedlifedata.com/resource/pubmed/id/21520374

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0007382, umls-concept:C0175892, umls-concept:C0205250, umls-concept:C0220781, umls-concept:C1704788, umls-concept:C1883254
pubmed:issue	22
pubmed:dateCreated	2011-5-16
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/GM-068649
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0370543
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Palladium, http://linkedlifedata.com/resource/pubmed/chemical/Peptides, http://linkedlifedata.com/resource/pubmed/chemical/Terphenyl Compounds
pubmed:status	MEDLINE
pubmed:month	May
pubmed:issn	1521-3773
pubmed:author	pubmed-author:BarrettKimberly TKT, pubmed-author:GustafsonJeffrey LJL, pubmed-author:LimDanielD, pubmed-author:MillerScott JSJ
pubmed:issnType	Electronic
pubmed:day	23
pubmed:volume	50
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	5125-9
pubmed:meshHeading	pubmed-meshheading:21520374-Catalysis, pubmed-meshheading:21520374-Halogenation, pubmed-meshheading:21520374-Palladium, pubmed-meshheading:21520374-Peptides, pubmed-meshheading:21520374-Stereoisomerism, pubmed-meshheading:21520374-Terphenyl Compounds
pubmed:year	2011
pubmed:articleTitle	Synthesis of atropisomerically defined, highly substituted biaryl scaffolds through catalytic enantioselective bromination and regioselective cross-coupling.
pubmed:affiliation	Department of Chemistry, Yale University, New Haven, CT 06520-8107, USA.
pubmed:publicationType	Journal Article, Research Support, N.I.H., Extramural