11430021

Source:http://linkedlifedata.com/resource/pubmed/id/11430021

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0002074, umls-concept:C0022634, umls-concept:C0023688, umls-concept:C0205250, umls-concept:C0332514, umls-concept:C0596514
pubmed:issue	2
pubmed:dateCreated	2001-6-29
pubmed:abstractText	[figure: see text] Ferrocene-modified chiral pocket ligands have been studied in the palladium-catalyzed asymmetric alkylation of simple ketone enolates, in which (R,R,Sp,Sp)-1 containing two pairs of matched chiralities, central chirality and planar chirality, behaved very efficiently in this reaction and up to 95% ee value was achieved.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Jan
pubmed:issn	1523-7060
pubmed:author	pubmed-author:GohW SWS, pubmed-author:LawD FDF, pubmed-author:YouS LSL, pubmed-author:ZhuX ZXZ
pubmed:issnType	Print
pubmed:day	25
pubmed:volume	3
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	149-51
pubmed:dateRevised	2003-10-31
pubmed:year	2001
pubmed:articleTitle	Highly efficient ligands for palladium-catalyzed asymmetric alkylation of ketone enolates.
pubmed:affiliation	Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032, China.
pubmed:publicationType	Journal Article