16268525

Source:http://linkedlifedata.com/resource/pubmed/id/16268525

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0002074, umls-concept:C0002505, umls-concept:C0014898, umls-concept:C0023688, umls-concept:C0205250
pubmed:issue	23
pubmed:dateCreated	2005-11-4
pubmed:abstractText	[reaction, structure: see text] Pd-catalyzed asymmetric allylic alkylation of dienyl acetates 1 and amination of allyl acetates 2 provides the corresponding chiral products in high regio- and enantioselectivities using 1,1'-P,N-ferrocenes L1a and L2d as ligands, respectively.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Nov
pubmed:issn	1523-7060
pubmed:author	pubmed-author:HouXue-LongXL, pubmed-author:SunNaN, pubmed-author:ZhengWen-HuaWH
pubmed:issnType	Print
pubmed:day	10
pubmed:volume	7
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	5151-4
pubmed:year	2005
pubmed:articleTitle	Highly regio- and enantioselective palladium-catalyzed allylic alkylation and amination of dienyl esters with 1,1'-P,N-ferrocene ligands.
pubmed:affiliation	State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Road, Shanghai 200032, China.
pubmed:publicationType	Journal Article