15053588

Source:http://linkedlifedata.com/resource/pubmed/id/15053588

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0020930, umls-concept:C0031679, umls-concept:C0444454
pubmed:issue	13
pubmed:dateCreated	2004-3-31
pubmed:abstractText	Chiral thiourea 1b catalyzes the highly enantioselective hydrophosphonylation of a wide range of N-benzyl imines. The hydrophosphonylation products are readily deprotected by hydrogenolysis, providing access to free alpha-amino phosphonic acids in highly enantioenriched form.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7503056
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Apr
pubmed:issn	0002-7863
pubmed:author	pubmed-author:JacobsenEric NEN, pubmed-author:JolyGuy DGD
pubmed:issnType	Print
pubmed:day	7
pubmed:volume	126
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	4102-3
pubmed:dateRevised	2008-1-17
pubmed:year	2004
pubmed:articleTitle	Thiourea-catalyzed enantioselective hydrophosphonylation of imines: practical access to enantiomerically enriched alpha-amino phosphonic acids.
pubmed:affiliation	Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts, USA.
pubmed:publicationType	Journal Article