19254002

Source:http://linkedlifedata.com/resource/pubmed/id/19254002

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0220781, umls-concept:C1511695, umls-concept:C1883254
pubmed:issue	7
pubmed:dateCreated	2009-3-26
pubmed:abstractText	Chiral allenamides are prepared with high levels of enantiomeric purity by [2,3]-sigmatropic rearrangement of propargylic sulfimides. The required branched propargylic sulfides are prepared by an enantioselective organocatalytic aldehyde alpha-sulfenylation followed by Corey-Fuchs alkynylation.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Aldehydes, http://linkedlifedata.com/resource/pubmed/chemical/Alkadienes, http://linkedlifedata.com/resource/pubmed/chemical/Amides, http://linkedlifedata.com/resource/pubmed/chemical/Sulfides, http://linkedlifedata.com/resource/pubmed/chemical/propadiene
pubmed:status	MEDLINE
pubmed:month	Apr
pubmed:issn	1523-7052
pubmed:author	pubmed-author:ArmstrongAlanA, pubmed-author:EmmersonDaniel P GDP
pubmed:issnType	Electronic
pubmed:day	2
pubmed:volume	11
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1547-50
pubmed:meshHeading	pubmed-meshheading:19254002-Aldehydes, pubmed-meshheading:19254002-Alkadienes, pubmed-meshheading:19254002-Amides, pubmed-meshheading:19254002-Catalysis, pubmed-meshheading:19254002-Molecular Structure, pubmed-meshheading:19254002-Stereoisomerism, pubmed-meshheading:19254002-Sulfides
pubmed:year	2009
pubmed:articleTitle	Enantioselective synthesis of allenamides via sulfimide [2,3]-sigmatropic rearrangement.
pubmed:affiliation	Department of Chemistry, Imperial College London, South Kensington, London SW7 2AZ, UK.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't