16287281

Source:http://linkedlifedata.com/resource/pubmed/id/16287281

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0205250, umls-concept:C0443286
pubmed:issue	46
pubmed:dateCreated	2005-11-18
pubmed:abstractText	Asymmetric intramolecular Michael reaction catalyzed by an organocatalyst derived from cysteine has been developed for the synthesis of chiral bicyclo[4.3.0]nonene and cis-disubstituted cyclopentane skeletons with a creation of three or two contiguous chiral centers in good yield with high diastereo- and excellent enantioselectivities.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7503056
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Cysteine
pubmed:status	MEDLINE
pubmed:month	Nov
pubmed:issn	0002-7863
pubmed:author	pubmed-author:GotohHiroakiH, pubmed-author:HayashiYujiroY, pubmed-author:MasuiRyouheiR, pubmed-author:ShojiMitsuruM, pubmed-author:TamuraTomohiroT, pubmed-author:YamaguchiHirofumiH
pubmed:issnType	Print
pubmed:day	23
pubmed:volume	127
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	16028-9
pubmed:dateRevised	2008-1-17
pubmed:meshHeading	pubmed-meshheading:16287281-Catalysis, pubmed-meshheading:16287281-Cysteine, pubmed-meshheading:16287281-Molecular Structure, pubmed-meshheading:16287281-Stereoisomerism
pubmed:year	2005
pubmed:articleTitle	Cysteine-derived organocatalyst in a highly enantioselective intramolecular Michael reaction.
pubmed:affiliation	Department of Industrial Chemistry, Faculty of Engineering, Tokyo University of Science, Kagurazaka, Shinjuku-ku, Tokyo 162-8601, Japan. hyashi@ci.kagu.tus.ac.jp
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't