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pubmed-article:21578448rdf:typepubmed:Citationlld:pubmed
pubmed-article:21578448pubmed:issuePt 11lld:pubmed
pubmed-article:21578448pubmed:dateCreated2011-5-17lld:pubmed
pubmed-article:21578448pubmed:abstractTextThe title compound, C(15)H(16)ClNO(3)S, was obtained by the organocatalytic asymmetric Michael addition of thian-4-one to 1-chloro-4-[(1E,3E)-4-nitro-buta-1,3-dien-yl]benzene. The double bond has an E configuration and the thian-4-one six-membered ring adopts a chair conformation. The crystal structure is stabilized by weak inter-molecular C-H?O hydrogen bonds.lld:pubmed
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pubmed-article:21578448pubmed:languageenglld:pubmed
pubmed-article:21578448pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:21578448pubmed:statusPubMed-not-MEDLINElld:pubmed
pubmed-article:21578448pubmed:issn1600-5368lld:pubmed
pubmed-article:21578448pubmed:authorpubmed-author:GuoYiYlld:pubmed
pubmed-article:21578448pubmed:authorpubmed-author:WangYifengYlld:pubmed
pubmed-article:21578448pubmed:authorpubmed-author:LiZhaoboZlld:pubmed
pubmed-article:21578448pubmed:authorpubmed-author:LuoShupingSlld:pubmed
pubmed-article:21578448pubmed:issnTypeElectroniclld:pubmed
pubmed-article:21578448pubmed:volume65lld:pubmed
pubmed-article:21578448pubmed:ownerNLMlld:pubmed
pubmed-article:21578448pubmed:authorsCompleteYlld:pubmed
pubmed-article:21578448pubmed:paginationo2861lld:pubmed
pubmed-article:21578448pubmed:dateRevised2011-11-11lld:pubmed
pubmed-article:21578448pubmed:year2009lld:pubmed
pubmed-article:21578448pubmed:articleTitle(S)-3-[(S,E)-4-(4-Chloro-phen-yl)-1-nitro-but-3-en-2-yl]thian-4-one.lld:pubmed
pubmed-article:21578448pubmed:affiliationState Key Laboratory Breeding Base of Green Chemistry-Synthesis Technology, Zhejiang University of Technology, Hangzhou 310014, People's Republic of China.lld:pubmed
pubmed-article:21578448pubmed:publicationTypeJournal Articlelld:pubmed