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pubmed-article:12050436rdf:typepubmed:Citationlld:pubmed
pubmed-article:12050436pubmed:issuePt 6lld:pubmed
pubmed-article:12050436pubmed:dateCreated2002-6-6lld:pubmed
pubmed-article:12050436pubmed:abstractTextThe structure of the title S-alkylated isothiosemicarbazide, C(12)H(15)N(3)OS, was determined by single-crystal diffractometry and compared with the structures of other compounds containing the S-alkylthiosemicarbazide moiety. Such structures cluster into two groups, according to the different orientation of the [bond]SR group with respect to the hydrazine N atom of the thiosemicarbazide. The cis arrangement is preferred by most molecules in the solid state, in spite of the possibility of intramolecular N[bond]H...N interactions in the opposite orientation.lld:pubmed
pubmed-article:12050436pubmed:languageenglld:pubmed
pubmed-article:12050436pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:12050436pubmed:statusPubMed-not-MEDLINElld:pubmed
pubmed-article:12050436pubmed:monthJunlld:pubmed
pubmed-article:12050436pubmed:issn0108-2701lld:pubmed
pubmed-article:12050436pubmed:authorpubmed-author:ForniAlessand...lld:pubmed
pubmed-article:12050436pubmed:authorpubmed-author:GradinaruJuli...lld:pubmed
pubmed-article:12050436pubmed:issnTypePrintlld:pubmed
pubmed-article:12050436pubmed:volume58lld:pubmed
pubmed-article:12050436pubmed:ownerNLMlld:pubmed
pubmed-article:12050436pubmed:authorsCompleteYlld:pubmed
pubmed-article:12050436pubmed:paginationo342-4lld:pubmed
pubmed-article:12050436pubmed:dateRevised2003-11-3lld:pubmed
pubmed-article:12050436pubmed:year2002lld:pubmed
pubmed-article:12050436pubmed:articleTitle1-(1-Benzoylpropen-2-yl)-3-methylisothiosemicarbazide.lld:pubmed
pubmed-article:12050436pubmed:affiliationCNR - Istituto di Scienze e Tecnologie Molecolari, Via Golgi 19, I-20133 Milano, Italy. a.forni@istm.cnr.itlld:pubmed
pubmed-article:12050436pubmed:publicationTypeJournal Articlelld:pubmed