2741-13-1Relevant articles and documents
Method for preparing aryl isothiourea
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Paragraph 0037, (2021/12/07)
The invention discloses a method for preparing aryl isothiourea, wherein hydride is suspended in a solvent, and thiourea is sequentially added. O diiodo benzene followed by reaction to prepare aryl isothiosemicarbazone. The isothiourea structure is widely
Insertion of arynes into thioureas: A new amidine synthesis
Biswas, Kallolmay,Greaney, Michael F.
supporting information; experimental part, p. 4946 - 4949 (2011/11/06)
Arynes, generated from trimethylsilyl phenyltriflate precursors, have been found to react with thioureas via a formal π-insertion into the C=S bond. The reaction contrasts with that of ureas, which proceeds via benzyne σ-insertion into the C-N bond, and r
Reaction of 1,4,2-Dithiazolium Salts with Amino Compounds
Yonemoto, Katsumi,Shibuya, Isao
, p. 4043 - 4050 (2007/10/02)
Systematic studies on the behavior of 1,4,2-dithiazolium cations (1) toward various amino compounds (ammonia, aliphatic and aromatic amines, hydrazine, semicarbazide, thiosemicarbazide derivatives, etc.) were performed.The reaction pathway could be classified into three types depending on possibile three fission modes of the initially-formed adduct.The main products were 5-imino-1,4,2-dithiazole, thiourea, and 1,3,4-thiadiazole derivatives, through the three different pathways, respectively.In order to clarify the factors controlling the reaction courses, the reactions of 1 with p-substituted aniline derivatives were carried out under systematically varying conditions.The strength of bases and the polaritiy of solvents had clear influence on the reactivity.The reaction mechanism is also discussed.