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Structure of Products of Reaction between Benzoylacetylene and 1,5-Diphenyldithiobiuret.
- Source :
- Chemistry of Heterocyclic Compounds; Jan2002, Vol. 38 Issue 1, p74-78, 5p
- Publication Year :
- 2002
-
Abstract
- Reaction of benzoylacetylene with 1,5-diphenyldithiobiuret in glacial AcOH in the presence of equimolar amounts of HClO<subscript>4</subscript> leads exclusively to 2-benzoylmethyl-4,6-di(phenylimino)-1,3,5-dithiazinium perchlorate. In MeOH, benzene, and MeCN medium, the reaction proceeds nonselectively and a mixture is formed that includes 2-benzoylmethyl-4,6-di(phenylimino)-1,3,5-dithiazine, 2-benzoylmethyl-4-benzoylvinylthio-3-phenyl-6-phenylimino-1,3,5-thiadiazine, 2-benzoylmethyl-4,6-di-(thiocarbonyl)-1,3-diphenyl-1,3,5-triazine, and N-benzoylvinyl-N'-phenylthiourea. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 00093122
- Volume :
- 38
- Issue :
- 1
- Database :
- Complementary Index
- Journal :
- Chemistry of Heterocyclic Compounds
- Publication Type :
- Academic Journal
- Accession number :
- 49910456
- Full Text :
- https://doi.org/10.1023/A:1014859410679