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Convenient diastereoselective synthesis of annulated 3-substituted-(5S*,6S*,Z)-2-(2-(2,4-dinitrophenyl)hydrazono)-5,6-diphenyl-1,3-thiazinan-4-ones.
Hassan, Alaa A; Mohamed, Nasr K; Aly, Ashraf A; Tawfeek, Hendawy N; Hopf, Henning; Bräse, Stefan; Nieger, Martin.
  • Hassan AA; Chemistry Department, Faculty of Science, Minia University, El-Minia, 61519, Egypt. alaahassan2001@mu.edu.eg.
  • Mohamed NK; Chemistry Department, Faculty of Science, Minia University, El-Minia, 61519, Egypt.
  • Aly AA; Chemistry Department, Faculty of Science, Minia University, El-Minia, 61519, Egypt.
  • Tawfeek HN; Chemistry Department, Faculty of Science, Minia University, El-Minia, 61519, Egypt.
  • Hopf H; Institut für Organische Chemie, Technische Universität Braunschweig, 38092, Brunswick, Germany.
  • Bräse S; Institute of Organic Chemistry, Karlsruhe Institute of Technology, Fritz-Haber-Weg 6, 76131, Karlsruhe, Germany.
  • Nieger M; Department of Chemistry, University of Helsinki, A. I. Virtasen aukio I, P.O. Box 55, 00014, Helsinki, Finland.
Mol Divers ; 23(4): 821-828, 2019 Nov.
Article en En | MEDLINE | ID: mdl-30607761
ABSTRACT
Racemic 2-(2,4-dinitrophenyl)hydrazono)-5,6-diphenyl-1,3-thiazinan-4-ones and (Z)-N'-(2,4-dinitrophenyl)-2,3-diphenylacrylohydrazide were formed during the diastereoselective reaction between 4-substituted 1-(2,4-dinitrophenyl)thiosemicarbazides and 2,3-diphenylcycloprop-2-enone under refluxing ethanol. The structures of the synthesized compounds were confirmed by single-crystal X-ray analyses.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Tiazoles Idioma: En Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Tiazoles Idioma: En Año: 2019 Tipo del documento: Article