Setembro 2013 vol. 1 num. 1 - Brazilian Meeting on Organic Synthesis 2011

Abstract - Open Access.

Idioma principal

Microwave-assisted one-pot synthesis of symmetrical dichalcogenides catalyzed by CuO nanopowder

Botteselle, Giancarlo V. ; Godoi, Marcelo ; Galetto, Fábio Z. ; Singh, Devender ; Bettanin, Luana ; Braga, Antonio Luiz ;

Abstract:

Over last few decades, organochalcogen (S, Se and Te) compounds have attracted important roles as reagents and synthetic intermediates in organic synthesis. Organodichalcogenides of sulfur, selenium or tellurium in counterpart of organic peroxides, play an important role in organochalcogen chemistry since they are stable, easy to handle, and reactive enough to produce eletrophilic, nucleophilic and radicophilic species. In addition showed important biological activities, such as antioxidants and antitumor. Recently we developed a new methodology to synthesis a wide range of organodiselenides and ditelurides, through cross-coupling reaction of selenium or tellurium and aryl halides using CuO nanopowder as catalyst. So we describe here an improved microwaveassisted method to prepare organodiselenides, ditelurides and disulfides using CuO nanoparticles as catalyst.

Abstract:

Palavras-chave: Organodichalcogenides, Microwave, CuO nano,

Palavras-chave: ,

DOI: 10.5151/chempro-14bmos-R0161-1

Referências bibliográficas
  • [1] 1 Rheinboldt, H. Sulfur-, Selenium-, Tellurium-Compounds, Methoden Org. Chem. (Houben-Weyl) 1967, 9.
  • [2] 2 Nogueira, C. W.; Zeni, G.; Rocha, J. B. T. Chem. Rev. 2004, 104, 6255.
  • [3] 3 Singh, D.; Deobald, A. M.; Camargo, L. R. S.; Tabarelli, G.; Rodrigues, O. E. D.; Braga, A. L. Org. Lett. 2010, 12, 3288.
Como citar:

Botteselle, Giancarlo V.; Godoi, Marcelo; Galetto, Fábio Z.; Singh, Devender; Bettanin, Luana; Braga, Antonio Luiz; "Microwave-assisted one-pot synthesis of symmetrical dichalcogenides catalyzed by CuO nanopowder", p. 161 . In: In Blucher Chemistry Proceedings, São Paulo, v. 1, n. 1, Setembro.2013. São Paulo: Blucher, 2013.
ISSN 2318-4043, DOI 10.5151/chempro-14bmos-R0161-1

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