Convenient method for the synthesis of symmetrical disulfides using 1-butyl- 3-methylimidazolium hydroxide in water

نویسندگان

  • Soheil Sayyahi Department of Chemistry, Mahshahr Branch, Islamic Azad University, Mahshahr, Iran .E-mail: [email protected]
  • Somayeh Shagholi Department of Chemistry, Omidieh Branch, Islamic Azad University, Omidieh, Iran
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منابع مشابه

An efficient method for the preparation of symmetrical disulfides using 1-butyl- 3-methylimidazolium hydroxide in aqueous medium

In this study, a one-pot and efficient method is reported for the synthesis of symmetrical disulfides from alkyl halides in the present of sulfur and 1-butyl-3-methylimidazolium hydroxide as a basic reagent and phase transfer catalyst. The reaction proceeded very fast and afforded the desired products in moderate to excellent isolated yields.

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An efficient method for the preparation of symmetrical disulfides using 1-butyl- 3-methylimidazolium hydroxide in aqueous medium

In this study, a one-pot and efficient method is reported for the synthesis of symmetrical disulfides from alkyl halides in the present of sulfur and 1-butyl-3-methylimidazolium hydroxide as a basic reagent and phase transfer catalyst. The reaction proceeded very fast and afforded the desired products in moderate to excellent isolated yields.  

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Thermodynamic Study of the Ternary Electrolyte (1-Butyl-3-methylimidazolium chloride + sodium chloride + Water) System Using Potentiometric Measurements

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Highly efficient synthesis of carboacyclic nucleosides catalyzed by zinc oxide in 1-butyl-3-methylimidazolium bromide (ZnO/[bmim]Br)

Michael addition of pyrimidine and purine nucleobases to substituted as well as unsubstituted α,β-unsaturated esters efficiently proceeds in the presence of catalytic amount of zinc oxide in ionic liquid 1-butyl-3-methylimidazolium bromide (ZnO/[bmim]Br) under microwave irradiation to afford carboacyclic nucleosides, as biologically important compounds, in good to excellent yields and in short ...

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Highly efficient synthesis of carboacyclic nucleosides catalyzed by zinc oxide in 1-butyl-3-methylimidazolium bromide (ZnO/[bmim]Br)

Michael addition of pyrimidine and purine nucleobases to substituted as well as unsubstituted α,β-unsaturated esters efficiently proceeds in the presence of catalytic amount of zinc oxide in ionic liquid 1-butyl-3-methylimidazolium bromide (ZnO/[bmim]Br) under microwave irradiation to afford carboacyclic nucleosides, as biologically important compounds, in good to excellent yields and in short ...

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عنوان ژورنال

دوره 6  شماره 2

صفحات  27- 31

تاریخ انتشار 2016-11-01

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