1-Butyl-3-Methylimidazolium Bromide Promoted Selectively Oxidation of Sulfur Compounds by NaBrO3
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Abstract:
1-Butyl-3-methylimidazolium bromide ([bmim]Br) as an ionic liquid promoted selectively oxidation of aliphatic and aromatic sulfides to the corresponding sulfoxides and the oxidative coupling of thiols to disulfides by NaBrO3 in excellent yields under neutral conditions.
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1-butyl-3-methylimidazolium bromide promoted selectively oxidation of sulfur compounds by nabro3
1-butyl-3-methylimidazolium bromide ([bmim]br) as an ionic liquid promoted selectively oxidation of aliphatic and aromatic sulfides to the corresponding sulfoxides and the oxidative coupling of thiols to disulfides by nabro3 in excellent yields under neutral conditions.
full textHighly 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 ...
full textHighly 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 ...
full textUltrasound-promoted Catalyst-free Synthesis of α-Aminonitriles in 1-Butyl-3-methylimidazolium Bromide ([Bmim]Br) as a Reusable Neutral Ionic Liquid
A catalyst-free one-pot three component methodology for the synthesis of α-aminonitriles under ultrasonic irradiation at room temperature using [Bmim]Br as a neutral reaction medium is described. A broad range of substrates including the aromatic, heteroaromatic and aliphatic aldehydes were condensed with amines (aliphatic and aromatic) and trimethylsilyl cyanide (TMSCN). Using this method, all...
full texthighly 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 ...
full textNMR study for self-aggregation of 1-butyl-3-methylimidazolium bromide in aqueous solution.
Self-aggregation of 1-butyl-3-methylimidazolium bromide ([bmim]Br) in D(2)O has been investigated using NMR spectroscopy. The (1)H spin-lattice relaxation times (T(1)) of the [bmim](+) increased with the decrease of concentration in the range of 0.1-3.0 mol dm(-3) as expected, however, in contrast, the (1)H-T(1) decreased below 0.1 mol dm(-3). The estimated (13)C-activation energies indicated t...
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Journal title
volume 31 issue 1
pages 1- 8
publication date 2012-03-01
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