highly efficient synthesis of carboacyclic nucleosides catalyzed by zinc oxide in 1-butyl-3-methylimidazolium bromide (zno/[bmim]br)

Authors

tarlan salehi-hamzehkhani

marzieh hatami

abdolkarim zare

ahmad reza moosavi-zare

abolfath parhami

abstract

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 reaction times.

Upgrade to premium to download articles

Sign up to access the full text

Already have an account?login

similar resources

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 ...

full text

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 ...

full text

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 text

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 text

NMR 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...

full text

My Resources

Save resource for easier access later


Journal title:
iranian journal of catalysis

Publisher: islamic azad university, shahreza branch

ISSN 2252-0236

volume 4

issue 4 2014

Keywords
[ ' c a r b o a c y c l i c n u c l e o s i d e ' , ' m i c h a e l a d d i t i o n ' , ' z i n c o x i d e ' , ' i o n i c l i q u i d ' , 1 , ' b u t y l ' , 3 , ' m e t h y l i m i d a z o l i u m b r o m i d e ( [ b m i m ] b r ) ' , ' m i c r o w a v e i r r a d i a t i o n ' ]

Hosted on Doprax cloud platform doprax.com

copyright © 2015-2023