Literature DB >> 18068425

Catalytic reduction of pralidoxime in pharmaceuticals by macrocyclic Ni(II) compounds derived from orthophthalaldehyde.

P Muralidhar Reddy1, Adapa V S S Prasad, Rondla Rohini, Vadde Ravinder.   

Abstract

Efficient catalytic method for the reduction of pralidoxime to its amine derivative by macrocyclic Ni(II) compounds has been developed. Ten macrocyclic Schiff base Ni(II) compounds were synthesized via non-template synthesis by treating the corresponding macrocycles with nickel chloride in 1:1 ratio. The resulting compounds were characterized by elemental, IR, (1)H NMR, (13)C NMR, mass, electronic spectra, conductance, magnetic, thermal studies and their structures have been proposed. These compounds were used as catalysts for the reduction of pralidoxime to its amino derivative. The reduced pralidoxime was also characterized by spectral analysis and catalytic cycle has been established. The reduced product was determined spectrophotometrically by treating with ninhydrin reagent and the percent yields were found to be in the range of 75.12-82.36%.

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Year:  2007        PMID: 18068425     DOI: 10.1016/j.saa.2007.10.014

Source DB:  PubMed          Journal:  Spectrochim Acta A Mol Biomol Spectrosc        ISSN: 1386-1425            Impact factor:   4.098


  1 in total

1.  Synthesis, spectral and antibacterial sudies of copper(II) tetraaza macrocyclic complexes.

Authors:  Puchakayala Muralidhar Reddy; Rondla Rohini; Edulla Ravi Krishna; Anren Hu; Vadde Ravinder
Journal:  Int J Mol Sci       Date:  2012-04-19       Impact factor: 6.208

  1 in total

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