Structural and dynamical characterization of piroxicam by 1H- and 13C-NMR relaxation studies

1987 ◽  
Vol 27 (3) ◽  
pp. 255-261 ◽  
Author(s):  
Claudio Rossi ◽  
Adriana Casini ◽  
Maria Pia Picchi ◽  
Franco Laschi ◽  
Angela Calabria ◽  
...  
1977 ◽  
Vol 50 (1) ◽  
pp. 49-62 ◽  
Author(s):  
M. M. Coleman ◽  
D. L. Tabb ◽  
E. G. Brame

Abstract 13C NMR spectroscopy has proved to be a very powerful tool for the characterization of polychloroprene microstructure. We have identified and assigned the lines associated with diad and triad sequences involving the predominant trans-1,4 placement, together with other lines associated with cis-1,4, 1,2, isomerized 1,2, and 3,4 structural irregularities. Currently, we are performing 13C NMR, relaxation studies on the chloroprene polymers and will be presenting quantitative data in the near future.


2015 ◽  
Vol 77 (3) ◽  
Author(s):  
Helmi Mohammed Al-Maqtari ◽  
Joazaizulfazli Jamalis ◽  
Hasnah Mohd Sirat

Heterocyclic chalcones containing halogenated thiophenes were synthesized. The first step was to synthesize 3-acetyl-2,5-dichlorothiophene and 2-acetyl-5-chlorothiophene as heterocyclic ketones by using Friedel-Crafts acylation. The ketones were then used to synthesize thiophene chalcones through Claisen-Schmidt reaction with the respective heterocyclic aldehydes such as 5-bromothiophene-2-carbaldehyde, 3-methyl-2-thiophene carboxaldehyde and 2-thiophene carboxaldehyde with 3-acetyl-2,5-dichlorothiophene or 2-acetyl-5-chlorothiophene in presence of basic medium, sodium hydroxide to form the corresponding chalcones. Structures of the synthetic compounds were confirmed by IR, MS, 1H and 13C NMR spectral data.


2019 ◽  
Vol 84 (4) ◽  
pp. 343-353
Author(s):  
Lina Rekovic ◽  
Lidija Kosychova ◽  
Irina Bratkovskaja ◽  
Regina Vidziunaite

Three new 1,3,4,5-tetrahydro-2H-1,5-benzodiazepin-2-one oximes were synthesized and characterized by the methods of 1H- and 13C-NMR, IR and elemental analysis. Along with previously described compounds bearing one additional methyl group on the 5th nitrogen atom, the new compounds were characterized in bulk by UV?Vis and fluorescence spectroscopy in various solvents. The influence of the nature of the organic solvent on the spectra of the title compounds was investigated and is discussed.


2016 ◽  
Vol 266 ◽  
pp. 23-40 ◽  
Author(s):  
Pavel Kadeřávek ◽  
Vojtěch Zapletal ◽  
Radovan Fiala ◽  
Pavel Srb ◽  
Petr Padrta ◽  
...  

Chemosphere ◽  
2018 ◽  
Vol 199 ◽  
pp. 201-209 ◽  
Author(s):  
Sepehr Shakeri Yekta ◽  
Mattias Hedenström ◽  
Jan Eric Stehr ◽  
Mårten Dario ◽  
Norbert Hertkorn ◽  
...  

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