scholarly journals Synthesis of a New [3-(4-Chlorophenyl)-4-oxo-1,3-thiazolidin-5-ylidene]acetic Acid Derivative

Molbank ◽  
10.3390/m1150 ◽  
2020 ◽  
Vol 2020 (3) ◽  
pp. M1150
Author(s):  
Jacek Szczepański ◽  
Helena Tuszewska ◽  
Nazar Trotsko

The new methyl [3-(4-chlorophenyl)-2-{[(2,4-dichloro-1,3-thiazol-5-yl)methylidene]hydrazinylidene}-4-oxo-1,3-thiazolidin-5-ylidene]acetate was synthesized from 4-(4-chlorophenyl)-1-(2,4-dichloro-1,3-thiazol-5-yl)methylidene-3-thiosemicarbazide using dimethyl acetylenedicarboxylate as thia-Michael reaction acceptor. New compounds (3 and 4) were characterized by IR, 1H and 13C NMR spectroscopy methods.


Molbank ◽  
10.3390/m1140 ◽  
2020 ◽  
Vol 2020 (2) ◽  
pp. M1140
Author(s):  
Jack Bennett ◽  
Paul Murphy

(2S,3R,6R)-2-[(R)-1-Hydroxyallyl]-4,4-dimethoxy-6-methyltetrahydro-2H-pyran-3-ol was isolated in 18% after treating the glucose derived (5R,6S,7R)-5,6,7-tris[(triethylsilyl)oxy]nona-1,8-dien-4-one with (1S)-(+)-10-camphorsulfonic acid (CSA). The one-pot formation of the title compound involved triethylsilyl (TES) removal, alkene isomerization, intramolecular conjugate addition and ketal formation. The compound was characterized by 1H and 13C NMR spectroscopy, ESI mass spectrometry and IR spectroscopy. NMR spectroscopy was used to establish the product structure, including the conformation of its tetrahydropyran ring.



ChemInform ◽  
2010 ◽  
Vol 22 (49) ◽  
pp. no-no
Author(s):  
P. E. GEORGHIOU ◽  
C. K. HO ◽  
C. R. JABLONSKI


ChemInform ◽  
2010 ◽  
Vol 24 (30) ◽  
pp. no-no
Author(s):  
J. LAYNEZ ◽  
M. MENENDEZ ◽  
J. L. SAIZ VELASCO ◽  
A. L. LLAMAS-SAIZ ◽  
C. FOCES-FOCES ◽  
...  


2021 ◽  
Vol 3 ◽  
pp. 119-127
Author(s):  
G.M. Baisarov ◽  
◽  
S.M. Adekenov ◽  

The reaction of 5-hydroxy-7-methoxy-2-phenylchroman-4-one with dibromoalkanes in acetone in the presence of potassium carbonate proceeds according to the Michael’s retro-reaction O-alkylation and leads to the formation of the corresponding 2-(bromo-alkoxy) chalcones. The structure of the synthesized compounds was confirmed by IR-, 1H- and 13C-NMR spectroscopy. The cytotoxic, hepatoprotective and anti-inflammatory effects of chalcone derivatives (2-3) were studied for the first time in vitro and in vivo.



2002 ◽  
Vol 228 (2) ◽  
pp. 163-173 ◽  
Author(s):  
A. Bodor ◽  
I. Bányai ◽  
L. Zékány ◽  
I. Tóth


2002 ◽  
Vol 602-603 ◽  
pp. 321-333 ◽  
Author(s):  
Masatoshi Kobayashi ◽  
Shigeki Kuroki ◽  
Isao Ando ◽  
Kazuo Yamauchi ◽  
Hideaki Kimura ◽  
...  


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