Synthesis and Biological Activity of Novel Ethyl Esters of 4-R-6,8-Dimethyl-1-oxo-1,2-dyhidropyrrolo[1,2-d][1,2,4]triazine-7-carboxylic Acids

2015 ◽  
Vol 53 (2) ◽  
pp. 421-428 ◽  
Author(s):  
Valeriia Astakhina ◽  
Maxim Voievudskyi ◽  
Olexander Kharchenko ◽  
Vladimir Novikov ◽  
Elena Komarovska-Porohnyavets ◽  
...  
ChemInform ◽  
2016 ◽  
Vol 47 (31) ◽  
Author(s):  
Valeriia Astakhina ◽  
Maxim Voievudskyi ◽  
Olexander Kharchenko ◽  
Vladimir Novikov ◽  
Elena Komarovska-Porohnyavets ◽  
...  

2012 ◽  
Vol 67 (3-4) ◽  
pp. 123-128
Author(s):  
Anna Pachuta-Stec ◽  
Urszula Kosikowska ◽  
Anna Chodkowska ◽  
Monika Pitucha ◽  
Anna Malm ◽  
...  

N-Substituted amides of endo-3-(3-methylthio-1,2,4-triazol-5-yl)bicyclo[2.2.1]hept-5-ene- 2-carboxylic acid and 1-(5-methylthio-1,2,4-triazol-3-yl)cyclohexane-2-carboxylic acid were prepared by the condensation reaction of endo-S-methyl-N1-(bicyclo[2.2.1]hept-5-ene-2,3- dicarbonyl)isothiosemicarbazide and S-methyl-N1-(cyclohexane-2,3-dicarbonyl)isothiosemicarbazide with primary amines. The synthesized compounds were screened for their microbiological and pharmacological activities


1970 ◽  
Vol 48 (11) ◽  
pp. 1689-1697 ◽  
Author(s):  
M. W. Roomi ◽  
S. F. MacDonald

Ethyl esters of 2-alkyl- and 2,4-dialkylpyrrole-3-carboxylic acids are obtained generally by extensions of the Hantzsch synthesis, benzyl and t-butyl esters when the 2-alkyl group is methyl. Hemopyrrole is obtained from butanal and ethyl acetoacetate in three steps. Pyrroles bearing higher alkyl groups or carbobenzoxy groups are reductively alkylated like the corresponding methylpyrroles and carbethoxy derivatives; t-butyl esters do not survive.


ChemInform ◽  
2010 ◽  
Vol 22 (27) ◽  
pp. no-no
Author(s):  
S. E. HAGEN ◽  
J. M. DOMAGALA ◽  
C. L. HEIFETZ ◽  
J. JOHNSON

2019 ◽  
Vol 89 (5) ◽  
pp. 1051-1054
Author(s):  
A. A. Aghekyan ◽  
G. G. Mkryan ◽  
A. S. Tsatinyan ◽  
G. V. Gasparyan

ChemInform ◽  
2010 ◽  
Vol 22 (19) ◽  
pp. no-no
Author(s):  
C. B. JUN. ZIEGLER ◽  
N. A. KUCK ◽  
T. W. STROHMEYER ◽  
Y. -I LIN

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