Functional derivatives of thiophene. XIX. Synthesis and biological activity of some esters of 2-benzoylaminothiophene-3-carboxylic acids

1980 ◽  
Vol 14 (12) ◽  
pp. 861-863
Author(s):  
I. A. Kharizomenova ◽  
A. N. Grinev ◽  
N. V. Samsonova ◽  
N. V. Kaplina ◽  
M. V. Kapustina ◽  
...  
1981 ◽  
Vol 12 (21) ◽  
Author(s):  
I. A. KHARIZOMENOVA ◽  
A. N. GRINEV ◽  
N. V. SAMSONOVA ◽  
N. V. KAPLINA ◽  
M. V. KAPUSTINA ◽  
...  

2017 ◽  
Vol 87 (2) ◽  
pp. 224-230 ◽  
Author(s):  
I. A. Novakov ◽  
A. S. Yablokov ◽  
M. B. Navrotskii ◽  
A. S. Mkrtchyan ◽  
A. A. Vernigora ◽  
...  

1982 ◽  
Vol 37 (11-12) ◽  
pp. 1136-1140 ◽  
Author(s):  
Michael Entzeroth ◽  
Lothar Jaenicke

Abstract Some functional derivatives of blepharismone, the low-molecular conjugation hormone of Blepharisma japonicum, were synthesised and tested for their biological activity. The lipophilicity constant of the substituent in 5-position of the aromatic system directly correlates with the conjugation-inducing effect of this substance. Any change in the N-formyl-position leads to compounds less active than blepharismone, non-active or even inhibitory. Blepharismone-related kynurenine derivatives are inhibitors of the gamone activity depending on structural relationship.


1990 ◽  
Vol 55 (12) ◽  
pp. 2956-2962 ◽  
Author(s):  
Otomar Kříž ◽  
Zbyněk Plzák ◽  
Jaromír Plešek

Triethylamine borane, (C2H5)3N.BH3, is a stable, safe and readily available reagent which at 80 °C reduces carboxylic acids to primary alcohols in high yields; functional derivatives of carboxylic acids such as esters, nitriles or amides are virtually nonreactive with this reagent under the same conditions. Aldehydes, ketones and acid chlorides, however, react readily. No solvent is required for the process.


2018 ◽  
Vol 88 (7) ◽  
pp. 1397-1401
Author(s):  
M. V. Dmitriev ◽  
D. V. Ivanov ◽  
N. M. Igidov ◽  
R. R. Makhmudov ◽  
V. V. Novikova ◽  
...  

2013 ◽  
Vol 2013 ◽  
pp. 1-4 ◽  
Author(s):  
T. S. Zhivotova ◽  
R. E. Bakirova ◽  
S. D. Fazylov ◽  
S. K. Kabieva ◽  
T. V. Kryazheva

By reaction of 1,3,4-thiadiazol-2,5-dithiol with different organohalogens, chlorides of carboxylic acids, acrylic acid derivatives, alkaloids, and secondary amines, various derivatives of 2,5-bi-substituted 1,3,4-thiadiazole were synthesized, and biological properties of some of them were studied.


1992 ◽  
Vol 56 (10) ◽  
pp. 1623-1631 ◽  
Author(s):  
Hideki Uneme ◽  
Hiroyuki Mitsudera ◽  
Junji Yamada ◽  
Toshiya Kamikado ◽  
Yoshiaki Kono ◽  
...  

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