Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Tiruhi A. Gomktsyan"'
Autor:
Vergush A. Pivazyan, Emma A. Ghazaryan, Armen V. Karapetyan, Roza S. Shainova, Siranush V. Harutyunyan, Asya S. Vorskanyan, Aleksandr P. Yengoyan, Tiruhi A. Gomktsyan
Publikováno v:
Journal of Saudi Chemical Society, Vol 27, Iss 3, Pp 101628- (2023)
Ultrasound-assisted green syntheses of novel potentially bioactive pyrimidine derivatives have been carried out. The same compounds were obtained by conventional methods of synthesis, and the reaction times and yields of final products obtained by th
Externí odkaz:
https://doaj.org/article/1ed104bd41b24049879266bd07d3dbcf
Publikováno v:
Russian Journal of General Chemistry. 90:1181-1187
New derivatives of a number of aryloxy and arylaminopropanehydrazides were synthesized. Their heterocyclization under the action of carbon disulfide and potassium hydroxide and subsequent alkylation of the resulting 2-thioxo-1,3,4-oxadiazole ring, th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bcf5d03eab5a31a54f6e9b66abca15d7
https://doi.org/10.1134/s1070363220070014
https://doi.org/10.1134/s1070363220070014
Publikováno v:
Journal of Chemical Research. 44:271-276
The affordable and efficient methods for the syntheses of acyclic derivatives of 2-(3-(3,5-dimethyl-1H-pyrazol-1-yl)-6-oxopyridazin-1(6H)-yl)acetohydrazine as well as compounds with a combination of pyrazolyl-pyridazine fragment with various azoles i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff097f896805ec36f89e069f6cb9fff0
https://doi.org/10.1177/1747519819897523
https://doi.org/10.1177/1747519819897523
Publikováno v:
Journal of Chemical Research. 43:352-358
On the basis of 2-benzyl-6-hydroxypyridazin-3(2 H)-one, a series of its novel O-substituted (including 6-(1,3,5-triazin-2-yl)oxy) derivatives is prepared. It is proven that the substitution reactions in the initial compound occur mainly at the oxygen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e73468b004aa1f2199c8339272428107
https://doi.org/10.1177/1747519819866402
https://doi.org/10.1177/1747519819866402
Publikováno v:
Journal of Chemical Research. 42:535-539
Simple and accessible pathways for the synthesis of a series of novel 6-(3,5-dimethyl-1H-pyrazol-1-yl)pyridazin-3(2H)-one derivatives including compounds with a combination of a pyrazolyl-pyridazine moiety with pyrimidine, 1,3,5-triazine and 1,3,4-ox
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::628cae2c1e98d1f16d1d1ef8ef0ee089
https://doi.org/10.3184/174751918x15389922302823
https://doi.org/10.3184/174751918x15389922302823
Publikováno v:
Journal of Chemical Research. 41:205-209
The syntheses of a series of novel compounds with a combination of pyrazole and pyridazine rings and their corresponding pyrazolyl-1-N-substituted derivatives were carried out. These rings are connected through the oxygen atom and oxoethoxy or oxoeth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5d7df2efbb70642c8f757f2f0375a8e
https://doi.org/10.3184/174751917x14894997017531
https://doi.org/10.3184/174751917x14894997017531
Supplemental material, SUPPLEMENTARY_MATERIAL-Shainova for Synthesis and biological evaluation of 3-O-substituted 1-benzyl-6-oxo-1,6-dihydropyridazine derivatives by Roza S Shainova, Tiruhi A Gomktsyan, Armen V Karapetyan and Aleksandr P Yengoyan in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6501430e6f499b177aa69b72fd8696cd
Autor:
S. G. Tiratsuyan, Tiruhi A. Gomktsyan, A. A. Hovhannisyan, Armen V. Karapetyan, A. P. Yengoyan
Publikováno v:
Russian Journal of Plant Physiology. 63:656-662
A series of pyridazine derivatives was synthesized and some of them showed a growth stimulatory activity during preliminary screening. Their effects on germination, morphogenesis, peroxidase activity and lignan content were tested on common bean (Pha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba5efebdaccb8f108c8af583e57cadb5
https://doi.org/10.1134/s1021443716050125
https://doi.org/10.1134/s1021443716050125