Zobrazeno 1 - 10
of 40
pro vyhledávání: '"I. L. Aleksanyan"'
Autor:
I. L. Aleksanyan, L. P. Hambardzumyan
Publikováno v:
Russian Journal of Organic Chemistry. 56:2114-2118
Quinolinyl-substituted five-membered heterocyclic compounds containing 1,3,4-oxadiazole, 1,3-dioxoisoindole, 1,2,4-triazole, and 1,3,4-thiadiazole rings and Schiff bases were synthesized starting from 2-(4-hydroxy-2-methylquinolin-3-yl)acetohydrazide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13dff9330a6d3451955463e3133096ac
https://doi.org/10.1134/s1070428020120118
https://doi.org/10.1134/s1070428020120118
Autor:
L. P. Hambardzumyan, I. L. Aleksanyan
Publikováno v:
Russian Journal of Organic Chemistry. 56:261-264
Novel hetarylquinolines containing 1,3,4-oxadiazole and 1,3-dioxoisoindoline rings and Schiff base residues were synthesized on the basis of 2-[(4-methylquinolin-2-yl)sulfanyl]acetohydrazides substituted in the benzene ring.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5ee0ba48fb595ab6a879ee96940f967
https://doi.org/10.1134/s107042802002013x
https://doi.org/10.1134/s107042802002013x
Autor:
I. L. Aleksanyan, L. P. Hambardzumyan
Publikováno v:
Russian Journal of Organic Chemistry. 55:262-265
A substituted quinoline-6-carbohydrazide was synthesized by the reaction of ethyl 4-hydroxy-2-methylquinoline-6-carboxylate with hydrazine hydrate. The quinoline-6-carbohydrazide was reacted with phenyl isothiocyanate to obtain the corresponding phen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::89ebc4d8f0f5033383682cbb78928b5e
https://doi.org/10.1134/s1070428019020209
https://doi.org/10.1134/s1070428019020209
Autor:
L. P. Hambardzumyan, I. L. Aleksanyan
Publikováno v:
Russian Journal of Organic Chemistry. 54:1402-1405
Intramolecular cyclization of 2-{[(4-methyl(or 4,6- and 4,8-dimethyl)quinolin-2-yl)sulfanyl]-acetyl}-N-phenylhydrazine-1-carbothioamides in alkaline and acidic media afforded {[(4-methyl(or 4,6- and 4,8-dimethyl)quinolin-2-yl)sulfanyl]acetyl}-substit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd556a854385273c6bcf782a4de984a0
https://doi.org/10.1134/s1070428018090221
https://doi.org/10.1134/s1070428018090221
Autor:
I. L. Aleksanyan, L. P. Hambardzumyan
Publikováno v:
Russian Journal of Organic Chemistry. 55:399-401
Thiazolidine and thiazolidinone derivatives containing a quinoline fragment have been synthesized by heterocyclizations of 4-(2-hydroxy-4-methylquinolin-3-yl)butan-2-one thiosemicarbazones with bromoacetophenone and ethyl bromoacetate.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f4b891afe1ae1a7d4edf63fddb70104
https://doi.org/10.1134/s1070428019030242
https://doi.org/10.1134/s1070428019030242
Autor:
L. P. Hambardzumyan, I. L. Aleksanyan
Publikováno v:
Russian Journal of Organic Chemistry. 53:226-230
At intramolecular cyclization of phenylhydrazinocarbothioamide in alkaline and acidic media quinolyl-substituted triazoles and thiadiazoles are obtained. Quinolyl-substituted thiazolidines and thiazolidinones were obtained at interaction of phenylhyd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f01f97f594fafb2767bf3f53675fbcfb
https://doi.org/10.1134/s1070428017020142
https://doi.org/10.1134/s1070428017020142
Autor:
L. P. Ambartsumyan, I. L. Aleksanyan
Publikováno v:
Russian Journal of Organic Chemistry. 51:1046-1049
Heterocyclic thiosemicarbazones and thiosemicarbazides, including quinoline derivatives, are polyfunctional substrates that are widely used in the development of methods for the synthesis of biologically active compounds which may be promising as med
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a4bee4dadfbc592286a159891577c41
https://doi.org/10.1134/s1070428015070301
https://doi.org/10.1134/s1070428015070301
Autor:
L. P. Ambartsumyan, I. L. Aleksanyan
Publikováno v:
Russian Journal of Organic Chemistry. 49:559-562
2-(Hydroxyphenylamino)- and 2-(aminophenylamino)-4-methylquinolines and N,N′-bis(4-methylquinolin-2-yl)benzenediamines were synthesized by reactions of 2-chloro-4-methylquinolines with o-, m-, and p-aminophenols and o-, m-, and p-phenylenediamines.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2cb21c1451e05c897d5b9a11febf769
https://doi.org/10.1134/s1070428013040118
https://doi.org/10.1134/s1070428013040118
Autor:
I. L. Aleksanyan, L. P. Hambardzumyan
Publikováno v:
Russian Journal of Organic Chemistry. 50:442-444
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::04a52719866109f345a98776dc06d40f
https://doi.org/10.1134/s1070428014030257
https://doi.org/10.1134/s1070428014030257
Publikováno v:
Russian Journal of Organic Chemistry. 46:571-576
A procedure has been developed for the synthesis of (2-methylquinolin-4-ylsulfanyl)-substituted acetic and propionic acids and propionitriles having methyl, methoxy, or carboxy groups or halogen atom in position 6 or 8 of the quinoline ring via react
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9bbbb08f0133f0ca859e7b87973cb2f5
https://doi.org/10.1134/s1070428010040226
https://doi.org/10.1134/s1070428010040226