Zobrazeno 1 - 10
of 68
pro vyhledávání: '"R. G. Dubenko"'
Publikováno v:
Chemistry of Heterocyclic Compounds. 11:567-570
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2b3971c8183ee3c7b36c01247dcc197
https://doi.org/10.1007/bf00480480
https://doi.org/10.1007/bf00480480
Publikováno v:
Chemistry of Heterocyclic Compounds. 7:563-566
Substituted 1-(3-methyl-2-benzothiazolinidenyl)-5-(phenylaminothiocarbo)thiocarbohydrazides are cyclized under the influence of potassium ferricyanide, hydrogen peroxide, or ferric chloride to substituted 1-(3-methyl-2-benzothiazolinidenyl)-5-(2-benz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd8769ca76fa0474f2c3a01a5facd7eb
https://doi.org/10.1007/bf00945492
https://doi.org/10.1007/bf00945492
Publikováno v:
Chemistry of Heterocyclic Compounds. 6:1114-1117
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a9348dd856cf1526a6d622c56f9a271
https://doi.org/10.1007/bf00480718
https://doi.org/10.1007/bf00480718
Publikováno v:
Chemistry of Heterocyclic Compounds. 7:121-124
Cyanoethylation of 4-aryl-5-arylamino-1,2,4-triazoline-3-thiones proceeds at the nitrogen atom of the thioamide group. Alkylation of 4-aryl-5-arylamino-1,2,3-triazoline-3-thiones with chloroacetonitrile, monochloroacetic acid and its ester, Β-chloro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::22c9c66f8931a20783ca46a0e36cfdfa
https://doi.org/10.1007/bf00477966
https://doi.org/10.1007/bf00477966
Autor:
E. F. Gorbenko, R. G. Dubenko
Publikováno v:
Chemistry of Heterocyclic Compounds. 3:727-730
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17d413a715c25be92248c1c72a2e3fd5
https://doi.org/10.1007/bf00468360
https://doi.org/10.1007/bf00468360
Autor:
E. F. Gorbenko, R. G. Dubenko
Publikováno v:
Chemistry of Heterocyclic Compounds. 10:434-436
3-Arylamino-4-cyano-5-phenylpyrazoles and 3-aryl-4-phenyl-2-[(benzoyl)cyanomethyl-ene]-4, 5-thiazolines, respectively, were obtained by condensation of benzoylcyanothioacetic acid arylamides with hydrazine hydrate or withΩ-bromoacetophenone. 2-[(Ben
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f32159dcc9b2de40f6418dd3226b6407
https://doi.org/10.1007/bf00945634
https://doi.org/10.1007/bf00945634
Autor:
E. F. Gorbenko, R. G. Dubenko
Publikováno v:
Chemistry of Heterocyclic Compounds. 11:301-303
Substituted 2-benzalhydrazono-3-phenyl-4-(arylhydrazonochloroformyl)-4-thiazo-lines and 2,2′-azinobis[3-aryl-4-(arylhydrazonochloroformyl)-4-thiazolines], respectively, are formed in the condensation of arylhydrazones of chloromethylgly-oxyloyl chl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a7d1c6c129fdf0e41cf01a499127ef9
https://doi.org/10.1007/bf00470074
https://doi.org/10.1007/bf00470074
Publikováno v:
Theoretical and Experimental Chemistry. 2:318-320
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b25f88ef2b6ef54474f27d07f6d74012
https://doi.org/10.1007/bf00533808
https://doi.org/10.1007/bf00533808
Publikováno v:
Chemistry of Heterocyclic Compounds. 5:551-553
The reaction of arylhydrazones of ethyl cyanoglyoxylate with hydroxylamine hydrochloride in aqueous ethanolic solution in the presence of sodium acetate at the boil has given 3-amino-4-arylazoisoxazol-5-ones. The reaction of arylhydrazones of ethy cy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84520d585e4c85a2af3d34d0eeec7df2
https://doi.org/10.1007/bf00470286
https://doi.org/10.1007/bf00470286
Publikováno v:
Chemistry of Heterocyclic Compounds. 6:551-553
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d3f9ec9225bab8fb8b2590504e1795d
https://doi.org/10.1007/bf00500670
https://doi.org/10.1007/bf00500670