Zobrazeno 1 - 10
of 45
pro vyhledávání: '"A. N. Esipenko"'
Autor:
O. I. Sizaya, V. N. Britsun, S. V. Gatsenko, V. N. Chelyabieva, O. L. Gumenyuk, A. N. Esipenko
Publikováno v:
Protection of Metals and Physical Chemistry of Surfaces. 46:71-74
Effect of the nature and position of substituents in [1,3]thiazino[3,2-a]benzimidazol-4-ones on their efficiency as corrosion inhibitors for steel 20 (HCl, pH 0) was studied.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60e5e1d56e069531c379088c3df76e05
https://doi.org/10.1134/s2070205110010107
https://doi.org/10.1134/s2070205110010107
Publikováno v:
Russian Journal of Organic Chemistry. 45:1834-1842
Reactions of ethyl 1-alkyl-5-benzoyl-6-methylsulfanyl-2-oxo-1,2-dihydropyridine-3-carboxylates with nitrogen-containing 1,4- and 1,5-binucleophiles (o-phenylenediamine, o-aminobenzenethiol, ethane-1,2-diamine, and propane-1,3-diamine) involved recycl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1545b1e71ca2854dc3f1de046c666850
https://doi.org/10.1134/s1070428009120148
https://doi.org/10.1134/s1070428009120148
Publikováno v:
Chemistry of Heterocyclic Compounds. 45:445-453
For the first time the possibility has been shown of recyclizing 1-alkyl-5-benzoyl-3-ethoxycarbonyl-6-methylthio-1,2-dihydropyridin-2-ones into 1,6-annelated bicyclic derivatives of 3-alkylcarbamoyl-5-benzoylpyridin-2-one, which takes place on reacti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2cf15d6b78bd6ee7f1d7a76bb2d54e8c
https://doi.org/10.1007/s10593-009-0284-9
https://doi.org/10.1007/s10593-009-0284-9
Publikováno v:
Chemistry of Heterocyclic Compounds. 44:1429-1459
Data from the last six years on the heterocyclization of thioamides containing an active methylene group are analyzed and classified.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::69ac89d496781d0b0b4da0f763515779
https://doi.org/10.1007/s10593-009-0214-x
https://doi.org/10.1007/s10593-009-0214-x
Publikováno v:
Chemistry of Heterocyclic Compounds. 44:979-984
[3+3] Cyclocondensation of 5-benzoyl-3-ethoxycarbonyl-6-methylthio-1-R-1,2-dihydropyrid-2-ones with heterocyclic N,N-and N,C-1,3-dinucleophiles proceeds regioselectively to give a series of new tri-and tetracyclic heterosystems, viz. derivatives of 5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::80ffaa21efd9f823128a420eacf5f236
https://doi.org/10.1007/s10593-008-0142-1
https://doi.org/10.1007/s10593-008-0142-1
Publikováno v:
Chemistry of Heterocyclic Compounds. 44:876-881
The reaction of 5-benzoyl-3-ethoxycarbonyl-6-methylthio-1-R-1,2-dihydropyridin-2-ones with the nitrogen-containing 1,4-dinucleophiles o-phenylenediamine, o-aminothiophenol, and ethylenediamine, proceeds as a recyclization, the products of which are d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::113ff8a576101f7d95fc9935a3df9f18
https://doi.org/10.1007/s10593-008-0124-3
https://doi.org/10.1007/s10593-008-0124-3
Synthesis and reactions of 1-R-3-benzoyl-5-ethoxycarbonyl-6-oxo-1,2,3,6-tetrahydropyridine-2-thiones
Publikováno v:
Chemistry of Heterocyclic Compounds. 43:1411-1419
Cycloacylation of N-R-3-oxo-3-phenylpropanethioamides by diethyl ethoxymethylenemalonate occurs selectively to form 1-R-3-benzoyl-5-ethoxycarbonyl-6-oxo-1,2,3,6-tetrahydropyridine-2-thiones which are convenient starting materials for the synthesis of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6f8ce7457e43fd83b2dec97d88f53351
https://doi.org/10.1007/s10593-007-0218-3
https://doi.org/10.1007/s10593-007-0218-3
Publikováno v:
Protection of Metals. 43:259-263
[1,3]Thiazino[3,2-a]benzoimidazol-4-ones were found to be effective inhibitors of the acid corrosion of steel 20 in 1 M HCl and 1 M H2SO4(pH 0) and valuable polyfunctional additives that enhance the anticorrosion properties and stimulate the formatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e4ae477a2223d6b37c4c66df29dd31f
https://doi.org/10.1134/s0033173207030095
https://doi.org/10.1134/s0033173207030095
Publikováno v:
Russian Journal of Organic Chemistry. 43:103-107
N-Aryl-3-oxobutanethioamides react with 2-amino-1,3-thiazole (2-amino-1,3-benzothiazole) in acetic acid to give mixtures of 7-methyl-5H-[1,3]thiazolo[3,2-a]pyrimidine-5-thione (2-methyl-4H-pyrimido-[2,1-b][1,3]benzothiazole-4-thione) and 5-arylimino-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e7ed39cbdfa4a435787f3c62786e8f6
https://doi.org/10.1134/s1070428007010137
https://doi.org/10.1134/s1070428007010137
Publikováno v:
Russian Journal of Organic Chemistry. 41:108-113
3-Aryl-1,2,4-triazole-5-thiones react with dimethyl acetylenedicarboxylate and methyl 3-phenyl-propynoate to afford the corresponding 5-substituted 2-aryl-7H-[1,2,4]triazolo[3,2-b][1,3]thiazin-7-ones. Treatment of 2-aryl-2,3-dihydro-4H-[1,3]thiazino[
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::874fad56b20d2961a6d9f8fea8505a1a
https://doi.org/10.1007/s11178-005-0130-1
https://doi.org/10.1007/s11178-005-0130-1