Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Sergiy V. Kemskiy"'
Publikováno v:
Журнал органічної та фармацевтичної хімії, Vol 20, Iss 2, Pp 27-51 (2022)
Aim. To analyze and summarize the synthetic potential of 1,2,3-triazole-4(5)-amines as efficient building blocks in the synthesis of triazolo-annulated pyridine, azine and azepine systems. Results and discussion. Original literature sources revealin
Externí odkaz:
https://doaj.org/article/5633e45214624081941674431785b23c
Autor:
Alina N. Grozav, Sergiy V. Kemskiy, Mariana Z. Fedoriv, Vitaliy А. Chornous, Alina А. Palamar, Viktor I. Dorokhov, Eduard B. Rusanov, Mikhailo V. Vovk
Publikováno v:
Chemistry of Heterocyclic Compounds. 58:24-31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ead7c3e14ff7fa2ef52f8b0156e6e3ee
https://doi.org/10.1007/s10593-022-03052-3
https://doi.org/10.1007/s10593-022-03052-3
Autor:
Eduard B. Rusanov, M. V. Vovk, Vladislav M. Polishchuk, A. N. Grozav, Nikolay P. Shandura, Mariana Z. Fedoriv, Vitaliy А. Chornous, Sergiy V. Kemskiy
Publikováno v:
Chemistry of Heterocyclic Compounds. 57:1024-1030
5-Chloro-4-formylpyrrole-3-carboxylates react with anilines or β-naphthylamine when heated in DMF under reflux to form ethyl pyrrolo[2,3-b]quinoline-3-carboxylates or their benzo[f] analogs, which exhibit moderate fluorescent properties. The corresp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1782cc4edd425858e7840ed485ec57ec
https://doi.org/10.1007/s10593-021-03017-y
https://doi.org/10.1007/s10593-021-03017-y
Autor:
Natalia A. Syrota, A. V. Bol’but, Mykhailo V. Vovk, Igor I. Chernobaev, Oleksandr S. Liavinets, Sergiy V. Kemskiy
Publikováno v:
Chemistry of Heterocyclic Compounds. 57:841-847
4-(N-Boc-amino)-1Н-1,2,3-triazolecarbothioamides, obtained by a sequential treatment of 4-(N-Boc-amino)-1Н-1,2,3-triazoles with n-BuLi and alkyl isothiocyanates at –78÷–60°C, reacted with ethyl bromoacetate, forming the respective 4-(N-Boc-am
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::773c5c0614e984bada26948665d62179
https://doi.org/10.1007/s10593-021-02989-1
https://doi.org/10.1007/s10593-021-02989-1
Publikováno v:
Chemistry of Heterocyclic Compounds. 56:1048-1053
4-(N-Boc-amino)-1,2,3-triazole-5-carbaldehydes upon heating under reflux in acetic acid in the presence of pyrrolidine react with cycloalkanones, acetylacetone, 1,3-cyclohexanediones, and malononitrile resulting in annulation of the pyridine ring wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c4dfa9246e9e9438b2a9b61de922a97
https://doi.org/10.1007/s10593-020-02771-9
https://doi.org/10.1007/s10593-020-02771-9
Publikováno v:
Ukrainian Chemistry Journal. 86:100-110
The analysis of synthetic and biological importance of α-substituted β-prolines was conducted. Methods of synthesis of β-prolines and their esters, based on both intra- and intermolecular reactions of formation of functionalized pyrrolidinic cycle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f32d948d1d0c45f7ca5a46b0773295c4
https://doi.org/10.33609/0041-6045.86.2.2020.100-110
https://doi.org/10.33609/0041-6045.86.2.2020.100-110
Publikováno v:
Chemistry of Heterocyclic Compounds. 55:1092-1097
The corresponding ethyl 5-carbonylglycinates were synthesized by condensation of 4-(Boc-amino)-1,2,3-triazole-5-carboxylic acids with ethyl glycinate hydrochloride. They were intramolecularly cyclized with the selective formation of 1,4,6,7-tetrahydr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02b97df714a914da46ba50055f938864
https://doi.org/10.1007/s10593-019-02583-6
https://doi.org/10.1007/s10593-019-02583-6
Publikováno v:
Chemistry of Heterocyclic Compounds. 54:789-795
5-Amino-N-(2,2-dimethoxyethyl)-1Н-1,2,3-triazole-4-carboxamides in formic acid were subjected to intramolecular cyclization to 5-hydroxy[1,2,3]triazolo[4,5-е][1,4]diazepines, which were converted by treatment with S-nucleophiles to 5-thio-functiona
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::570b94e6bad662a5f0b2a16f30716fa4
https://doi.org/10.1007/s10593-018-2350-7
https://doi.org/10.1007/s10593-018-2350-7