Аннотация:
(Z)-7-(3,5-Di-tert-butyl-6-oxocyclohexa-2,4-dien-1-ylidene)-1,3-dimethyl-3a,9a-diphenyl-1,3a,4,9a-tetrahydroimidazo[4,5-e]thiazolo[2,3-c][1,2,4]triazine-2,8(3H,7H)-dione was obtained by aldol condensation of 3,5-di-tert-butyl-1,2-benzoquinone with 1,3-dimethyl-3a,9a-diphenyl-3,3a,9,9a-tetrahydroimidazo[4,5-e]thiazolo[3,2-b][1,2,4]triazine-2,7(1H,6H)-dione followed by intramolecular thiazole ring-opening/closing in the condensation primary adduct.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
A. N. Kravchenko, G. A. Gazieva, S. V. Vasilevskii, Yu. V. Nelyubina, “Cascade synthesis of the first imidazo[4,5-e]-thiazolo[2,3-c][1,2,4]triazine derivative”, Mendeleev Commun., 24:2 (2014), 119–121
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc2493
https://www.mathnet.ru/rus/mendc/v24/i2/p119
Эта публикация цитируется в следующих 8 статьяx:
S.M. Ivanov, Comprehensive Heterocyclic Chemistry IV, 2022, 29
Н. Н. Махова, Л. И. Беленький, Г. А. Газиева, И. Л. Далингер, Л. С. Константинова, В. В. Кузнецов, А. Н. Кравченко, М. М. Краюшкин, О. А. Ракитин, А. М. Старосотников, Л. Л. Ферштат, С. А. Шевелев, В. З. Ширинян, В. Н. Яровенко, “Прогресс в химии азот-, кислород- и серасодержащих гетероциклических систем”, Усп. хим., 89:1 (2020), 55–124; N. N. Makhova, L. I. Belen'kii, G. A. Gazieva, I. L. Dalinger, L. S. Konstantinova, V. V. Kuznetsov, A. N. Kravchenko, M. M. Krayushkin, O. A. Rakitin, A. M. Starosotnikov, L. L. Fershtat, S. A. Shevelev, V. Z. Shirinian, V. N. Yarovenko, “Progress in the chemistry of nitrogen-, oxygen- and sulfur-containing heterocyclic systems”, Russian Chem. Reviews, 89:1 (2020), 55–124
Chita R. Sahoo, Sudhir K. Paidesetty, Rabindra N. Padhy, “Nornostocine congeners as potential anticancer drugs: An overview”, Drug Development Research, 80:7 (2019), 878
Galina A. Gazieva, Alexei N. Izmest'ev, Lada V. Anikina, Sergey A. Pukhov, Marina E. Meshchaneva, Dmitry V. Khakimov, Natalya G. Kolotyrkina, Angelina N. Kravchenko, “The influence of substituents on the reactivity and cytotoxicity of imidazothiazolotriazinones”, Mol Divers, 22:3 (2018), 585
Angelina N. Kravchenko, Sergei V. Vasilevskii, Galina A. Gazieva, Vladimir V. Baranov, Valery A. Barachevsky, Olga I. Kobeleva, Olga V. Venidiktova, Valentina A. Karnoukhova, “Transformations of S-substituted 5,7-dimethyl-4а,5а-diphenyl-3-thioxoperhydroimidazo[4,5-e]-1,2,4-triazin-2-ones under treatment of 1,2-benzoquinones and photochemical properties of reaction products”, Tetrahedron, 74:19 (2018), 2359
Galina A. Gazieva, Alexei N. Izmest'ev, Yulia V. Nelyubina, Natalya G. Kolotyrkina, Igor E. Zanin, Angelina N. Kravchenko, “Synthesis of imidazo[4,5-e]thiazolo[2,3-c]-1,2,4-triazine-2,8-diones via a rearrangement of imidazo[4,5-e]thiazolo[3,2-b]-1,2,4-triazine-2,7-diones in the reaction with isatins”, RSC Adv., 5:55 (2015), 43990
A. N. Kravchenko, S. V. Vasilevskii, G. A. Gazieva, Yu. V. Nelyubina, “Unexpected formation of 6-[benzofuran-3(2H)-ylidene]-3,3a,9,9a-tetra-hydroimidazo[4,5-e]thiazolo[3,2-b][1,2,4]triazine-2,7-dione derivative”, Mendeleev Commun., 25:6 (2015), 476–478
Angelina N. Kravchenko, Galina A. Gazieva, Sergei V. Vasilevskii, Yulia V. Nelyubina, “ChemInform Abstract: Cascade Synthesis of the First Imidazo[4,5‐e]thiazolo[2,3‐c][1,2,4]triazine Derivative (IV).”, ChemInform, 45:37 (2014)
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