Abstract:
A new method of dihydrothiadiazine cycle annelation to 1,2,4-triazole derivatives is suggested and a ring opening reaction of the obtained dihydrothiadiazine cycle is found, leading to a substituted desoxybenzoine; the structures of both reaction products are supported by X-ray analysis.
Citation:
A. A. Kolodina, A. V. Lesin, Yu. V. Nelyubina, “Ring formation and ring opening reactions of a dihydrothiadiazine cycle fused to 1,2,4-triazole”, Mendeleev Commun., 18:5 (2008), 253–254
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https://www.mathnet.ru/eng/mendc3316
https://www.mathnet.ru/eng/mendc/v18/i5/p253
This publication is cited in the following 11 articles:
Evgeniya Khodykina, Diana Pobedinskaya, Inna Borodkina, Alexander Astakhov, Oleg Demidov, Anatoly Metelitsa, Victor Chernyshev, Alexandra Kolodina, “A facile approach to the synthesis of 3,4-dihydro-2
H
-benzo[4,5]imidazo[2,1-b][1,3,4]thiadiazines”, Journal of Sulfur Chemistry, 45:6 (2024), 917
Evgenia S. Khodykina, Dmitry V. Steglenko, Elena V. Vetrova, Artem D. Pugachev, Maria S. Galkina, Inna G. Borodkina, Alexander V. Lesin, Oleg P. Demidov, Anatoly V. Metelitsa, Alexandra A. Kolodina, “Intramolecular Cyclization of the ortho‐Substituted N‐arylquinone Imines under Basic and Thermal Conditions”, ChemistrySelect, 8:3 (2023)
A. A. Kolodina, D. V. Steglenko, E. S. Khodykina, N. I. Gaponenko, M. S. Galkina, O. P. Demidov, A. V. Metelitsa, “Unusual cyclization of N-imidazolyl quinone imines with the formation of thiadiazole ring and its subsequent recyclization”, Mendeleev Commun., 32:3 (2022), 386–389
Alexandra A. Kolodina, Arshak A. Tsaturyan, Maria S. Galkina, Inna G. Borodkina, Elena V. Vetrova, Oleg P. Demidov, Alexandra G. Berezhnaya, Anatoly V. Metelitsa, “6,7‐Dihydro‐5H‐1,2,4‐triazolo[3,4‐b][1,3,4]thiadiazine Ring Cleavage and Tautomerism of the Products: Experimental and Theoretical Study”, ChemistrySelect, 5:12 (2020), 3586
Konstantin L'vovich Obydennov, Tatiana Andreevna Kalinina, Olga Alexandrovna Vysokova, Pavel Alexandrovich Slepukhin, Varvara Alexandrovna Pozdina, Maria Valer'evna Ulitko, Tatiana Vladimirovna Glukhareva, “The different modes of chiral [1,2,3]triazolo[5,1-b][1,3,4]thiadiazines: crystal packing, conformation investigation and cellular activity”, Acta Crystallogr C Struct Chem, 76:8 (2020), 795
D. I. Bugaenko, A. V. Karchava, M. A. Yurovskaya, “Synthesis of indoles: recent advances”, Russian Chem. Reviews, 88:2 (2019), 99–159
Bakr F. Abdel-Wahab, Ismail Althagafi, “Recent Progress in the Synthetic Routes to Triazolothiadiazines”, Phosphorus, Sulfur, and Silicon and the Related Elements, 189:10 (2014), 1433
N. I. Gaponenko, A. A. Kolodina, A. V. Lesin, S. V. Kurbatov, “Intramolecular cyclization of S-alkyl derivatives of aminomercaptoimidazoles and -benzimidazoles as a method for the annulation of the thiadiazine ring”, Russ Chem Bull, 61:6 (2012), 1154
O. V. Serdyuk, V. T. Abaev, A. A. Kolodina, A. V. Butin, “First example of the synthesis of indoles on a heterocyclic matrix”, Chem Heterocycl Comp, 47:3 (2011), 381
N. I. Gaponenko, A. A. Kolodina, A. V. Lesin, S. V. Kurbatov, Z. A. Starikova, Yu. V. Nelyubina, “Synthesis of spiro[indole-3,3′-[1,3,4]thiadiazino[3,2-a]benzimidazoles] and spiro[indole-3,6′-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazines]”, Russ Chem Bull, 59:4 (2010), 838
Alexandra A. Kolodina, Alexandr V. Lesin, Yulia V. Nelyubina, “ChemInform Abstract: Ring Formation and Ring Opening Reactions of a Dihydrothiadiazine Cycle Fused to 1,2,4‐Triazole.”, ChemInform, 40:13 (2009)
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