Аннотация:
Reactions of 1-[(endo-bicyclo[3.3.1]non-6-en-3-yl)methyl]-3-tert-butylthiourea with I2/ButOOH and I2/K2CO3 afforded 4-azatricyclo[4.3.1.13,8]undecane based products via intramolecular cyclization, as determined by X-ray analysis and NMR spectroscopy.
Образец цитирования:
E. V. Nurieva, A. A. Alexeev, Yu. K. Grishin, V. A. Tafeenko, O. N. Zefirova, “New compounds with 4-azatricyclo[4.3.1.13,8]undecane framework”, Mendeleev Commun., 30:2 (2020), 145–146
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc1128
https://www.mathnet.ru/rus/mendc/v30/i2/p145
Эта публикация цитируется в следующих 3 статьяx:
Y. Sheena Mary, Y. Shyma Mary, Stevan Armaković, Sanja J. Armaković, Magdalena Pakosinska-Parys, Rohitash Yadav, Ismail Celik, “Investigation of reactive properties of an antiviral azatricyclo derivative–KDFT, MD and docking simulations”, Journal of Molecular Structure, 1230 (2021), 129937
Anna V. Evdokimova, Alexander A. Alexeev, Evgeniya V. Nurieva, Elena R. Milaeva, Sergei A. Kuznetsov, Olga N. Zefirova, “N-(4-Methoxyphenyl)-substituted bicyclic isothioureas: effect on morphology of cancer cells”, Mendeleev Communications, 31:3 (2021), 288
Evgeniya V. Nurieva, Alexander A. Alexeev, Olga N. Zefirova, “Cyclic Isothiourea in Drug Design”, Chem Heterocycl Comp, 57:9 (2021), 889
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