C- or N- functionalization of tropilia salt 2-amino-4-methylthiazole or 5-aminotetrazole

Capa

Citar

Texto integral

Acesso aberto Acesso aberto
Acesso é fechado Acesso está concedido
Acesso é fechado Somente assinantes

Resumo

The charges on the reaction centers of 2-amino-4-methylthiazole and 5-aminotetrazole, which predetermine their interaction with tropylium tetrafluoroborate, were determined by quantum chemical calculation (AM1) in accordance with the charge control of the process. New compounds 4-methyl-5-(cyclohepta-11,31,51-trienyl)-2-aminothiazole and 5-( N , N -dicyclohepta-11,31,51-trienyl)aminotetrazole were obtained.

Sobre autores

L. Yunnikova

Perm State Agro-Technological University Named after Academician D.N. Pryanishnikov

Email: yunnikova@yahoo.com

T. Akent'eva

Perm State Agro-Technological University Named after Academician D.N. Pryanishnikov

E. Yunnikova

Perm State Agro-Technological University Named after Academician D.N. Pryanishnikov

Bibliografia

  1. Юнникова Л.П., Неустроев Д.А. ЖОрХ. 2022, 58, 227-234.
  2. Yunnikova L.P., Neustroev D.A. Russ. J. Org. Chem. 2022, 58, 227-234. doi: 10.31857/S0514749222030016
  3. Юнникова Л.П., Акентьева Т.А., Эсенбаева В.В. Хим.-фарм. ж. 2015, 49, 33-35. doi: 10.1007/s11094-015-1263-3
  4. Юнникова Л.П., Акентьева Т.А. Пат. РФ 2479571 (2013); Б.И., № 11.
  5. Юнникова Л.П., Лихарева Ю.А., Акентьева Т.А. ЖОХ. 2017, 87, 333-335.
  6. Yunnikova L.P., Likhareva Y.E., Akent'eva T.A. Russ. J. Gen. Chem. 2017, 87, 347-349. doi: 10.1134/S1070363217020323
  7. Королева Е.В., Гусак К.Н., Игнатович Ж.В. Усп. хим. 2010, 79, 720-745.
  8. Koroleva E.V., Gusak K.N., Ignatovich Zh.V. Russ. Chem. Rev. 2010, 79, 655-681. doi: 10.1070/RC2010v079n08ABEH004116
  9. Юнникова Л.П., Эсенбаева В.В., Шкляева Е.В. Изв. вузов. Хим. и хим. технол. 2018, 61, 47-52. doi: 10.6060/ivkkt.20186108.5817
  10. Салькеева Л.К., Нурмагенбетова Т.М, Минаева Е.В. ЖОХ. 2005, 75, 2065-2066.
  11. Sal'keeva L.K., Nurmagambetova M.T., Minaeva E.V. Russ. J. Gen. Chem. 2005, 75, 1975. doi: 10.1007/s11176-006-0027-x
  12. Попова Е.А., Трифонов Р. Е., Островский В.А. Усп. хим. 2019, 88, 644-676. doi: 10.1070/RCR 4864
  13. CrysAlisPro, Agilent Technologies, Version 1.171.37.33 (release 27-03-2014 CrysAlis171.NET)
  14. Sheldrick G.M. Acta Crystallogr., Sect. A. 2008, 64, 112-122. doi: 10.1107/S0108767307043930
  15. Sheldrick G.M. Acta Crystallogr., Sect. C. 2015, 71, 3-8. doi: 10.1107/S2053229614024218
  16. Dolomanov O.V., Bourhis L.J., Gildea R.J., Howard J.A.K., Puschmann H. J. Appl. Crystallogr. 2009, 42, 339-341. doi: 10.1107/S0021889808042726

Arquivos suplementares

Arquivos suplementares
Ação
1. JATS XML
Baixar

Declaração de direitos autorais © Russian Academy of Sciences, 2023