New cross-conjugiated chlorocyclopentenone derivatives containing amino acids fragments at C-3

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Abstract

The reaction of 5-allenyl-2,3,5-trichlorocyclopentenone with methyl esters of glycine, L-methionine, L-leucine and L-tyrosine produced the corresponding AdNE adducts, the oxidative cleavage of the allene fragment of which produced new 4-carboxymethylidene derivatives.

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About the authors

L. S. Khasanova

Ufa Institute of Chemistry, Ufa Federal Research Center of the Russian Academy of Sciences

Email: fangim@anrb.ru
ORCID iD: 0000-0002-7183-4200
Russian Federation, Ufa, 450054

V. A. Egorov

Ufa Institute of Chemistry, Ufa Federal Research Center of the Russian Academy of Sciences

Email: fangim@anrb.ru
ORCID iD: 0000-0001-9710-265X
Russian Federation, Ufa, 450054

M. F. Abdullin

Ufa Institute of Chemistry, Ufa Federal Research Center of the Russian Academy of Sciences

Email: fangim@anrb.ru
ORCID iD: 0000-0002-9894-213X
Russian Federation, Ufa, 450054

F. A. Gimalova

Ufa Institute of Chemistry, Ufa Federal Research Center of the Russian Academy of Sciences

Author for correspondence.
Email: fangim@anrb.ru
ORCID iD: 0000-0002-5176-1227
Russian Federation, Ufa, 450054

References

  1. Monto A.S. Clin. Infect. Dis., 2008, 47, 346–348. doi: 10.1086/589749
  2. Ахметвалеев Р.Р., Акбутина Ф.А., Иванова Н.А., Мифтахов М.С. Изв. АН. Сер. хим. 2001, 1417–1435. [Akhmetvaleev R.R., Akbutina F.A., Ivanova N.A., Miftakhov M.S. Russ. Chem. Bull., Int. Ed. 2001, 50, 1489–1509.]doi: 10.1023/A:1013038427455
  3. Акбутина Ф.А., Торосян С.А., Мифтахов М.С. Изв. АН. Сер. хим. 1997, 1646–1648. [Akbutina F.A., Torosyan S.A., Miftakhov M.S. Russ. Chem. Bull., Int. Ed. 1997, 46, 1569–1571.] doi: 10.1007/BF02502941
  4. Гилязетдинов Ш.Я., Юсупова З.Ф., Саитова М.Ю., Зарудий Ф.С., Ахметвалеев Р.Р., Мифтахов М.С., Акбутина Ф.А., Торосян С.А. Пат. 2144767 (1997). РФ. Б.И. 2000, № 3.
  5. Гималова Ф.А., Егоров В.А., Торосян С.А., Мифтахов М.С. ЖОрХ. 2007, 43 (7), 987–989. [Gimalova F.A., Egorov V.A., Torosyan S.A., Miftakhov M.S. Russ. J. Org. Chem. 2007, 43, 981–983.] doi: 10.1134/S1070428007070068.
  6. Егоров В.А., Гималова Ф.А., Хасанова Л.С., Мифта-хов М.С. ЖОрХ. 2015, 51 (12), 1755–1758. [Egorov V.A., Khasanova L.S., Gimalova F.A., Miftakhov M.S. Russ. J. Org. Chem. 2015, 51, 1721–1724.] doi: 10.1134/S107042801512009X
  7. Гималова Ф.А., Егоров В.А., Мифтахов М.С., Еримбетов К.Т., Подгородниченко В.К. Пат. 2599792 (2015). РФ. Б.И. 2016, № 29.
  8. Хейнс А. Методы окисления органических соединений. М: Мир, 1988, 163–164. [Haines A.H., Metody okisleniya organicheskikh soedineniy (Methods for the Oxidation of Organic Compounds), Moscow: Mir, 1988, 163–164].
  9. Чертанова Л.И., Акбутина Ф.А., Торосян С.А., Халилов Л.М., Мифтахов М.С. Изв. АН. Сер. хим. 1997, 1979–1981 [Chertanova L.F., Akbutina F.A., Torosyan S.A., Khalilov L.M., Miftakhov M.S. Russ. Chem. Bull., 1997, 46, 1875–1877.] doi: 10.1007/BF02503776

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