Interaction of 5-Hydroxypyrazolidine with Thiol-Containing Hydrazides as a Method of Synthesis of Biologically Active Ligands of Gold Glyco-Nanoparticles

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The interaction of (3S)-1-acetyl-5-hydroxy-2-phenyl-3-methylpyrazolidine with 6-mercaptohexanoic and 11-mercaptoundecanoic acid hydrazides leads to the formation in 60–65% yields of (3S)-1-acetyl-5-[(ω-mercaptoacyl)hydrazine]-2-phenyl-3-methylpyrazolidines as a promising сo-ligands for the production of gold glyco-nanoparticles for biomedical purposes.

作者简介

A. Ershov

Institute of Macromolecular Compounds of the Russian Academy of Sciences

Email: martynenkoff@gmail.com
ORCID iD: 0000-0002-2266-4380
俄罗斯联邦, Bol′shoi prosp., 31, St. Petersburg, 199004

A. Martynenkov

Institute of Macromolecular Compounds of the Russian Academy of Sciences

编辑信件的主要联系方式.
Email: martynenkoff@gmail.com
ORCID iD: 0000-0002-0951-1451
俄罗斯联邦, Bol′shoi prosp., 31, St. Petersburg, 199004

I. Lagoda

State Research Testing Institute of Military Medicine, Ministry of Defense of the Russian Federation

Email: martynenkoff@gmail.com
ORCID iD: 0000-0002-3906-2909
俄罗斯联邦, Lesoparkovaya ul., 4, St. Petersburg, 195043

A. Batyrenko

State Research Testing Institute of Military Medicine, Ministry of Defense of the Russian Federation

Email: martynenkoff@gmail.com
ORCID iD: 0000-0001-9688-3650
俄罗斯联邦, Lesoparkovaya ul., 4, St. Petersburg, 195043

参考

  1. Kutterer K.M.K., Davis J.M., Singh G., Yang Y., Hu W., Severin A., Rasmussen B.A., Krishnamurthy G., Failli A., Katz A.H. Bioorg. Med. Chem. Lett. 2005, 15, 2527–2531. doi: 10.1016/j.bmcl.2005.03.058
  2. Moydeen M., Kumar R.S., Idhayadhulla A., Manilal A. Mol. Divers. 2019, 23, 35–53. doi: 10.1007/s11030-018-9850-3
  3. Cheon H.G., Kim S.-S., Kim K.-R., Rhee S.-D., Yang S.D., Ahn J.H., Park S.-D., Lee J.M., Jung W.H., Lee H.S., Kim H.Y. Biochem. Pharm. 2005, 70, 22–29. doi: 10.1016/j.bcp.2005.04.004
  4. Naim M.J., Alam O., Nawaz F., Alam J., Alam P. J. Pharm. Bioallied Sci. 2016, 8, 2–17. doi: 10.4103/0975-7406.171694
  5. Wang W., Wang J., Ding Y. J. Mat. Chem. (B). 2020, 8, 4813–4830. doi: 10.1039/c9tb02924a
  6. Glycochemical synthesis: strategies and applications. Eds. S.-C. Hung, M.M.L. Zulueta. Hoboken, New Jersey: John Wiley & Sons Inc. 2016. doi: 10.1002/978 1119006435.ch16
  7. Ершов А.Ю., Мартыненков А.А., Лагода И.В., Копаница М.А., Зарубаев В.В., Слита А.В., Бучков Е.В., Панарин Е.Ф., Якиманский А.В. ЖОХ. 2021, 91, 1459–1464. [Ershov A.Y., Martynenkov A.A., Lagoda I.V., Kopanitsa M.A., Zarubaev V.V., Slita A.V., Buchkov E.V., Panarin E.F., Yakimansky A.V. Russ. J. Gen. Chem. 2021, 91, 1735–1739]. doi: 10.1134/S1070363221090 188
  8. Ершов А.Ю., Мартыненков А.А., Лагода И.В., Батыренко А.А., Драчев И.С., Якунчикова Е.А., Федорос Е.И., Круглов С.С., Копаница М.А., Якиманский А.В. ЖОХ. 2022, 92, 788–798. [Ershov A.Y., Martynenkov A.A., Lagoda I.V., Batyrenko A.A., Drachev I.S., Yakunchikova E.A., Fedoros E.I., Kruglov S.S., Kopanitsa M.A. Yakimansky A.V. Russ. J. Gen. Chem. 2022, 92, 850–859]. doi: 10.31857/S0044460X22050146
  9. Зеленин К.Н., Довгилевич А.В., Бежан И.П., Голубева Г.А., Свиридова Л.А., Пастушенков Л.В., Громова Е.Г., Гатчина Т.А., Помогайбо С.В. ХГС. 1984, 5, 659–666. [Zelenin K.N., Dovgilevich A.V., Bezhan I.P., Golubeva G.A., Sviridova L.A., Pastushenkov L.V., Gromova E.G., Gatchina T.A., Pomogaibo S.V. Chem. Heterocycl. Compd. 1984, 5, 529–536]. doi 10.1007/ BF00514307

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