An effective approach to the synthesis of 2-([5ʹ-aryl-2,2ʹ-bipyridine]-6-yl)-5-aryl-1,3,4-oxadiazoles

Мұқаба

Дәйексөз келтіру

Толық мәтін

Аннотация

A convenient synthetic approach to derivatives of 2-(2,2ʹ-bipyridin-6-yl)-1,3,4-oxadiazoles is proposed as a result of the preparation using the “1,2,4-triazine” methodology of esters of 5-aryl-2,2ʹ-bipyridine-6-carboxylic acids and the subsequent construction of the 1,3,4-oxadiazole cycle by to modification of the ester group.

Авторлар туралы

M. Valieva

Ural Federal University named after the first President of Russia B.N. Yeltsin;Postovsky Institute of Organic Synthesis, UB, RAS

E. Starnovskaya

Ural Federal University named after the first President of Russia B.N. Yeltsin;Postovsky Institute of Organic Synthesis, UB, RAS

D. Kopchuk

Ural Federal University named after the first President of Russia B.N. Yeltsin;Postovsky Institute of Organic Synthesis, UB, RAS

E. Sharafieva

Ural Federal University named after the first President of Russia B.N. Yeltsin;Ural Medical University of the Ministry of Health of Russia

N. Slovesnova

Ural Federal University named after the first President of Russia B.N. Yeltsin;Postovsky Institute of Organic Synthesis, UB, RAS;Ural Medical University of the Ministry of Health of Russia

I. Kovalev

Ural Federal University named after the first President of Russia B.N. Yeltsin

E. Nosova

Ural Federal University named after the first President of Russia B.N. Yeltsin;Postovsky Institute of Organic Synthesis, UB, RAS

G. Zyryanov

Ural Federal University named after the first President of Russia B.N. Yeltsin;Postovsky Institute of Organic Synthesis, UB, RAS

Email: gvzyryanov@gmail.com

O. Chupakhin

Ural Federal University named after the first President of Russia B.N. Yeltsin;Postovsky Institute of Organic Synthesis, UB, RAS

Әдебиет тізімі

  1. Vaghani H., Patel S., Patel S. Int. J. Pharm. Sci. Res. 2021, 12, 5292-5299. doi: 10.13040/IJPSR.0975-8232.12(10).5292-99
  2. Luczynski M., Kudelko A. Appl. Sci. 2022, 12, 3756. doi: 10.3390/app12083756
  3. Johns B.A., Weatherhead J.G., Allen S.H., Thompson J.B., Garvey E.P., Foster S.A., Jeffrey J.L., Miller W.H. Bioorg. Med. Chem. Lett. 2009, 19, 1807-1810. doi: 10.1016/j.bmcl.2009.01.089
  4. Ravichandran V., Shalini S., Sundram K., Sokkalingam A.D. Eur. J. Med. Chem. 2010, 45, 2791-2797. doi: 10.1016/j.ejmech.2010.02.062
  5. Zeyuan D., Shuaiwei Q., Jing Z., Ze L., Chenyang Z. Пат. CN112125924В (2020). КНР. 2020, C07D519/00.
  6. Qi S., Zhang C., Yu H., Zhang J., Yan T., Lin Z., Yang B., Dong Z. J. Am. Chem. Soc. 2021, 143, 3284-3288. doi: 10.1021/jacs.0c12128
  7. Miki T., Nagaoka M., Hayashi S., Taniguchi Y., Ichikawa M. Пат. EP1746094A1 (2007). Яп. 2007, C07D413/14.
  8. Ichikawa M., Kawaguchi T., Kobayashi K., Miki T., Furukawa K., Koyama T., Taniguchi Y. J. Mater. Chem. 2006, 16, 221-225.
  9. Miki T., Yokoyama N., Hayashi S., Kusano S., Taniguchi Y., Ichikawa M. Пат. EP1932842A1 (2008). Яп. 2008, H01L51/007. doi: 10.1039/B510720B
  10. Yen F.-W., Chiu C.-Y., Lin I-F., Teng C.-M., Yen P.-C. Пат. US7282586B1 (2007). США. 2007, H01L51/007.
  11. Johns B.A., Weatherhead J.G., Allen S.H., Thompson J.B., Garvey E.P., Foster S.A., Jeffrey J.L., Miller W.H. Bioorg. Med. Chem. Lett. 2009, 19, 1807-1810. doi: 10.1016/j.bmcl.2009.01.090
  12. Dong Z., Qi S., Zhang J., Lin Z., Zhang C. Пат. CN112125924A (2020). Китай. 2020, C07D519/00.
  13. Ahuja S. Adv. Drug Deliv. Rev. 2007, 59, 3-11. doi: 10.1016/j.addr.2006.10.003
  14. Kopchuk D.S., Krinochkin A.P., Kozhevnikov D.N., Slepukhin P.A. Polyhedron. 2016, 118, 30-36. doi: 10.1016/j.mencom.2017.07.026
  15. Прохоров А.М., Кожевников Д.Н. ХГС. 2012, 8, 1237-1261.
  16. Prokhorov A.M., Kozhevnikov D.N. Chem. Heterocycl. Compd. 2012, 48, 1153-1176. doi: 10.1007/s10593-012-1117-9
  17. Foster R.A.A., Willis M.C. Chem. Soc. Rev. 2013, 42, 63-76. doi: 10.1039/C2CS35316D
  18. Luczynski M., Kudelko A. Appl. Sci. 2022, 12, 3756. doi: 10.3390/app12083756

Қосымша файлдар

Қосымша файлдар
Әрекет
1. JATS XML
Жүктеу

© Russian Academy of Sciences, 2023

Согласие на обработку персональных данных

 

Используя сайт https://journals.rcsi.science, я (далее – «Пользователь» или «Субъект персональных данных») даю согласие на обработку персональных данных на этом сайте (текст Согласия) и на обработку персональных данных с помощью сервиса «Яндекс.Метрика» (текст Согласия).