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

封面

如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅存取

详细

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.

作者简介

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

参考

  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

补充文件

附件文件
动作
1. JATS XML
下载

版权所有 © Russian Academy of Sciences, 2023