Synthesis of New Oxonine Series Macrolactones with Maphthopyrazine Fragments

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

The reaction of 3-[(amino-2-naphthyl)amino]-5,5-dimethylcyclohex-2-en-1-one with o-quinones provided previously unknown macrolactones of the oxonine series with naphthopyrazine fragments.

全文:

受限制的访问

作者简介

L. Ukhin

Institute of Physical and Organic Chemistry, Southern Federal University

编辑信件的主要联系方式.
Email: lyuhin@sfedu.ru
俄罗斯联邦, Rostov-on-Don

L. Kuzmina

N. S. Kurnakov Institute of General and Inorganic Chemistry of the Russian Academy of Sciences

Email: lyuhin@sfedu.ru
俄罗斯联邦, Moscow

V. Podshibyakin

Institute of Physical and Organic Chemistry, Southern Federal University

Email: lyuhin@sfedu.ru
俄罗斯联邦, Rostov-on-Don

L. Belousova

Institute of Physical and Organic Chemistry, Southern Federal University

Email: lyuhin@sfedu.ru
俄罗斯联邦, Rostov-on-Don

A. Morkovnik

Institute of Physical and Organic Chemistry, Southern Federal University

Email: lyuhin@sfedu.ru
ORCID iD: 0000-0002-9182-6101
俄罗斯联邦, Rostov-on-Don

E. Shepelenko

Southern Scientific Center of the Russian Academy of Sciences

Email: lyuhin@sfedu.ru
俄罗斯联邦, Rostov-on-Don

G. Borodkin

Institute of Physical and Organic Chemistry, Southern Federal University

Email: lyuhin@sfedu.ru
ORCID iD: 0000-0002-5886-7825
俄罗斯联邦, Rostov-on-Don

P. Chepurnoi

Institute of Physical and Organic Chemistry, Southern Federal University

Email: lyuhin@sfedu.ru
俄罗斯联邦, Rostov-on-Don

参考

  1. Ukhin L.Yu., Suponitsky K.Yu., Shepelenko E.N., Belousova L.V., Borodkin G.S. // Tetrahedron Lett. 2012. N 53. P. 67. doi: 10.1016/j.tetlet.2011.10.147
  2. Mancini I., Vigna J., Sighel D., Defant A. // Molecules. 2022. N 27. P. 4948. doi: 10.3390/molecules27154948
  3. Rahman Md M., Islam Md R., Akash S., Shohag S., Ahmed L., Supti F. A., Rauf A., Aljohani A.S.M., Abdulmonem W. Al, Khalil A.A., Sharma R., Thiruvengadam M. // Chem. Biol. Interact. 2022. Vol. 368. P. 110198. doi: 10.1016/j.cbi.2022.110198.
  4. Ortiz-Pérez E., Rivera G., Salas C.O., Zarate-Ramos J.J., Trofymchuk O.S., Hernandez-Soberanis L., Perales-Flores J.D., Vázquez K. // Curr. Top. Med. Chem. 2021. Vol. 21. P. 2046. doi: 10.2174/1568026621666210915121348
  5. Silva R.S.F., Pinto M.C.F.R., Goulart M.O.F., de Souza Filho J.D., Neves I., Jr., Lourenço M.C.S., Pinto A.V. // Eur. J. Med. Chem. 2009. Vol. 44. N 5. P. 2334. doi: 10.1016/j.ejmech.2008.06.014
  6. Makar S., Saha T., Singh S.K. // Eur. J. Med. Chem. 2019. Vol. 161. P. 252. doi: 10.1016/j.ejmech.2018.10.018
  7. Ukhin L.Yu., Kuz’mina L.G., Gribanova T.N., Borodkin G.S., Belousova L.V., Shepelenko E.N., Podshibyakin V.A., Chepurnoia P.B. // Mendeleev Commun. 2023. Vol. 33. P. 115. doi: 10.1016/j.mencom.2023.01.036
  8. Sousa E.T., da Silva M.M., de Andrade S.J., Cardoso M.P., Silva L.A., de Andrade J.B. // Thermochim. Acta. 2012. Vol. 529. P. 1. doi: 10.1016/j.tca.2011.11.012
  9. Beilstein. 1925. Vol. 7. P. 709.
  10. Siegmund W. // Monatsheft. 1908. Vol. 29. P. 1087. doi: 10.1007/BF01518745
  11. Abakumov G.A., Druzhkov N.O., Kurskii Y.A., Shavyrin A.S. // Russ. Chem. Bull. 2003. Vol. 52. P. 712. doi: 10.1023/A:1023979311368
  12. Dolomanov O.V., Bourhis L.J., Gildea R.J., Howard J.A.K., Puschmann H. // Appl. Cryst. 2009. Vol. 42. P. 339. doi: 10.1107/S0021889808042726
  13. Sheldrick G.M. // Acta Crystallogr. (A). 2015. Vol. 71. P. 3. doi: 10.1107/S2053273314026370
  14. Sheldrick G.M. // Acta Crystallogr. (A). 2015. Vol. 64. P. 122. doi: 10.1107/S0108767307043930

补充文件

附件文件
动作
1. JATS XML
2. Scheme 1

下载 (131KB)
3. Fig. 1. Molecular structure of compound 3a

下载 (254KB)
4. Scheme 2

下载 (98KB)
5. Fig. 2. Molecular structure of compound 3b

下载 (201KB)
6. Scheme 3

下载 (368KB)

版权所有 © Russian Academy of Sciences, 2024

##common.cookie##