Key Blocks for Constructing π-Conjugated Systems Based on Thieno[3,2-b]pyrroles

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 订阅或者付费存取

详细

Cross-coupling products with isobutyl acrylate were obtained by the Heck reaction based on dibromides of methyl esters of 4-methyl- and 4-benzyl-4H-thieno[3,2-b]pyrrole-5-carboxylic acids.

全文:

受限制的访问

作者简介

S. Torosyan

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

Email: fangim@anrb.ru
ORCID iD: 0000-0002-9555-7228
俄罗斯联邦, Ufa, 450054

Z. Nuriakhmetova

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

Email: fangim@anrb.ru
ORCID iD: 0000-0002-7628-3452
俄罗斯联邦, Ufa, 450054

A. Lobov

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

Email: fangim@anrb.ru
ORCID iD: 0000-0002-9223-508X
俄罗斯联邦, Ufa, 450054

F. Gimalova

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

编辑信件的主要联系方式.
Email: fangim@anrb.ru
ORCID iD: 0000-0002-5176-1227
俄罗斯联邦, Ufa, 450054

参考

  1. Ching K.-Ch., Kam Y.-W., Merits A., Ng L.F.P., Chai C.L.L. // J. Med. Chem. 2015. Vol. 58. P. 9196. doi: 10.1021/acs.jmedchem.5b01047
  2. Hernando M.J.I., Ontoria J.M., Malancona S., Attenni B., Fiore F., Bonelli F., Koch U., Di Marco S., Colarusso S., Ponzi S., Gennari N., Vignetti S.E., Rico Ferreira M.d.R., Habermann J., Rowley M., Narjes F. // ChemMedChem. 2009. Vol. 4. N 10. P. 1695. doi: 10.1002/cmdc.200900184
  3. Jones C., Boudinet D., Xia Y., Denti M., Das A., Facchetti A. Driver T.G. // Chem. Eur. J. 2014. Vol. 20. N 20. P. 5938. doi: 10.1002/chem.201304914
  4. Gunawardhana R., Bulumulla C., Gamage P.L., Timmerman A.J., Udamulle Gedara C.M., Biewer M.C., Stefan M.C. // ACS Omega. 2019. Vol. 4. N 22. P. 19676. doi: 10.1021/acsomega.9b02274
  5. Arias A.C., MacKenzie J.D., McCulloch I., Rivnay J., Salleo A. // Chem. Rev. 2010. Vol. 110. P. 3. doi: 10.1021/cr900150b
  6. Gamage P.L., Udamulle Gedara C.M., Gunawardhana R., Bulumulla C., Ma Z., Shrivastava A., Biewer M.C., Stefan M.C. // Appl. Sci. 2022. Vol. 12. 3150. doi: 10.3390/app12063150
  7. Honsho Y., Saeki A., Seki Sh. // Int. J. Spectrosc. 2012. Vol. 2012. 983523. doi: 10.1155/2012/983523
  8. Beletskaya I.P., Cheprakov A.V. // Chem. Rev. 2000. Vol. 100. P. 3009. doi: 10.1021/cr9903048
  9. Biffis A., Centomo P., Del Zotto A., Zecca M. // Chem. Rev. 2018. Vol. 118. P. 2249. doi: 10.1021/acs.chemrev.7b00443
  10. Corbet J.P., Mignani G. // Chem. Rev. 2006. Vol. 106. P. 2651. doi: 10.1021/cr0505268
  11. Miftakhov M.S., Torosyan S.A., Gimalova F.A., Khursan S.L., Nuriakhmetova Z.F., Shchurik E.V., Kraevaya O.A., Shestakov A.F., Troshin P.A. // Polymer Chem. 2023. Vol. 14. P. 4986. doi: 10.1039/d3py00893b.
  12. Торосян С.А., Загитов В.В., Гималова Ф.А., Ерастов А.С., Мифтахов М.С. // ЖОрХ. 2018. Т. 54. С. 909; Torosyan S.A., Gimalova F.A., Zagitov V.V., Erastov A.S., Miftakhov M.S. // Russ. J. Org. Chem. 2018. Vol. 54. P. 912. doi: 10.1134/S1070428018060131
  13. Spencer A. // J. Organometal. Chem. 1984. Vol. 265. P. 323. doi: 10.1016/0022-328X(84)80097-2
  14. Stephan M.S., Teunissen A.J.J.M., Verzijl G.K.M., De Vries J.G. // Angew. Chem. Int. Ed. 1998. Vol. 37. P. 662. doi: 10.1002/(SICI)1521-3773(19980316)37:5<662::AID-ANIE662>3.0.CO;2-0

补充文件

附件文件
动作
1. JATS XML
下载
2. Scheme 1.

下载 (103KB)
索引源数据
3. Scheme 2.

下载 (98KB)
索引源数据
4. Scheme 3.

下载 (129KB)
索引源数据

版权所有 © Russian Academy of Sciences, 2024