Study of reaction of (E)-(3-aryl-3-oxoprop-1-en-1-yl)triphenylphosphonium bromides with 2-aminopyridine

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

(E)-(3-Aryl-3-oxoprop-1-en-1-yl)triphenylphosphoniumbromides react with 2-aminopyridine to form [(2-aryl-3-imidazo-[1,2-α-]pyridin-3-yl)methyl]triphenylphosphoniumbromides. An alternative scheme of the reactions is proposed, including an initial attack of the nucleophile on the carbonyl group.

全文:

受限制的访问

作者简介

R. Khachikyan

Institute of Organic Chemistry, Scientific and Technological Center of Organic and Pharmaceutical Chemistry, National Academy of Sciences of Armenia

编辑信件的主要联系方式.
Email: khachikyanraya@gmail.com
ORCID iD: 0009-0006-2014-7861
亚美尼亚, prosp. Azatutyan, 26, Yerevan, 0014

K. Harutyunyan

Institute of Organic Chemistry, Scientific and Technological Center of Organic and Pharmaceutical Chemistry, National Academy of Sciences of Armenia

Email: khachikyanraya@gmail.com
ORCID iD: 0000-0002-3274-1239
亚美尼亚, prosp. Azatutyan, 26, Yerevan, 0014

A. Ayvazyan

Institute of Organic Chemistry, Scientific and Technological Center of Organic and Pharmaceutical Chemistry, National Academy of Sciences of Armenia

Email: khachikyanraya@gmail.com
ORCID iD: 0000-0002-3224-0549
亚美尼亚, prosp. Azatutyan, 26, Yerevan, 0014

Z. Hovakimyan

Institute of Organic Chemistry, Scientific and Technological Center of Organic and Pharmaceutical Chemistry, National Academy of Sciences of Armenia

Email: khachikyanraya@gmail.com
ORCID iD: 0009-0000-1604-5834
俄罗斯联邦, prosp. Azatutyan, 26, Yerevan, 0014

参考

  1. Хачикян Р.Дж., Овакимян З.Г., Паносян Г.А., Тамазян Р.А., Айвазян А.Г. ЖОХ, 2017, 87, 1110–1116. doi: 10.1134/S1070363217070 106
  2. Хачикян Р.Дж., Овакимян З.Г., Карамян Э.О., Паносян Г.А. ЖОХ, 2019, 89, 218–222. doi: 10.1134/S1070363219020087
  3. Zbiral E. Tetrahedron Lett., 1970, 58, 5107–5110. doi: 10.1016/S0040-4039(00)96998-3
  4. Roth M., Dubs P., Gotschi E., Eschenmoser A. Helv. Chim. Acta., 1971, 54, 710–734. doi: 10.1002/hlca.19710540229
  5. Хачикян Р.Дж., Овакимян З.Г., Карамян Э.О., Балян А.А., Паносян Г.А. Хим. ж. Армении, 2021, 74, 154–160.
  6. Zbiral E., Bauer E. Tetrahedron, 1972, 28, 4189–4196. doi: 10.1016/S0040-4020(01)93649-x
  7. Zbiral E., Drescher M. Syntesis, 1988, 9, 735–739. doi: 10.1055/S-1988-27693
  8. Мегера И.В., Лебедев Л.Б., Шевчук М.И. ЖОХ, 1981, 51, 54–57.
  9. Townsend L.B. and. Shram K.H. Tetrahedron Lett., 1974, 1345–1348. doi: 10.1016/S0040-4039(01)82484-9
  10. Hugl E., Schulz G. and Zbiral E. Liebigs Ann. Chem, 1973, 278–289. doi: 10.1002/jlac.197319730216
  11. Хачикян Р.Дж., Овакимян З.Г., Паносян Г.А., Тамазян Р.А., Айвазян А.Г. ЖОХ, 2014, 84, 453–456. doi: 10.1134/S1070363214030177
  12. North A.C.T., Phillips D.C., Mathews F.S. Acta Crystallogr. (A), 1968, 24, 351–359. doi: 10.1107/S0567739468000707
  13. Sheldrick G.M. Acta Crystallogr., 2015, 71, 3–8. doi: 10.1107/S2053229614024218

补充文件

附件文件
动作
1. JATS XML
2. Scheme

下载 (233KB)
3. Figure. Molecular structure of compound 2c according to X-ray diffraction data. Anisotropic thermal ellipsoids are shown with 50% probability.

下载 (451KB)
4. Figure

下载 (184KB)

版权所有 © Russian Academy of Sciences, 2025