Reaction of Nitromethane with Phenylacetylene in Superbasic Media

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

Nitromethane reacts with phenylacetylene in the KOH(t-BuOK)/DMSO superbase media to form E- and Z-isomers of 4-benzyl-3-styryl-4,5-dihydroisoxazole-2-oxide, 2-benzyl-3-hydroxypropanonitrile and 1-benzyl-2-nitrocyclopropane.

作者简介

N. Lobanova

A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences

ORCID iD: 0000-0003-4594-1034
Irkutsk, Russia

I. Tatarinova

A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences

ORCID iD: 0000-0001-6237-8533
Irkutsk, Russia

I. Ushakov

A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences

ORCID iD: 0000-0003-0176-1699
Irkutsk, Russia

E. Schmidt

A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences

ORCID iD: 0000-0002-0188-3015
Irkutsk, Russia

B. Trofimov

A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences

Email: boris_trofimov@irioch.irk.ru
ORCID iD: 0000-0002-0430-3215
Irkutsk, Russia

参考

  1. Гареев Г.А., Свирская Л.Г. Химия нитрометана. Ред. Л.Б. Комарова. Новосибирск: Наука: Сибирская изд. фирма, 1995, 65–157.
  2. Злотни С.Г., Далингер И.Л., Махова Н.Н., Тартаковский В.А. Усп. хим. 2020, 89, 1–54.
  3. Aksenov N.A., Aksenov A.V., Ovcharov S.N., Aksenov D.A, Rubin M. Front. Chem. 2020, 77, 1–13. doi: 10.3389/fchem.2020.00077
  4. Проскуринина М.В., Шмидт Е.Ю., Васильцов А.М., Михалева А.М., Скорняков Ю.В., Трофимов Б.А., Зефиров Н.С. Жорж. 2003, 39, 291–292. doi: 10.1023/A:1025504722856
  5. Kukharov B.F., Stankevich V.K., Klimenko G.R. Mendeleev Commun. 2002, 2, 63–64. doi: 10.1002/chin.200239059
  6. Giacomelli G., Luca L.D., Porcheddu A. Tetrahedron. 2003, 59, 5437–5440. doi: 10.1016/S0040-4020(03)00859-7
  7. Basel Y., Hassner A. Synthesis. 1997, 309–312. doi: 10.1055/s-1997-1181
  8. Baglieri A., Meschisi L., Sarlo F.D., Machetti F. Eur. J. Org. Chem. 2016, 4643–4655. doi: 10.1002/ejoc.201600897
  9. Trofimov B.A., Schmidt E.Y., Zorina N.V., Ivanova E.V., Ilshakov.A. J. Org. Chem. 2012, 77, 6880–6886. doi: 10.1021/jo301005p
  10. Gotsko M.D., Sally I.V., Sobenina L.N., Ushakov I.A., Trofimov B.A. Tetrahedron Lett. 2019, 60, 151126–151130. doi: 10.1016/j.tetlet.2019.151126
  11. Sally I.V., Gotsko M.D., Sobenina L.N., Ushakov I.A., Trofimov B.A. Synthesis. 2020, 52, 2698–2704. doi: 10.1055/s-0040-1707148
  12. Sally I.V., Gotsko M.D., Sobenina L.N., Ushakov I.A., Trofimov B.A. Tetrahedron Lett. 2021, 84, 153432–153436. doi: 10.1016/j.tetlet.2021.153436
  13. Gotsko M.D., Sally I.V., Sobenina L.N., Ushakov I.A., Kireeva V.V., Trofimov B.A. Synthesis. 2022, 54, 1134–1144. doi: 10.1055/a-1681-4164
  14. Tomilin D.N., Sobenina L.N., Sally I.V., Ushakov I.A., Belogolova A.M., Trofimov B.A. New J. Chem. 2022, 46, 13149–13155. doi: 10.1039/D2NJ02011D
  15. Javad Kalbasi R., Mesgarsaravi N., Gharibi R. Appl. Organometal. Chem. 2019, 33, 4800–4819. doi: 10.1002/aoc.4800
  16. Lupidi G., Palmieri A., Petrini M. Adv. Synth. Catal. 2021, 363, 742–746. doi: 10.1002/adsc.202001344
  17. Feuer H. Nitrile Oxides, Nitrones, and Nitronates in Organic Synthesis, 2nd ed., New Jersey: Wiley, 2008, 1–129.

补充文件

附件文件
动作
1. JATS XML
下载

版权所有 © Russian Academy of Sciences, 2025