Reaction of Nitromethane with Phenylacetylene in Superbasic Media

Мұқаба

Дәйексөз келтіру

Толық мәтін

Ашық рұқсат Ашық рұқсат
Рұқсат жабық Рұқсат берілді
Рұқсат жабық Рұқсат ақылы немесе тек жазылушылар үшін

Аннотация

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.

Авторлар туралы

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

Әдебиет тізімі

  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.

Қосымша файлдар

Қосымша файлдар
Әрекет
1. JATS XML
Жүктеу

© Russian Academy of Sciences, 2025