Alkoxytelluration of Allylbenzene
- Авторы: Musalova M.V.1, Musalov M.V.1, Udalova S.I.1, Khabibulina A.G.1, Albanov A.I.1, Potapov V.A.1, Amosova S.V.1
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Учреждения:
- Favorskii Irkutsk Institute of Chemistry, Siberian Branch
- Выпуск: Том 54, № 4 (2018)
- Страницы: 526-529
- Раздел: Article
- URL: https://bakhtiniada.ru/1070-4280/article/view/217481
- DOI: https://doi.org/10.1134/S1070428018040024
- ID: 217481
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Аннотация
(2-Alkoxy-3-phenylpropyl)trichlorotellanes were synthesized by regioselective reaction of tellurium tetrachloride with allylbenzene in the system MeOH–CH2Cl2, as well as by nucleophilic substitution of chlorine in trichloro(2-chloro-3-phenylpropyl)tellane in MeOH–CH2Cl2 and EtOH–CHCl3. Allylbenzene reacted with tellurium tetrabromide on heating in methanol or ethanol. The reduction of (2-alkoxy-3-phenylpropyl) trihalotellanes with NaBH4 in H2O–THF gave 1,2-bis(2-alkoxy-3-phenylpropyl)ditellanes.
Об авторах
M. Musalova
Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Email: amosova@irioch.irk.ru
Россия, ul. Favorskogo 1, Irkutsk, 664033
M. Musalov
Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Email: amosova@irioch.irk.ru
Россия, ul. Favorskogo 1, Irkutsk, 664033
S. Udalova
Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Email: amosova@irioch.irk.ru
Россия, ul. Favorskogo 1, Irkutsk, 664033
A. Khabibulina
Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Email: amosova@irioch.irk.ru
Россия, ul. Favorskogo 1, Irkutsk, 664033
A. Albanov
Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Email: amosova@irioch.irk.ru
Россия, ul. Favorskogo 1, Irkutsk, 664033
V. Potapov
Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Email: amosova@irioch.irk.ru
Россия, ul. Favorskogo 1, Irkutsk, 664033
S. Amosova
Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Автор, ответственный за переписку.
Email: amosova@irioch.irk.ru
Россия, ul. Favorskogo 1, Irkutsk, 664033
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