Selective monoallylation of β-cyclodextrin
- Авторы: Novokshonov V.1, Hoi N.2, Shaglaeva N.2
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Учреждения:
- Favorskii Irkutsk Institute of Chemistry, Siberian Branch
- Irkutsk National Research Technical University
- Выпуск: Том 87, № 6 (2017)
- Страницы: 1172-1174
- Раздел: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/220177
- DOI: https://doi.org/10.1134/S1070363217060111
- ID: 220177
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Аннотация
Reaction of β-cyclodextrin with allyl bromide in dimethyl sulfoxide affords 2-О-allyl-β-cyclodextrin, while in dimethylformamide 6-О-allyl-β-cyclodextrin is formed. Optimal conditions of the reaction were found allowing to obtain the target products in quantitative yield.
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Об авторах
V. Novokshonov
Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Email: ShaglaevaNS@yandex.ru
Россия, ul. Favorskogo 1, Irkutsk, 664033
Nguen Hoi
Irkutsk National Research Technical University
Email: ShaglaevaNS@yandex.ru
Россия, ul. Lermontova 83, Irkutsk, 664074
N. Shaglaeva
Irkutsk National Research Technical University
Автор, ответственный за переписку.
Email: ShaglaevaNS@yandex.ru
Россия, ul. Lermontova 83, Irkutsk, 664074