Email this article Selective monoallylation of β-cyclodextrin
- Authors: Novokshonov V.V.1, Hoi N.C.2, Shaglaeva N.S.2
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Affiliations:
- Favorskii Irkutsk Institute of Chemistry, Siberian Branch
- Irkutsk National Research Technical University
- Issue: Vol 87, No 6 (2017)
- Pages: 1172-1174
- Section: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/220177
- DOI: https://doi.org/10.1134/S1070363217060111
- ID: 220177
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Abstract
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.
Keywords
About the authors
V. V. Novokshonov
Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Email: ShaglaevaNS@yandex.ru
Russian Federation, ul. Favorskogo 1, Irkutsk, 664033
Nguen Chyong Hoi
Irkutsk National Research Technical University
Email: ShaglaevaNS@yandex.ru
Russian Federation, ul. Lermontova 83, Irkutsk, 664074
N. S. Shaglaeva
Irkutsk National Research Technical University
Author for correspondence.
Email: ShaglaevaNS@yandex.ru
Russian Federation, ul. Lermontova 83, Irkutsk, 664074
