1-chloroacetyloxindole(isatin) in reactions with some N-nucleophiles. Unexpetedly easy cleavage of chloroacetyl group
- Авторы: Bogdanov A.1, Kutuzova T.1, Krivolapov D.1, Dobrynin A.1, Mironov V.1
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Учреждения:
- Arbuzov Institute of Organic and Physical Chemistry
- Выпуск: Том 86, № 3 (2016)
- Страницы: 539-543
- Раздел: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/214172
- DOI: https://doi.org/10.1134/S1070363216030087
- ID: 214172
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Аннотация
Reactions of 1-chloroacetyloxindole and 1-chloroacetylisatin with some secondary amines, Girard’s reagent T and thiourea were studied. All investigated reactions proceeded via cleavage of the acyl group to form 3-substituted isatin or oxindole derivatives.
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Об авторах
A. Bogdanov
Arbuzov Institute of Organic and Physical Chemistry
Автор, ответственный за переписку.
Email: abogdanov@inbox.ru
Россия, ul. Akademika Arbuzova 8, Kazan, Tatarstan, 420088
T. Kutuzova
Arbuzov Institute of Organic and Physical Chemistry
Email: abogdanov@inbox.ru
Россия, ul. Akademika Arbuzova 8, Kazan, Tatarstan, 420088
D. Krivolapov
Arbuzov Institute of Organic and Physical Chemistry
Email: abogdanov@inbox.ru
Россия, ul. Akademika Arbuzova 8, Kazan, Tatarstan, 420088
A. Dobrynin
Arbuzov Institute of Organic and Physical Chemistry
Email: abogdanov@inbox.ru
Россия, ul. Akademika Arbuzova 8, Kazan, Tatarstan, 420088
V. Mironov
Arbuzov Institute of Organic and Physical Chemistry
Email: abogdanov@inbox.ru
Россия, ul. Akademika Arbuzova 8, Kazan, Tatarstan, 420088