Email this article Features of Reactions of Some 1-Arylaminomethylisatins with Girard’s Reagent T
- Authors: Bogdanov A.V.1, Gil’fanova A.R.1, Zaripova I.F.1, Mironov V.F.1
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Affiliations:
- Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Center
- Issue: Vol 88, No 1 (2018)
- Pages: 124-126
- Section: Letters to the Editor
- URL: https://journals.rcsi.science/1070-3632/article/view/221966
- DOI: https://doi.org/10.1134/S1070363218010206
- ID: 221966
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Abstract
Depending on the structure of the substituent at the endocyclic nitrogen atom, the reactions of aminomethylisatins with the Girard’s reagent T can proceed both with the elimination of the aminomethyl group and with its retention resulting in the formation of the corresponding positively charged isatin-3-acylhydrazones.
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About the authors
A. V. Bogdanov
Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Center
Author for correspondence.
Email: abogdanov@inbox.ru
Russian Federation, ul. Akademika Arbuzova 8, Kazan, Tatarstan, 420088
A. R. Gil’fanova
Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Center
Email: abogdanov@inbox.ru
Russian Federation, ul. Akademika Arbuzova 8, Kazan, Tatarstan, 420088
I. F. Zaripova
Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Center
Email: abogdanov@inbox.ru
Russian Federation, ul. Akademika Arbuzova 8, Kazan, Tatarstan, 420088
V. F. Mironov
Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Center
Email: abogdanov@inbox.ru
Russian Federation, ul. Akademika Arbuzova 8, Kazan, Tatarstan, 420088
