1-chloroacetyloxindole(isatin) in reactions with some  N -nucleophiles. Unexpetedly easy cleavage of chloroacetyl group

A. V. Bogdanov; T. A. Kutuzova; D. B. Krivolapov; A. B. Dobrynin; V. F. Mironov

doi:10.1134/S1070363216030087

1-chloroacetyloxindole(isatin) in reactions with some N-nucleophiles. Unexpetedly easy cleavage of chloroacetyl group

作者: Bogdanov A.¹, Kutuzova T.¹, Krivolapov D.¹, Dobrynin A.¹, Mironov V.¹
隶属关系:
1. Arbuzov Institute of Organic and Physical Chemistry
期: 卷 86, 编号 3 (2016)
页面: 539-543
栏目: Article
URL: https://journals.rcsi.science/1070-3632/article/view/214172
DOI: https://doi.org/10.1134/S1070363216030087
ID: 214172

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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.