Abstract
The amination and hydroatnination of 5-alkyl-3H-furan-2-ones and their 3-benzylidene- and 3 formyl-derivatives were studied. The characteristics of the reactions, the requirements for the nature of the nucleophilic reagents, and the reaction conditions leading to the destruction of the furan ring and recyclization to pyrrolidinone and pyrrolinone structures are indicated.
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V. A. Sedavkina, N. A. Morozova, A. Ya. Egorova, and 1. G. Ostroumov, Khim. Geterotsikl. Soedin., No. 4, 451 (1987).
V. A. Sedavkina, N. A. Morozova, and A. Yu. Egorova, Khim. Geterotsikl. Soedin., No. 4, 456 (1993).
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 349–352, March, 1994.
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Morozova, N.A., Sedavkina, V.A. & Egorova, Y. Substitution of 3H-furan-2-ones in amination and hydroamination reactions. Chem Heterocycl Compd 30, 308–311 (1994). https://doi.org/10.1007/BF01165696
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DOI: https://doi.org/10.1007/BF01165696