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.
This is a preview of subscription content, log in via an institution to check access.
Similar content being viewed by others
References
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).
Author information
Authors and Affiliations
Additional information
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 349–352, March, 1994.
Rights and permissions
About this article
Cite this article
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
Issue Date:
DOI: https://doi.org/10.1007/BF01165696