Substitution of 3H-furan-2-ones in amination and hydroamination reactions

Authors

  • Н. А. Морозова Scientific-Research Institute of Chemistry at Saratov State University, Saratov 410026
  • В. А. Седавкина Scientific-Research Institute of Chemistry at Saratov State University, Saratov 410026
  • А. Ю. Егорова Scientific-Research Institute of Chemistry at Saratov State University, Saratov 410026

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.

How to Cite
Morozova, N. A.; Sedavkina, V. A.; Egorova, A. Yu. Chem. Heterocycl. Compd. 1994, 30, 308. [Khim. Geterotsikl. Soedin. 1994, 349.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01165696

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Published

1994-03-25

Issue

No. 3 (1994)

Section

Original Papers