Protolytic cleavage of derivatives of 2,5-dimethoxy-2,5-dihydrofuran

Authors

  • Д. Лоля Latvian Institute of Organic Synthesis, Riga LV-1006
  • Я. Фрейманис Latvian Institute of Organic Synthesis, Riga LV-1006
  • М. Гaвар Latvian Institute of Organic Synthesis, Riga LV-1006
  • Ю. Попелиc Latvian Institute of Organic Synthesis, Riga LV-1006
  • И. Typовский Latvian Institute of Organic Synthesis, Riga LV-1006
  • В. Беликов Latvian Institute of Organic Synthesis, Riga LV-1006

Abstract

By analysis of the products from the protolytic cleavage of methyl 3-(2,5-dialkoxy-2,5-dihydro-2-furyl)propionate (I) in the presence of mixed nucleophiles and investigation of their mutual transformations the main paths in the dissociation of the protonated molecule of (I), with the formation of both linear cleavage products (derivatives of 1,4-diketones and 4-ketopimelic acid) and furylcarbinol derivatives, were determined.

How to Cite
Lolya, D.; Freimanis, Y.; Gavar, M.; Popelis, Yu.; Turovskii, I.; Belikov, V. Chem. Heterocycl. Compd. 1997, 33, 164. [Khim. Geterotsikl. Soedin. 1997, 190.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF02256757

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Published

1997-02-25

Issue

No. 2 (1997)

Section

Original Papers