UNUSUAL AMINO ACIDS. 5. SYNTHESIS OF 3,5-DIOXOPYRAZOLIDINE DERIVATIVES

Authors

  • Д. Р. Зицане Riga Technical University
  • З. Ф. Тетере Riga Technical University
  • И. А. Рийкуре Riga Technical University
  • М. В. Петрова Riga Technical University
  • Э. Ю. Гудриниеце Riga Technical University
  • У. О. Калей BAPEKS

DOI:

https://doi.org/10.1007/261

Keywords:

3, 5-dioxopyrazolidines, malonic acid, monohydrazides of 2-R-4-methyl-4-cyclohexene-1, 1-dicarboxylic acids

Abstract

Monohydrazides of 2-R-4-methyl-4-cyclohexene-1,1-dicarboxylic acids react with trifluoroacetic acid anhydride to give 4-substituted 3,5-dioxopyrazolidines, with phosphorus trichloride to give 4‑(2‑R‑5‑chloro-4‑methylcyclohexane)-3,5-dioxopyrazolidines, and with acetic anhydride to give 4‑(2‑R‑4-methyl-4-cyclohexene)-3,5-diacetoxypryazoles.

Authors: D. Zicane, Z. Tetere, I. Rijkure, M. V. Petrova, E. Gudriniece, and U. Kalejs.

English Translation in Chemistry of Heterocyclic Compounds, 2000, 36 (7), pp 792-795

http://link.springer.com/article/10.1007/BF02256911

Published

2013-02-06

Issue

Section

Original Papers