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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 1997 Volume 7, Issue 4, Pages 139–141 (Mi mendc4824)

This article is cited in 1 paper

Synthesis of chiral N-acyl-2-pyrazolin-5-ols with a modified carane carbon frame

S. A. Popova, A. V. Tkachevb

a Department of Natural Sciences, Novosibirsk State University, Novosibirsk, Russian Federation
b N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation

Abstract: Treatment of bicyclic monoterpene diketone with a modified carane skeleton with acylhydrazines results in stable N-acylpyrazolinols in 26–86% yield.

Language: English

DOI: 10.1070/MC1997v007n04ABEH000765



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