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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. Popov
a
,
A. V. Tkachev
b
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
Fulltext:
PDF file (118 kB)
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Steklov Math. Inst. of RAS
, 2025