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Mendeleev Communications, 1997, Volume 7, Issue 4, Pages 139–141
DOI: https://doi.org/10.1070/MC1997v007n04ABEH000765
(Mi mendc4824)
 

This article is cited in 1 scientific paper (total 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
Full-text PDF (118 kB) Citations (1)
Abstract: Treatment of bicyclic monoterpene diketone with a modified carane skeleton with acylhydrazines results in stable N-acylpyrazolinols in 26–86% yield.
Document Type: Article
Language: English


Citation: S. A. Popov, A. V. Tkachev, “Synthesis of chiral N-acyl-2-pyrazolin-5-ols with a modified carane carbon frame”, Mendeleev Commun., 7:4 (1997), 139–141
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  • https://www.mathnet.ru/eng/mendc4824
  • https://www.mathnet.ru/eng/mendc/v7/i4/p139
  • This publication is cited in the following 1 articles:
    1. S. A. POPOV, A. V. TKACHEV, “ChemInform Abstract: Synthesis of Chiral N‐Acyl‐2‐pyrazolin‐5‐ols with a Modified Carane Carbon Frame.”, ChemInform, 28:49 (1997)  crossref
    Citing articles in Google Scholar: Russian citations, English citations
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