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

Journal

Mendeleev Communications
ISSN: 0959-9436

Output data

Year: 1997, Number: 4, Pages: 139-141 Pages count : 3 DOI: 10.1070/MC1997v007n04ABEH000765

Authors

Popov S.A. ¹ , Tkachev A.V. ¹

Affiliations

1	Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, 630090 Novosibirsk, Russian Federation

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

Popov S.A. , Tkachev A.V.
Synthesis of chiral N-acyl-2-pyrazolin-5-ols with a modified carane carbon frame
Mendeleev Communications. 1997. N4. P.139-141. DOI: 10.1070/MC1997v007n04ABEH000765 WOS Scopus РИНЦ OpenAlex

Published print:

Jan 1, 1997

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