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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 1994 Volume 4, Issue 4, Pages 119–120 (Mi mendc5178)

This article is cited in 11 papers

Electrophilic 1,5-Addition of Acyl Chlorides to Conjugated Azocyclopropanes

Yu. V. Tomilov, G. P. Okonnishnikova, E. V. Shulishov, O. M. Nefedov

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation

Abstract: Addition reactions of acetyl and benzoyl chlorides to 1-pyrazolines containing a spiro cyclopropane fragment at the adjacent azo group lead selectively and in high yields to the corresponding 1-acyl-3-(chloroethyl)-2-pyrazolines, resulting in opening of the three-membered ring.

Language: English

DOI: 10.1070/MC1994v004n04ABEH000374



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