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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 1997 Volume 7, Issue 2, Pages 56–58 (Mi mendc4780)

This article is cited in 2 papers

Unusual reaction of aziridine dimer with acetylene dicarboxylates

R. G. Kostyanovskya, Yu. I. El'natanova, I. I. Chervina, M. Yu. Antipinb, A. V. Ivanovc

a N.N. Semenov Federal Research Center for Chemical Physics, Russian Academy of Sciences, Moscow, Russian Federation
b A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation
c A.N. Kosygin Moscow State Textile Academy, Moscow, Russian Federation

Abstract: The 1-(2-aminoethyl)aziridine (aziridine dimer) 1 reacts with acetylene dicarboxylates to give 1,4-diaza- 5-oxobicyclo[4.3.0]nonanes (7-azaindolizines) 3 together with the usual enamine adducts 4; the product structures are confirmed spectroscopically and, in the 3 also by X-ray diffraction and by an independent synthesis from furan 5.

Language: English

DOI: 10.1070/MC1997v007n02ABEH000708



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