Chemistry of Heterocyclic Compounds p. 662 - 667 (1981)
Update date:2022-08-22
Topics:
Shustov, G. V.
Tavakalyan, N.B.
Pleshkova, A. P.
Kostyanovskii, R. G.
The amidation and alkaline hydrolysis of diazirine-3,3-dicarboxylic acid esters, which proceed with retention of the diazirine ring, were studied.The higher stability of diazirine-3,3-dicarboxylic acid esters as compared with their spirocyclic analogs is explained by the conformational lability of the C=O groups.The UV and mass spectra of the diazirines are discussed.
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