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.
Shustov, G. V.,Tavakalyan, N.B.,Pleshkova, A. P.,Kostyanovskii, R. G.
p. 662 - 667
(2007/10/02)
3,3-Diazirindicarbonsaeure ("Cyclodiazomalonsaeure") und einige ihrer Derivate
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Shustov, Gennady V.,Tavakalyan, Nina B.,Kostyanovsky, Remir G.
p. 206 - 207
(2007/10/02)
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