90713-16-9Relevant academic research and scientific papers
GEMINAL SYSTEMS. 50. SOLVOLYSIS OF 1-TOSYLOXY-Δ2-1,2,3-TRIAZOLINE-5,5-DICARBOXYLATE ESTERS AND THE STRUCTURE OF THE SOLVOLYSIS PRODUCT, O-TOSYL-N-α,α-BIS(ETHOXYCARBONYL)-β-METHOXYETHYLHYDROXYLAMINE
Shustov, G. V.,Zolotoi, A. B.,Belov, P. N.,Konovalikhin, S. V.,Atovmyan, L. O.,et al.
, p. 1651 - 1657 (2007/10/02)
Solvolysis of 1-tosyloxy-Δ2-1,2,3-triazoline-5,5-dicarboxylic acid esters (1) occurs via elimination of N2 and leads predominantly to N-β-hydroxylethyl-O-tosylhydroxylamines (II), whose structure was determined unequivocally by x-ray structural
1-ACYLOXYAZIRIDINE-2,2-DICARBOXYLIC ACID ESTERS
Mishchenko, A. I.,Prosyanik, V. A.,Belov, P. N.,Romanchenko, V. A.,Belova, E. G.,Markov, V. I.
, p. 270 - 274 (2007/10/02)
The reaction of diazomethane and O-acylisonitrosomalonates gave Δ2-1,2,3-triazoline-5,5-dicarboxylic acid esters, the rates of formation and thermal stabilities of which are determined by the character of this substituent attached to the oxygen
