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Abstract
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 analysis. The mechanism of solvolysis of triazolines (I) is discussed, along with the structural characteristics and stabilization factors of the O-tosylhydroxylamine products (II).
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Schedule a callMore From: Bulletin of the Academy of Sciences of the USSR Division of Chemical Science
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