M. Janik et V. Machacek, KINETICS OF CYCLIZATION OF METHYL-S-(2,6-DINITRO-4-METHOXYCARBONYLPHENYL)MERCAPTO(I) TO ETHOXYCARBONYL-7-NITROBENZO[D]THIAZOLE-3-OXIDE(II), Chemicke listy, 91(9), 1997, pp. 672-674
The cyclization reaction kinetics has been studied in methanolic aceta
te, N-methylmorfoline and triethylamine buffers at a constans ionic st
renght I = 0.1 mol.1(-1). In the acetate buffers cyclization goes thro
ugh the dianionic intermediate In-1(2-) only and in the N-methylmorfol
ine and triethylamine buffers via the zwitterionic intermediate In-1(/-).