63500-83-4Relevant articles and documents
REACTIVITY AND TAUTOMERISM OF AZOLIDINES. XXXV. DUAL REACTIVITY OF AMBIDENT ANIONS OF 2-ARYLIMINOTHIAZOLIDIN-4-ONES
Ramsh, S. M.,Ginak, A. I.,Basova, Yu. G.,Shamina, L. P.
, p. 742 - 747 (2007/10/02)
The kinetics of the dual reaction of sodium salts of 2-aryliminothiazolidin-4-ones with dimethyl sulfate and methyl iodide in methanol at 25 deg C were studied.The overall methylation rate constant k1, the partial methylation constants at each reaction center k2 and k3 and their ratio k2/k3 obey the Hammet and Broensted equations.The contributions from the basicity and polarizability to the nucleophilicity of each reaction center were evaluated by means of the Edwards equation.
REACTIVITY AND TAUTOMERISM OF AZOLIDINES. XXXIX. ALKYLATION OF ALKALI-METAL SALTS OF 2-ARYLIMINOTHIAZOLIDIN-4-ONES IN THE SOLID PHASE
Basova, Yu. G.,Ramsh, S. M.,Ginak A. I.
, p. 867 - 870 (2007/10/02)
The effects of the counterion, the substituted group of the alkylating agent, and the substituent at the para position of the benzene ring on the direction of alkylation of the alkali-metal salts of 2-aryliminothiazolidin-4-ones in the solid phase were investigated.The ratio of the isomeric products from alkylation at the N2' and N3 nitrogen atoms with variations of the counterion and the substituted group varies in accordance with the principle of "hard" and "soft" acids and bases.The logarithms of the N2'/N3 ratios correlate with the Hammett ? constants.