S. Mammadov, S. Mammadova, N. Ladokhina
Nov 30, 2016
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Journal
Theoretical & Applied Science
Abstract
The alkoxylation and aminomethylation reactions of guanidine sulfamates were studied. It is found that ternary guanidine sulfamates reaction with alcohols and amines in the presence of formaldehyde is terminated with a high yield. Compounds obtained as dipolars are easily heterocyclisize with polarophiles forming functionally substituted pyrimidines. Synthesized compounds are studied as biocides by Hansch’s method. It was found that regardless of the heterocyclic fragment content have high bactericidal properties.