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ISPC Education and Innovation, Scranton, USA |
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* Scientific Article * Impact Factor 6.630 |
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Mammadov SA, Mammadova SI, Ladokhina NP, Kazimzade SK, Huseinov IS
PROPERTIES AND SYNTHESIS OF ALKOXY- AND AMINOMETHYLENE DERIVATIVE GUANIDINE SULFAMATES AND THEIR HETEROCYCLIZATION. |
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Full Article: PDF
Scientific Object Identifier: http://s-o-i.org/1.1/TAS-11-43-15
DOI: http://dx.doi.org/10.15863/TAS.2016.11.43.15
Language: English
Citation: Mammadov SA, Mammadova SI, Ladokhina NP, Kazimzade SK, Huseinov IS (2016) PROPERTIES AND SYNTHESIS OF ALKOXY- AND AMINOMETHYLENE DERIVATIVE GUANIDINE SULFAMATES AND THEIR HETEROCYCLIZATION. ISJ Theoretical & Applied Science, 11 (43): 77-84. Soi: http://s-o-i.org/1.1/TAS-11-43-15 Doi: http://dx.doi.org/10.15863/TAS.2016.11.43.15 |
Pages: 77-84
Published: 30.11.2016
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.
Key words: Alkoxymethyl, aminomethyl, guanidine sulfamate, polarophil, heterocyclization, bactericide
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