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N. N. Kostikova

Researcher at Russian Academy of Sciences

Publications -  8
Citations -  31

N. N. Kostikova is an academic researcher from Russian Academy of Sciences. The author has contributed to research in topics: Alkylation & Chemistry. The author has an hindex of 3, co-authored 6 publications receiving 22 citations.

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Synthesis, S-alkylation, and fungicidal activity of 4-(benzylideneamino)thioglycolurils

TL;DR: In this article, a series of 1,3-disubstituted 4-benzylideneamino-5thioxohexahydroimidazo[4,5-d]imidazol-2(1H)-ones (thioglycolurils) was synthesized via the reaction of 5,7-disubsubstitized 3-thioxoperhydroIMidazo [4, 5-e]-1,2,4-triazin-6-ones with hydroxy-, alkoxy-, and
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Synthesis of New Imidazo[4,5-e][1,3]thiazolo-[3,2-b][1,2,4]triazine Derivatives

TL;DR: In this paper, (Z)-6-aryl(hetaryl)methylidene derivatives of imidazo[4,5-e][1,3]thiazolo[3,2-b]-[1,2,4]triazine-2,7-diones were synthesized by aldol-crotonic condensation.
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Functionally substituted aromatic aldehydes as reagents in the synthesis of new substituted thioglycolurils

TL;DR: In this paper, a simple approach to the synthesis of 2-(4(2)-(((4,6-dialkyl-5-oxo-2-thioxohexahydroimidazo[4,5-d]imidazol1(2H)-yl)imino)methyl)phenoxy)acetates or acetamides (new substituted thioglycolurils) was developed.
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Synthesis and Antimicrobial Activity of Phenylthioand Benzylsulfonylacetic Acids Based on 2-amino-5-alkyl(arylalkyl)-1,3,4-thiadiazoles

TL;DR: A series of N-(5-alkyl-1,3,4-thiadiazol-2-yl)-2-(phenylthio)acetamides and 2-(benzylsulfonyl)-N-(5 -alkyl]-1, 3, 4thiadiadiazool 2-yl) were synthesized and tested for biological activity as discussed by the authors.
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Synthesis of 1,3-dialkyl-4-[(arylmethylidene)amino]glycolurils

TL;DR: In this paper, a method for the synthesis of 1,3-dialkyl-4-[(arylmethylidene)amino]glycolurils was developed based on nucleophilic substitution of the sulfur atom with the oxygen atom in the corresponding thioglycoluril via alkylation of the latter followed by acid hydrolysis of alkylsulfanyl derivatives of thioglobalurils, both with the isolation of alknsulfanyl intermediates and by the one-pot method.