Works matching IS 00093122 AND DT 2017 AND VI 53 AND IP 10
Results: 18
Synthesis of 2-halo-2 Н-azirine-2-carboxylic acid amides and esters by isomerization of 5-(dialkylamino/alkoxy)-substituted isoxazoles, catalyzed by iron(II) sulfate.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 10, p. 1068, doi. 10.1007/s10593-017-2172-z
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Heterocyclic Analogs of 5,12-Naphthacenequinone 14. Synthesis of naphtho[2,3- f]indole-3-carboxylic Acid Derivatives.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 10, p. 1072, doi. 10.1007/s10593-017-2173-y
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Synthesis and inhibitory activity of 1,3-(adamantan-1(2)-yl)- imidazolidine-2,4,5-triones and 3,3'-(adamantan-1-yl)- bis(1-alkylimidazolidine-2,4,5-triones).
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 10, p. 1080, doi. 10.1007/s10593-017-2174-x
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Purity analysis method of 1-methyl-3,5-dinitro-1 H-1,2,4-triazole.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 10, p. 1084, doi. 10.1007/s10593-017-2175-9
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Synthesis of polyfunctionalized 1,1'-(α,ω-alkanediyl)bis(1,2,3,4-tetrahydropyridines).
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 10, p. 1098, doi. 10.1007/s10593-017-2176-8
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Microwave-mediated synthesis of poly{[ p-(azidomethyl)styrene]- co-(5-vinyltetrazole)} as an energetic polymer.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 10, p. 1090, doi. 10.1007/s10593-017-2177-7
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Synthesis and Analgesic Activity of bis(3,4-dihydroquinoxalin-2(1 H)-one) and bis(3,4-dihydro-2 H-1,4-benzoxazin-2-one) Derivatives.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 10, p. 1094, doi. 10.1007/s10593-017-2178-6
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Cycloisomerization - a straightforward way to benzo[ h]quinolines and benzo[ c]acridines.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 10, p. 1103, doi. 10.1007/s10593-017-2179-5
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An efficient and green synthesis of polyfunctionalized spirothiazolidin-4-ones using sulfonated mesoporous silica as a reusable catalyst.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 10, p. 1148, doi. 10.1007/s10593-017-2185-7
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- Article
N-Substituted cyanacetohydrazides in the synthesis of 3,3-dialkyl-1,2,3,4-tetrahydroisoquinolines by Ritter reaction.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 10, p. 1114, doi. 10.1007/s10593-017-2180-z
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- Article
The addition of β-ketoacids to 4-(trifluoromethyl)pyrimidin- 2(1 Н)-ones with decarboxylation: an effective method for the synthesis of 4-(2-oxoalkyl)-6-(trifluoromethyl)-3,4-dihydropyrimidin-2-ones.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 10, p. 1124, doi. 10.1007/s10593-017-2182-x
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- Article
Chemospecific reactions of as-triazine ring reduction in sulfonyl derivatives of pyrazolo[5,1- c][1,2,4]triazines.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 10, p. 1128, doi. 10.1007/s10593-017-2183-9
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[1,2,4]Triazino[2,3- с]quinazolines 2*. Synthesis, structure, and anticonvulsant activity of new 3′-R-spiro[(aza/oxa/thia)cycloalkyl-1(3, 4),6′-[1,2,4]triazino[2,3- c]quinazolin]-2′(7′ H)-ones.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 10, p. 1134, doi. 10.1007/s10593-017-2184-8
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- Article
Synthesis of diheteroaryl sulfides via chemoselective reaction of 4,6-diaminopyrimidine-2(1 H)-thione with haloheteroaryl compounds.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 10, p. 1120, doi. 10.1007/s10593-017-2181-y
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A unique example of noncatalyzed [3+2] cycloaddition involving (2 E)-3-aryl-2-nitroprop-2-enenitriles.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 10, p. 1161, doi. 10.1007/s10593-017-2186-6
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Synthesis of dithienoquinazolines from pyrimidines via intramolecular nucleophilic aromatic substitution of hydrogen.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 10, p. 1156, doi. 10.1007/s10593-017-2188-4
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Synthesis of Se-N and Te-N bond-containing heterocycles.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 10, p. 1061, doi. 10.1007/s10593-017-2171-0
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Unexpected transformations of 11-acetyl-8-bromo-2-methyl-5,6-dihydro-2 H-2,6-methano-1,3,5-benzoxadiazocin-4(3 H)-one(thione).
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 10, p. 1163, doi. 10.1007/s10593-017-2187-5
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