Acyclic analogs of nucleosides. Synthesis of hydroxyalkyl derivatives of 2-trifluoromethyl- and 2-trifluoromethylthiobenzimidazole
Identifieur interne : 001544 ( Main/Exploration ); précédent : 001543; suivant : 001545Acyclic analogs of nucleosides. Synthesis of hydroxyalkyl derivatives of 2-trifluoromethyl- and 2-trifluoromethylthiobenzimidazole
Auteurs : A. É. Yavorskii [Russie] ; A. V. Stetsenko [Russie] ; I. V. Gogoman [Russie] ; V. N. Boiko [Russie] ; S. G. Zavgorodnii [Russie] ; A. I. Sobko [Russie] ; V. N. Tatskaya [Russie] ; V. G. Kvachev [Russie] ; V. L. Florent'Ev [Russie]Source :
- Chemistry of Heterocyclic Compounds [ 0009-3122 ] ; 1988-05-01.
English descriptors
- Teeft :
- Absolute acetonitrile, Acyclic, Acyclic analogs, Analog, Antivirus activity, Biological activity, Characteristic fragment ions, Cytopathogenic activity, Ester, Heterocyclic base, Khimiya geterotsiklicheskikh soedinenii, Mass spectra, Methanol solution, Mmole, Nucleoside, Nucleoside analogs, Original article, Potassium carbonate, Primary hydroxy groups, Relative intensity, Swine enterovirus, Trimethylsilyl derivatives, Triplet signals, Viia, Viib, Weak field.
Abstract
Abstract: 1-(2,3-Dihydroxypropyl)-, 1-(4-hydroxy-2-oxabutyl)-, 1-(3-hydroxymethyl-4-hydroxy-2-oxabutyl)-, 1-(1,5-dihydroxy-3-oxa-2-pentyl)-, 1-(5-hydroxy-3-oxa-2-pentyl)-, and 1-(4,5-dihydroxy-2-oxapentyl)-2-trifluoromethyl- and -2-trifluoromethylthiobenzimidazoles were obtained by condensation of trimethylsilyl derivatives of 2-substituted benzimidazoles with alkylating agents in the presence of SnCl4, or by direct alkylation of the sodium salts of the heterocycles.
Url:
DOI: 10.1007/BF00755691
Affiliations:
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Le document en format XML
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<series><title level="j">Chemistry of Heterocyclic Compounds</title>
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<profileDesc><textClass><keywords scheme="Teeft" xml:lang="en"><term>Absolute acetonitrile</term>
<term>Acyclic</term>
<term>Acyclic analogs</term>
<term>Analog</term>
<term>Antivirus activity</term>
<term>Biological activity</term>
<term>Characteristic fragment ions</term>
<term>Cytopathogenic activity</term>
<term>Ester</term>
<term>Heterocyclic base</term>
<term>Khimiya geterotsiklicheskikh soedinenii</term>
<term>Mass spectra</term>
<term>Methanol solution</term>
<term>Mmole</term>
<term>Nucleoside</term>
<term>Nucleoside analogs</term>
<term>Original article</term>
<term>Potassium carbonate</term>
<term>Primary hydroxy groups</term>
<term>Relative intensity</term>
<term>Swine enterovirus</term>
<term>Trimethylsilyl derivatives</term>
<term>Triplet signals</term>
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<front><div type="abstract" xml:lang="en">Abstract: 1-(2,3-Dihydroxypropyl)-, 1-(4-hydroxy-2-oxabutyl)-, 1-(3-hydroxymethyl-4-hydroxy-2-oxabutyl)-, 1-(1,5-dihydroxy-3-oxa-2-pentyl)-, 1-(5-hydroxy-3-oxa-2-pentyl)-, and 1-(4,5-dihydroxy-2-oxapentyl)-2-trifluoromethyl- and -2-trifluoromethylthiobenzimidazoles were obtained by condensation of trimethylsilyl derivatives of 2-substituted benzimidazoles with alkylating agents in the presence of SnCl4, or by direct alkylation of the sodium salts of the heterocycles.</div>
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