Výsledky vyhledávání - "B. A. Tertov"

Heterocyclic analogs of pleiadiene str]XXVI. Reaction of 1-methylperimidine and 1-methyl-2-chloroperimidine with alkali metals and their naphthalenides

Autor: Alexander F. Pozharskii, O. Yu. Okhlobystin, B. A. Tertov, L. P. Smirnova

Publikováno v: Chemistry of Heterocyclic Compounds. 13:673-678

1-Methylperimidine reacts with alkali metals or their naphthalenides to give, depending on the nature of the metal and the experimental conditions, an anion radical or a dianion. The latter are converted to a mixture of 1-methyl- and 1-methy1-2,3-dih

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6f8c5dfa0caa7970ed8180a175dd9b35
https://doi.org/10.1007/bf00480679

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Investigation of the reaction of 1,2,3-trimethyl-2-phenylbenzimidazoline with dehydrogenating reagents by EPR spectroscopy

Autor: A. N. Suslov, O. Yu. Okhlobystin, E. P. Ivakhnenko, Anatolii S. Morkovnik, E. S. Klimov, B. A. Tertov

Publikováno v: Chemistry of Heterocyclic Compounds. 23:525-529

The reaction of 1,2,3-trimethyl-2-phenylbenzimidazoline with a number of reagents that manifest dehydrogenating properties with respect to benziraidazolines was studied by EPR spectroscopy. These reagents convert 1,2,3-trimethyl-2-phenylbenzimidazoli

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3990bc3e0c108d768f8854c8cb25ab52
https://doi.org/10.1007/bf00476380

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Evolution of hydrogen in the reaction of hydroheteroaromatic compounds with dehydrogenating agents

Autor: N. T. Berberova, Yu. G. Bogachev, O. Yu. Okhlobystin, E. P. Ivakhnenko, B. A. Tertov, Anatolii S. Morkovnik

Publikováno v: Chemistry of Heterocyclic Compounds. 24:168-173

The yields of molecular hydrogen in the reactions of benzimidazolines 1,2-dihydropyrimidines with a number of dehydrogenating agents have been determined. The formation of hydrogen is due to breakdown of the cation-radicals of the hydrohetarenes form

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::412fab83e9c80ee713c13dd6c652d206
https://doi.org/10.1007/bf00473326

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Behavior of N-alkoxybenzimidzoles with respect to nucleophilic reagents. Attempts to synthesize N-hydroxy-2-aminobenzimidazoles

Autor: M. M. Medvedeva, V. V. Bessonov, V. V. Kuz'menko, Alexander F. Pozharskii, B. A. Tertov

Publikováno v: Chemistry of Heterocyclic Compounds. 15:166-172

Various possibilities for the synthesis of N-hydroxy- and N-alkoxy derivatives of 2-aminobenzimidazoles — reductive cyclization of o-nitrophenylureas, the action of sodium amide on 1-alkoxybenzimidazoles, the ammonolysis of 1-alkoxy-2-iodobenzimida

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::73d24da1980f1d718ea63929e7c138f0
https://doi.org/10.1007/bf00480362

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Synthesis and transformations of 2,3-dioxo-2,3-dihydroimidazo [1,2-a]-benzimidazole derivatives

Autor: A. M. Simonov, G. M. Suvorova, B. A. Tertov, Yu. V. Koshchienko, E. N. Malysheva

Publikováno v: Chemistry of Heterocyclic Compounds. 12:1151-1154

9-(H)Alkyl-2,3-dioxo-2,3-dihydroimidazo[1,2-a]benzimidazoles were synthesized by the action of oxalyl chloride on 2-amino-1(H)alkylbenzimidazoles and subsequent cyclization of the resulting 2-amino-1-(H)alkyl-3-chlorooxalylbenzimidazolium chlorides i

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::dc078bba9b750001f5d3770f47e273a3
https://doi.org/10.1007/bf00945604

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