Synthesis, Structure, and Analgesic Properties of Phosphorylated Dihydro-1,4-Benzodiazepin-2-Ones von Pavlovskii, V. I., Gololobov, Yu. G., Andronati, S. A., Voronenko, E. V., Kabanova, T. A., Khalimova, E. I., Krasnova, I. Yu, Khrustalev, V. N.

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1,5-Thione-thiol isomerization of 3-O-phosphorylated 1,4-benzodiazepine von Gololobov, Yu. G., Krasnova, I. Yu, Barabanov, S. V., Makarov, M. V., Khrustalev, V. N., Andronati, S. A., Pavlovskii, V. I.

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Transformations of trisubstituted CH-acids von Gololobov, Yu. G., Krasnova, I. Yu

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Technique of the laparoscopic pelvic exenteration von Galliamov, E. A., Biktimirov, R. G., Sergeev, V. P., Aminova, L. N., Sanzharov, A. E., Agapov, M. A., Volodin, D. I., Gallyamov, Е. E., Gololobov, G. Yu

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Coupling of methylene-active compounds through a methylene bridge by the action of bis(dimethylamino)methane 1. Synthesis of 2,4-bis(diphenylphosphoryl)glutaronitrile von Gololobov, Yu. G., Barabanov, S. V., Peregudov, A. S., Petrovskii, P. V., Khrustalev, V. N.

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Cleavage of the P-C bond in the reactions of phosphoryl-substituted CH acids with 1-fluoro-2,4,6-trinitrobenzene in the presence of bases von Gololobov, Yu. G., Krasnova, I. Yu, Matveeva, E. V., Petrovskii, P. V.

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Synthesis, structural and spectral features of CH-Acids: Amides of 2,4-dinitrophenylcyanoacetic acid and their ammonium salts von Gololobov, Yu. G., Golding, I. R., Barabanov, S. V., Khrustalev, V. N., Garbuzova, I. A., Peregudov, A. S.

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Properties and application of 2-Cyanoacrylates von Gololobov, Yu. G.

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Triethylamine-assisted reaction between 2,4-dinitrofluorobenzene and malononitrile von Golding, I. R., Starikova, Z. A., Senchenya, N. G., Petrovskii, P. V., Garbuzova, I. A., Gololobov, Yu. G.

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Synthesis and structures of the CH acid salts obtained in the reactions of malonic acid esters and malononitriles with 2,4,6-trinitrohalobenzenes in the presence of triethylamine von Gololobov, Yu. G., Barabanov, S. V., Peregudov, A. S., Petrovskii, P. V., Starikova, Z. A., Khrustalev, V. N., Garbuzova, I. A.

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On the nature of intermediates in the reactions of carbanions of diethyl arylmalonates with isocyanates von Gololobov, Yu. G., Slepchenkov, N. V., Petrovskii, P. V., Nelyubina, Yu. V.

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Cyanoacrylate-based adhesives von Senchenya, N. G., Guseva, T. I., Gololobov, Yu. G.

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Phosphorus-containing 1, 3-zwitterions formed in the reaction of tributylphosphine with 3-aryl-2-cyanoacrylates von Slepchenkov, N. V., Peregudov, A. S., Senchenya, N. G., Petrovskii, P. V., Khrustalev, V. N., Garbuzova, I. A., Gololobov, Yu. G.

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Synthesis and structure of 2,4-dinitrophenylcyanoacetamide derivatives as CH acids and their organic salts von Gololobov, Yu. G., Gol’ding, I. R., Terrie, F., Petrovskii, P. V., Lyssenko, K. A., Garbuzova, I. A.

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Intramolecular 1,3-C-C migration of fluorine in a σ complex formed by 2,4,6-trinitrofluorobenzene and the P-zwitterion von Gololobov, Yu. G., Linchenko, O. A., Petrovskii, P. V., Garbuzova, I. A., Khrustalev, V. N.

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Reactions of distabilized β-dicarbonyl sulfonium and iodonium ylides with isocyanates von Gololobov, Yu. G., Golding, I. R., Galkina, M. A., Lokshin, B. V., Garbuzova, I. A., Petrovskii, P. V., Starikova, Z. A., Averkiev, B. B.

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Novel reactions of arylmalonate carbanions. The reaction with phenyl isocyanate resulting in carbamates by 1,3-C→N migration of the ethoxycarbonyl group von Linchenko, O. A., Krasnova, I. Yu, Petrovskii, P. V., Garbuzova, I. A., Khrustalev, V. N., Gololobov, Yu. G.

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Novel nucleophilic aromatic substitution of the fluorine atom yielding a stable heptatrienide structure von Gololobov, Yu. G., Linchenko, O. A., Starikova, Z. A., Garbuzova, I. A., Petrovskii, P. V.

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C-N migration of allyl-and propargyloxycarbonyl groups von Gololobov, Yu. G., Senchenya, N. G., Linchenko, O. A., Petrovskii, P. V., Garbuzova, I. A.

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C→N migration of methoxycarbonyl and acetyl groups in reactions of functionally substituted carbanions with aryl isocyanates. Kinetics and mechanism of the reactions von Galkin, V. I., Bakhtiyarova, Yu. V., Mal’tsev, D. B., Galkina, I. V., Gololobov, Yu. G., Linchenko, O. A.

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