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177 results on '"Beletskaya, I.P."'

2. Contributors

Author

Bao, Ming, primary, Beletskaya, I.P., additional, Brown, Ainka T., additional, Chupakhin, Oleg N., additional, Downer-Riley, Nadale K., additional, Echeverry-Gonzalez, Carlos A., additional, Fatykhov, Ramil F., additional, Gandeepan, Parthasarathy, additional, Ghosh, Pranab, additional, Gonçalves, Raoni Schroeder B., additional, Karuppasamy, Muthu, additional, Khalymbadzha, Igor A., additional, Kouznetsov, Vladimir V., additional, de los Santos, Jesús M., additional, de Mariz e Miranda, Leandro Soter, additional, Menges, Nurettin, additional, Mitra, Bijeta, additional, Mitrofanov, A.Yu., additional, Ochoa de Retana, Ana M., additional, Palacios, Francisco, additional, Pariyar, Gyan Chandra, additional, Rusinov, Vladimir L., additional, Sridharan, Vellaisamy, additional, Vachan, B.S., additional, Xie, Zhilong, additional, Yamamoto, Yoshihiko, additional, and Zhang, Sheng, additional

Published
2021
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10. Synthesis of mono-, di-, and trisilyl-substituted alkenes via the hydrosilylation of nethylenecyclopropanes catalyzed by Rh(I) complexes

Author

Bessmertnykh, A.G., Blinov, K.A., Grishin, Yu. K., Donskaya, N.A., Tveritinova, E.V., Yur'eva, N.M., and Beletskaya, I.P.

Subjects
Olefins -- Analysis, Cyclic compounds -- Analysis, Hexane -- Analysis, Biological sciences, Chemistry
Abstract

A novel method of synthesizing organosilanes were designed featuring the use of H2PtCl6 and Rh complexes, including tris(triphenylphosphine)carbonylrhodium chloride as catalysts and methylenecyclopropanes as starting material. Hydrosilylation of the starting material resulted in the bond lysis of the cyclopropane ring, leading to monosilylated olefins. Methylenecyclopropanes with silanes containing vinylcyclopropane and methylenecyclopropane moieties resulted in di- and trisilylated olefins.

Published
1997

13. α,α-Difluoro-β-ketophosphonates on a tetraazamacrocyclic platform: Synthesis and inhibitory activity against protein tyrosine phosphatases

Author

Khavrienko, D.I., Kobzar, O.L., Shevchuk, M.V., Romanenko, V.D., Kobelev, S.M., Averin, A.D., Beletskaya, I.P., Vovk, A.I., and Kukhar, V.P.

Subjects
Хімія
Abstract

The present study offers a new approach for designing inhibitors of protein tyrosine phosphatases. We have synthesized the cyclam derivatives with α,α-difluoro-β-ketophosphonate fragments covalently attached to tetraazamacrocyclic scaffold, which is known to be of medical interest. The obtained functionalized macrocycles were evaluated as inhibitors of PTP1B, TC-PTP, CD45, and other protein tyrosine phosphatases. Запроновано новий пiдхiд до розробки iнгiбiторiв протеїнтирозинфосфатаз. Синтезовано похiднi цикламу з α,α-дифторо-β-кетофосфонатними фрагментами, ковалентно зв’язаними з тетраазамакроциклiчною платформою. Отриманi функцiоналiзованi макроцикли було дослiджено як iнгiбiтори PTP1B, TC-PTP, CD45 та iнших протеїнтирозинфосфатаз. Предложен новый поход к разработке ингибиторов протеинтирозинфосфатаз. Синтезированы производные циклама с α,α-дифтор-β-кетофосфонатными фрагментами, ковалентно связанными с тетраазамакроциклической платформой. Полученные функционализированные макроциклы были изучены в качестве ингибиторов PTP1B, TC-PTP, CD45 и других протеинтирозинфосфатаз.

Published
2014

22. Conjugated G0 Metallo-Dendrimers, Functionalized with Tridentate 'Pincer' -type Ligands

Author

Koten, G. van, Beletskaya, I.P., Chuchuryukin, A.V., Dijkstra, H.P., and Klink, G.P.M. van

Subjects
Scheikunde
Abstract

1, 3,5-Tris{3,5-bis[(diphenylphosphino)methyl]phenylethynyl}benzene (1) and hexakis{3,5-bis[(diphenylphosphino)methyl]phenylethynyl}benzene (2) have been synthesized and characterized. Furthermore, 1 was successfully cyclopalladated.

Published
2000

23. Acetylene-bridged P,C,P'-Ligands and Corresponding Cyclopalladated Compounds

Author

Koten, G. van, Beletskaya, I.P., Chuchuryukin, A.V., Dijkstra, H.P., and Klink, G.P.M. van

Subjects
Scheikunde
Abstract

Bis-'pincer'-cyclopalladates 1 and 2 containing an ethynediyl- or a butadiynediyl-bridge have been synthesized, characterized and used as precatalysts in the Heck reaction.

Published
2000

28. Synthesis and Catalytic Properties of Di- and Trinuclear Palladium Complexes with PCP-Pincer Ligand

Author

Homogene katalyse en materialen, Universiteit Utrecht, Dep Scheikunde, Beletskaya, I.P., Chuchuryukin, A.V., van Koten, G., Dijkstra, H.P., van Klink, G.P.M., Kashin, A.N., Nefedov, S.E., Eremenko, I.L., Homogene katalyse en materialen, Universiteit Utrecht, Dep Scheikunde, Beletskaya, I.P., Chuchuryukin, A.V., van Koten, G., Dijkstra, H.P., van Klink, G.P.M., Kashin, A.N., Nefedov, S.E., and Eremenko, I.L.

Published
2003

42. Exchange of organometallic compounds with mercury metal

Author

Butin, K.P., Gunkin, I.F., Petri, R., Beletskaya, I.P., and Reutov, O.A.

Abstract

Kinetic study of the interaction of di-p-anisylthallium chloride with mercury metal, in pyridine, ethylenediamine, or dimethyl sulfoxide solutions, show that in the former two solvents with the following experimental conditions: solution volume 10 ml, mercury surface area 10 cm2, 60°C, and without stirring of mercury, the Hg/Tl exchange occurs via the homogeneous reaction (80–90 percent) with dissolved mercury. In DMSO, under the same experimental conditions, the contribution of the homogeneous reaction is nearly the same as that of the heterogeneous one. This was determined by the study of the experimental exchange rate dependence on organic phase volume, and mercury or di-p-anisylthallium chloride solubilities in the solvents, as well as from analysis of kinetic curves for the exchange in saturated and unsaturated solutions of mercury metal in the solvents studied.

Published
1976
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43. Synthesis of substituted cinnamic acids and cinnamonitriles via palladium catalyzed coupling reactions of aryl halides with acrylic acid and acrylonitrile in aqueous media

Author

Bumagin, N.A., More, P.G., and Beletskaya, I.P.

Abstract

The palladium-catalysed coupling reactions of aryl halides with acrylic acid and acrylonitrile in the presence of a base (NaHCO3or K2CO3) in water provide a novel and efficient and very small method for the synthesis of substituted cinnamic acids and cinnamonitriles in high yields. NaHCO3or K2CO3effectively acts as a base in the reaction at elevated temperature 80–100°C). The reaction can be carried out with higher velocity and at low temperature (50–60°C), using CH3COOK as a base.

Published
1989
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44. Modern Trends of Organic Chemistry in Russian Universities

Author

Konovalov A.I., Antipin I.S., Burilov V.A., Madzhidov T.I., Kurbangalieva A.R., Nemtarev A.V., Solovieva S.E., Stoikov I.I., Mamedov V.A., Zakharova L.Y., Gavrilova E.L., Sinyashin O.G., Balova I.A., Vasilyev A.V., Zenkevich I.G., Krasavin M.Y., Kuznetsov M.A., Molchanov A.P., Novikov M.S., Nikolaev V.A., Rodina L.L., Khlebnikov A.F., Beletskaya I.P., Vatsadze S.Z., Gromov S.P., Zyk N.V., Lebedev A.T., Lemenovskii D.A., Petrosyan V.S., Nenaidenko V.G., Negrebetskii V.V., Baukov Y.I., Shmigol’ T.A., Korlyukov A.A., Tikhomirov A.S., Shchekotikhin A.E., Traven’ V.F., Voskresenskii L.G., Zubkov F.I., Golubchikov O.A., Semeikin A.S., Berezin D.B., Stuzhin P.A., Filimonov V.D., Krasnokutskaya E.A., Fedorov A.Y., Nyuchev A.V., Orlov V.Y., Begunov R.S., Rusakov A.I., Kolobov A.V., Kofanov E.R., Fedotova O.V., Egorova A.Y., Charushin V.N., Chupakhin O.N., Klimochkin Y.N., Osyanin V.A., Reznikov A.N., Fisyuk A.S., Sagitullina G.P., Aksenov A.V., Aksenov N.A., Grachev M.K., Maslennikova V.I., Koroteev M.P., Brel’ A.K., Lisina S.V., Medvedeva S.M., Shikhaliev K.S., Suboch G.A., Tovbis M.S., Mironovich L.M., Ivanov S.M., Kurbatov S.V., Kletskii M.E., Burov O.N., Kobrakov K.I., Kuznetsov D.N., Konovalov A.I., Antipin I.S., Burilov V.A., Madzhidov T.I., Kurbangalieva A.R., Nemtarev A.V., Solovieva S.E., Stoikov I.I., Mamedov V.A., Zakharova L.Y., Gavrilova E.L., Sinyashin O.G., Balova I.A., Vasilyev A.V., Zenkevich I.G., Krasavin M.Y., Kuznetsov M.A., Molchanov A.P., Novikov M.S., Nikolaev V.A., Rodina L.L., Khlebnikov A.F., Beletskaya I.P., Vatsadze S.Z., Gromov S.P., Zyk N.V., Lebedev A.T., Lemenovskii D.A., Petrosyan V.S., Nenaidenko V.G., Negrebetskii V.V., Baukov Y.I., Shmigol’ T.A., Korlyukov A.A., Tikhomirov A.S., Shchekotikhin A.E., Traven’ V.F., Voskresenskii L.G., Zubkov F.I., Golubchikov O.A., Semeikin A.S., Berezin D.B., Stuzhin P.A., Filimonov V.D., Krasnokutskaya E.A., Fedorov A.Y., Nyuchev A.V., Orlov V.Y., Begunov R.S., Rusakov A.I., Kolobov A.V., Kofanov E.R., Fedotova O.V., Egorova A.Y., Charushin V.N., Chupakhin O.N., Klimochkin Y.N., Osyanin V.A., Reznikov A.N., Fisyuk A.S., Sagitullina G.P., Aksenov A.V., Aksenov N.A., Grachev M.K., Maslennikova V.I., Koroteev M.P., Brel’ A.K., Lisina S.V., Medvedeva S.M., Shikhaliev K.S., Suboch G.A., Tovbis M.S., Mironovich L.M., Ivanov S.M., Kurbatov S.V., Kletskii M.E., Burov O.N., Kobrakov K.I., and Kuznetsov D.N.

Abstract

This review is devoted to the scientific achievements of the departments of organic chemistry in higher schools of Russia within the past decade. © 2018, Pleiades Publishing, Ltd.

45. Some problems of the teaching of organic chemistry in universities of Russia

Author

Beletskaya I.P., Lukashev N.V., Vatsadze S.Z., Nenajdenko V.G., Negrebetskii V.V., Baukov Y.I., Belavin I.Y., Butseeva A.A., Beloborodov V.L., Selivanova I.A., Il’yasov I.R., Nevskaya E.Y., Sorokina E.A., Syrbu S.A., Usol’tseva N.V., Danilin A.A., Nechaeva O.N., Purygin P.P., Deryabina G.I., Aksenov A.V., Aksenova I.V., Ovcharov S.N., Gavrilova E.L., Uryadov V.G., Zakharov V.M., Sinyashin O.G., Klochkova I.N., Krylatova Y.G., Skornyakov Y.V., Ovchinnikov K.L., Kolobov A.V., Kustova T.P., Beletskaya I.P., Lukashev N.V., Vatsadze S.Z., Nenajdenko V.G., Negrebetskii V.V., Baukov Y.I., Belavin I.Y., Butseeva A.A., Beloborodov V.L., Selivanova I.A., Il’yasov I.R., Nevskaya E.Y., Sorokina E.A., Syrbu S.A., Usol’tseva N.V., Danilin A.A., Nechaeva O.N., Purygin P.P., Deryabina G.I., Aksenov A.V., Aksenova I.V., Ovcharov S.N., Gavrilova E.L., Uryadov V.G., Zakharov V.M., Sinyashin O.G., Klochkova I.N., Krylatova Y.G., Skornyakov Y.V., Ovchinnikov K.L., Kolobov A.V., and Kustova T.P.

Abstract

[No abstract available]

46. Organic chemistry. History and mutual relations of universities of Russia

Author

Antipin I.S., Kazymova M.A., Kuznetsov M.A., Vasilyev A.V., Ishchenko M.A., Kiryushkin A.A., Kuznetsova L.M., Makarenko S.V., Ostrovskii V.A., Petrov M.L., Solod O.V., Trishin Y.G., Yakovlev I.P., Nenaidenko V.G., Beloglazkina E.K., Beletskaya I.P., Ustynyuk Y.A., Solov’ev P.A., Ivanov I.V., Malina E.V., Sivova N.V., Negrebetskii V.V., Baukov Y.I., Pozharskaya N.A., Traven’ V.F., Shchekotikhin A.E., Varlamov A.V., Borisova T.N., Lesina Y.A., Krasnokutskaya E.A., Rogozhnikov S.I., Shurov S.N., Kustova T.P., Klyuev M.V., Khelevina O.G., Stuzhin P.A., Fedorov A.Y., Gushchin A.V., Dodonov V.A., Kolobov A.V., Plakhtinskii V.V., Orlov V.Y., Kriven’ko A.P., Fedotova O.V., Pchelintseva N.V., Charushin V.N., Chupakhin O.N., Klimochkin Y.N., Klimochkina A.Y., Kuryatnikov V.N., Malinovskaya Y.A., Levina A.S., Zhuravlev O.E., Voronchikhina L.I., Fisyuk A.S., Aksenov A.V., Aksenov N.A., Aksenova I.V., Antipin I.S., Kazymova M.A., Kuznetsov M.A., Vasilyev A.V., Ishchenko M.A., Kiryushkin A.A., Kuznetsova L.M., Makarenko S.V., Ostrovskii V.A., Petrov M.L., Solod O.V., Trishin Y.G., Yakovlev I.P., Nenaidenko V.G., Beloglazkina E.K., Beletskaya I.P., Ustynyuk Y.A., Solov’ev P.A., Ivanov I.V., Malina E.V., Sivova N.V., Negrebetskii V.V., Baukov Y.I., Pozharskaya N.A., Traven’ V.F., Shchekotikhin A.E., Varlamov A.V., Borisova T.N., Lesina Y.A., Krasnokutskaya E.A., Rogozhnikov S.I., Shurov S.N., Kustova T.P., Klyuev M.V., Khelevina O.G., Stuzhin P.A., Fedorov A.Y., Gushchin A.V., Dodonov V.A., Kolobov A.V., Plakhtinskii V.V., Orlov V.Y., Kriven’ko A.P., Fedotova O.V., Pchelintseva N.V., Charushin V.N., Chupakhin O.N., Klimochkin Y.N., Klimochkina A.Y., Kuryatnikov V.N., Malinovskaya Y.A., Levina A.S., Zhuravlev O.E., Voronchikhina L.I., Fisyuk A.S., Aksenov A.V., Aksenov N.A., and Aksenova I.V.

Abstract

The review describes the history of development of organic chemistry in higher schools of Russia over a period of 170 years, since the emergence of organic chemistry in our country till now. © 2017, Pleiades Publishing, Ltd.

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