Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Alexander N. Shivanyuk"'
Autor:
Oleg Lukin, Sergey V. Ryabukhin, Andrey A. Tolmachev, Sergey E. Pipko, Alexander N. Shivanyuk, Andrey V. Bogolubsky, Dmytro Mykytenko
Publikováno v:
Tetrahedron. 67:3619-3623
A facile and versatile method for the synthesis of unsymmetrical ureas from readily available reagents is reported. In the first step trifluoroethylchloroformate is reacted with a stoichiometric amount of a primary amine to give an intermediate trifl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::acb6905866f742539d65aa260f60b6fb
https://doi.org/10.1016/j.tet.2011.03.101
https://doi.org/10.1016/j.tet.2011.03.101
Autor:
Andrey A. Tolmachev, Pavel V. Khodakovskiy, Sergey V. Ryabukhin, Alexander N. Shivanyuk, Dmitry S. Granat
Publikováno v:
Tetrahedron Letters. 49:3997-4002
New efficient one-pot methodology for the preparative synthesis of β-imidazolylpropionamides was elaborated. It is based on the addition of imidazole to the activated double bond of the intermediate acrylimidazolide in the reaction between diverse a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7165a0e2f4d84ac4c170e28462ea3ca3
https://doi.org/10.1016/j.tetlet.2008.04.096
https://doi.org/10.1016/j.tetlet.2008.04.096
Autor:
Andrey S. Plaskon, Dmitriy M. Volochnyuk, Sergey V. Ryabukhin, Alexander N. Shivanyuk, Oleg V. Shishkin, Eugeniy N. Ostapchuk, Andrey A. Tolmachev
Publikováno v:
Organic Letters. 9:4215-4218
The chlorotrimethylsilane-promoted Biginelli type reactions of aldehydes, thiourea, and cyanoketones led to a diverse set of tetrahydropyrimidine-2(1H)-thiones. Under similar conditions, thioureas, benzaldehyde, and cyanoacetamide reacted to give fir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf51e8b00c7fbac096bbc0019c37a287
https://doi.org/10.1021/ol701782v
https://doi.org/10.1021/ol701782v
Publikováno v:
Tetrahedron letters, 37(52), 9341-9344. Elsevier
An assembly of cation receptor 1 and anion receptor 2 via the hydrogen bonding melamine-barbiturate structural motif complexes sodium thiocyanate, sodium iodide, and sodium azide in apolar solvents.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b14ef28acf6981255eeddfb747b43754
https://doi.org/10.1016/s0040-4039(97)82959-0
https://doi.org/10.1016/s0040-4039(97)82959-0
Autor:
Andrey A. Tolmachev, Alexander N. Shivanyuk, Andrey V. Bogolubsky, Sergey E. Pipko, Dmytro Mykytenko, Sergey V. Ryabukhin, Oleg Lukin
Publikováno v:
ChemInform. 42
A facile and versatile method for the synthesis of unsymmetrical ureas from readily available reagents is reported. In the first step trifluoroethylchloroformate is reacted with a stoichiometric amount of a primary amine to give an intermediate trifl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2211a9cd9e619e61193ccf6a108489b
https://doi.org/10.1002/chin.201136086
https://doi.org/10.1002/chin.201136086
Autor:
Masakatsu Shibasaki, Miguel Yus, Stacy Bremner, Eamon Comer, Gjergji Shore, Sylvie Morin, Michael G. Organ, Erik Van der Eycken, Eugen Merkul, Dieter Dorsch, Thomas J. J. Müller, Sergey V. Ryabukhin, Eugeniy N. Ostapchuk, Andrey S. Plaskon, Dmitriy M. Volochnyuk, Alexander N. Shivanyuk, Andrey A. Tolmachev, Hassan Sheibani, Maryam Babaie, Soheila Behzadi, Minoo Dabiri, Mahboobeh Bahramnejad, Sahareh Bashiribod, Rahim Hekmatshoar, Sodeh Sadjadi, Mohammad Khorasani, Anatoliy I. Polyakov, Vera A. Eryomina, Lidiya A. Medvedeva, Nadezhda I. Tihonova, Anna V. Listratova, Leonid G. Voskressensky, Zeinab Esfandiarpoor, Julia A. Titova, Olga V. Fedorova, Irina G. Ovchinnikova, Marina S. Valova, Olga V. Koryakova, Gennady L. Rusinov, Valery N. Charushin
Publikováno v:
MCR 2009 ISBN: 9781441972699
We have been studying the development of new asymmetric two-center catalysis using rare earth alkoxides and bifunctional sugar and related ligands. In The Fourth International Conference on Multi-Component Reactions and Related Chemistry (MCR 2009),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2b12a71c335b464d40a751ded58b934
https://doi.org/10.1007/978-1-4419-7270-5_1
https://doi.org/10.1007/978-1-4419-7270-5_1
Autor:
Pavel V. Khodakovskiy, Alexander N. Shivanyuk, Oleg V. Shishkin, Dmitriy M. Volochnyuk, Andrey A. Tolmachev
Publikováno v:
ChemInform. 40
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26150c51282518672941f2bbd48899f2
https://doi.org/10.1002/chin.200908147
https://doi.org/10.1002/chin.200908147
Autor:
Dmitriy M. Volochnyuk, Alexander N. Shivanyuk, Sergey V. Ryabukhin, Andrey A. Tolmachev, Andrey S. Plaskon
Publikováno v:
ChemInform. 39
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::92d5be92707a757e33afd237cf4da1bd
https://doi.org/10.1002/chin.200849156
https://doi.org/10.1002/chin.200849156
Autor:
Sergey V. Ryabukhin, Andrey S. Plaskon, Alexander N. Shivanyuk, Andrey A. Tolmachev, Dmitriy M. Volochnyuk
Publikováno v:
ChemInform. 39
A facile and versatile procedure for the synthesis of 5-hetaryl-3-(2-hydroxybenzoyl)-1 H -pyrroles and 4-(2-hydroxybenzoyl)-1 H -pyrrole-2-carboxylic acid derivatives was established on the basis of TMSCl promoted recyclization of 3-formylchromone wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::635b47278c073a23eb9156a3e692eec2
https://doi.org/10.1002/chin.200843120
https://doi.org/10.1002/chin.200843120
Autor:
Andrey A. Tolmachev, Sergey V. Ryabukhin, Pavel V. Khodakovskiy, Dmitry S. Granat, Alexander N. Shivanyuk
Publikováno v:
ChemInform. 39
New efficient one-pot methodology for the preparative synthesis of β-imidazolylpropionamides was elaborated. It is based on the addition of imidazole to the activated double bond of the intermediate acrylimidazolide in the reaction between diverse a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd72516fb30e7b7002c5e80d3438696e
https://doi.org/10.1002/chin.200840118
https://doi.org/10.1002/chin.200840118