Zobrazeno 1 - 10
of 69
pro vyhledávání: '"E. O. Tsetlina"'
Autor:
N. A. Keiko, Tatyana A. Kuznetsova, M. G. Voronkov, V. A. Pestunovich, E. O. Tsetlina, V. V. Keiko
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 27:783-786
1. Cyanosilylated acrolein and 2-ethoxyacrolein isomerize in the presence of secondary amines and react with an excess of the latter to form derivatives of propionamide and N-substituted aminosilanes. 2. Unlike 1-cyano-1-trimethylsiloxy-2-ethoxy-2-pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::349e95e2bd7a3d1450ae72eaa6e4e19a
https://doi.org/10.1007/bf00925307
https://doi.org/10.1007/bf00925307
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 25:1765-1768
Eight new trans-1,2-disilylethylenes were synthesized by the hydrosilylation of (CH ≡ C)2Si(OCH3)CH3 with HSiCl3 and HSi(CH3)Cl2, and also of (CH3)3SiC ≡ CH, CH3O(CH3)2SiC ≡ CH, and CH3(CH3O)2SiC ≡ CH with HSi(CH3)(C6H5)Cl9 and of (CH3O)3SiC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b9906c530fdd9b0cdbfecbf5a9799c5
https://doi.org/10.1007/bf00921453
https://doi.org/10.1007/bf00921453
Publikováno v:
Chemistry of Heterocyclic Compounds. 15:269-273
Dispiro[bis(3-aminoindene)-1′,4;1′,5-(1,3-dithiolanes)] react readily with Cu+, Ag+, Hg+, and Hg2+ salts to give the corresponding bis(1-imino-3-indenyls) and methanedithiol derivatives. Bis(1-oxo-3-indenyls) are formed when the reaction is carri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7ac92e0be317a2f0ac7ebc4a08353c85
https://doi.org/10.1007/bf00474089
https://doi.org/10.1007/bf00474089
Autor:
E. O. Tsetlina, Tatyana A. Kuznetsova, M. G. Voronkov, N. A. Keiko, V. K. Roman, V. A. Pestunovich
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 26:363-366
1. The cyanosilylation of 2-ethoxyacrolein by trimethylcyanosilane occurs in the 1,2 position, under specific conditions there is a side reaction involving the dimerization of 2-ethoxyacrolein and the subsequent cyanosilylation of the dimer formed, v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::853cbd05ce42131412b8a883853441b4
https://doi.org/10.1007/bf00921852
https://doi.org/10.1007/bf00921852
Autor:
V. A. Pestunovich, Václav Chvalovský, Josef Pola, V. B. Pukhnarevich, Michail G. Voronkov, E. O. Tsetlina, B. A. Trofimov, L. I. Kopylova
Publikováno v:
Collection of Czechoslovak Chemical Communications. 41:391-394
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56bef9827d60dd537645ac5097d9d2ea
https://doi.org/10.1135/cccc19760391
https://doi.org/10.1135/cccc19760391
Autor:
S. A. Vol'shakova, Svetlana V. Kirpichenko, M. G. Voronkov, V. Khvalovskii, Boris A. Trofimov, Svetlana V. Amosova, N. N. Vlasova, E. O. Tsetlina, V. V. Keiko
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 28:389-393
The reaction of ethyl vinyl sulfide and divinyl sulfide with triethyl and triethoxysilane in the presence of H2PtCl6 and (Ph3P)3RhCl has been studied. The hydrosilylation of ethyl vinyl sulfide and divinyl sulfide proceeds nonselectively, giving a mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2dd84a4acf820cfbe0bb1a813367037
https://doi.org/10.1007/bf00925892
https://doi.org/10.1007/bf00925892
Autor:
E. O. Tsetlina, A. A. Bystritskii, V. A. Pestunovich, N. A. Keiko, M. G. Voronkov, Tatyana A. Kuznetsova
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 24:2645-2649
1. Depending on the nature of the catalyst and the temperature, the hydrosilylation of 2-ethoxyacrolein with diethylsilane in the presence of H2PtCl6 or colloidal nickel leads to the formation of the 1,2- and 1,4-addition products, and specifically 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d2cd90d20750a87162170d1fa74226e
https://doi.org/10.1007/bf01152865
https://doi.org/10.1007/bf01152865
Autor:
Svetlana V. Kirpichenko, M. G. Voronkov, E. O. Tsetlina, V. V. Keiko, V. A. Pestunovich, L. V. Sherstyannikova
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 24:319-322
1. The reaction of triethylsilane with 3-substituted 1-propyne derivatives (HC≡CCH2X) leads to the formation of the addition products both by the Farmer rule (trans-isomer) and contrary to it (gem-isomer). Electronegative substituents cause the pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::346e6282eb20a341f542e35f99ee67a0
https://doi.org/10.1007/bf00925777
https://doi.org/10.1007/bf00925777
Publikováno v:
Chemistry of Heterocyclic Compounds. 14:27-32
3-Aminoindene-1-thiones react readily with diazomethane to give the corresponding 4,4;5,5-dispiro-substituted 1,3-dithiolanes. The production of both 2,2-spiro-substituted thiiranes and products of desulfuration of the latter is possible in the react
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b74d3f08e04e6984bc9c62a0dad5986
https://doi.org/10.1007/bf00635937
https://doi.org/10.1007/bf00635937
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 22:1764-1767
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1531d649fb5767daf518c347a1cc026
https://doi.org/10.1007/bf00932110
https://doi.org/10.1007/bf00932110