Zobrazeno 1 - 10
of 250
pro vyhledávání: '"E F Litvin"'
Publikováno v:
Journal of Chromatography A. 1084:13-17
A variant of electroosmotic thin-layer chromatography is suggested with the use of low volatility compounds as mobile phases aimed at drastically decreasing the evaporation of the mobile phase and improving the reproducibility of the method. The line
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5fc12a5d8aaa3e96d9eca419334f91e
https://doi.org/10.1016/j.chroma.2004.12.093
https://doi.org/10.1016/j.chroma.2004.12.093
Autor:
M. V. Kopyshev, E. F. Litvin, V. Z. Sharf, M. B. Nikishina, L. M. Kozlova, D. V. Gurylev, Ivan I. Vorontsov, Yu. M. Atroshchenko, I. V. Shakhkel'dyan, N. A. Troitskii, E. N. Alifanova
Publikováno v:
Russian Journal of Organic Chemistry. 40:255-260
During catalytic reduction with hydrogen on nickel of a series of 3-substituted 1,5-dinitro-3-azabicyclo-[3.3.1]non-6-enes alongside nitro groups reduction occurred also hydrogenation of the double bond. New diamines of the 3-azabicyclo[3.3.1]nonane
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f4af4415da54d23a6bae92edefb1994
https://doi.org/10.1023/b:rujo.0000034950.28394.e0
https://doi.org/10.1023/b:rujo.0000034950.28394.e0
Autor:
A.P. Kaplun, V. I. Shvets, E L Surkova, A. V. Symon, N. K. Vlasenkova, G. K. Gerasimova, E F Litvin, L M Kozlova, Le Bang Shon
Publikováno v:
Russian Journal of Bioorganic Chemistry. 29:185-189
Two methods of obtaining of 3 alpha-betulinic acid and related compounds from their 3 beta-epimers were studied: the reaction of bimolecular substitution and the stereoselective reduction of 3-ketoderivatives. The substitution of acyloxy by formyloxy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e91e1eea81b3cfb5bd024c8aa1311865
https://doi.org/10.1023/a:1023220701797
https://doi.org/10.1023/a:1023220701797
Autor:
S. N. Tandura, Elena V. Shuvalova, S. P. Kolesnikov, A. N. Shumsky, E. F. Litvin, L. M. Kozlova, V. Z. Sharf
Publikováno v:
Russian Chemical Bulletin. 50:1014-1022
The assignment of the signals for the H and C atoms of four diastereomers (without their separation) of 2-(1-aminoethyl)bicyclo[2.2.1]heptane (1) and its hydrochloride (2) (the antiviral drug deitiforin) was performed for the first time by two-dimens
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ad467c6661f74835cb9117547e83462
https://doi.org/10.1023/a:1011313117695
https://doi.org/10.1023/a:1011313117695
Autor:
Alexander A. Greish, Yu. A. Korolev, M. V. Kopyshev, Leonid M. Kustov, L. M. Kozlova, E. F. Litvin
Publikováno v:
Catalysis in Industry. 2:287-289
Glycerol dehydroxylation on a Raney cobalt catalyst in hydrogen was studied. It was found that with an increase in temperature from 140 to 200°C at a hydrogen pressure of 30 MPa, glycerol conversion increases from 14 to 97%. The glycerol is complete
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0815161f4f77b64392f0f3f817be9f19
https://doi.org/10.1134/s2070050410030141
https://doi.org/10.1134/s2070050410030141
Publikováno v:
Doklady Physical Chemistry. 398:223-225
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b3e3ecfd99d63cec39b3e95cc8f730a
https://doi.org/10.1023/b:dopc.0000041492.54540.74
https://doi.org/10.1023/b:dopc.0000041492.54540.74
Publikováno v:
Russian Chemical Bulletin. 42:1200-1203
It has been shown that depending on the catalyst and the solvent used, during the conversion of dibenzyl ether to toluene hydrogenolysis of C-O ether bonds, dehydrogenation and hydrogenolysis of benzyl alcohol formed, hydrogenation and decarbonylatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b71ba60718d03867031f0f552f9cce3e
https://doi.org/10.1007/bf00702006
https://doi.org/10.1007/bf00702006
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54b1684715162f972c4e480258f99e8b
https://doi.org/10.1002/chin.199252100
https://doi.org/10.1002/chin.199252100
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9d4369260be080a6161dee06646f8b1
https://doi.org/10.1002/chin.199431074
https://doi.org/10.1002/chin.199431074
Publikováno v:
ChemInform. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f9aa24791381986d620b47a74553034
https://doi.org/10.1002/chin.199608094
https://doi.org/10.1002/chin.199608094