Zobrazeno 1 - 10
of 153
pro vyhledávání: '"Rafael A. Cherkasov"'
Autor:
Ilyas S. Nizamov, Ramazan Z. Salikhov, Ilnar D. Nizamov, Elvira S. Batyeva, Rafael A. Cherkasov
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 197:535-537
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::efa2693450e8fa9fd07fabb179538643
https://doi.org/10.1080/10426507.2021.2011876
https://doi.org/10.1080/10426507.2021.2011876
Publikováno v:
ARKIVOC, Vol 2004, Iss 1, Pp 130-137 (2004)
Externí odkaz:
https://doaj.org/article/e78f5b34655a4f428c4d2c4c3296b3cf
Autor:
Helene Wahe, Joseph T. Mbafor, Augustin E. Nkengfack, Zacharias T. Fomum, Rafael A. Cherkasov, Olov Sterner, Dietrich Doepp
Publikováno v:
ARKIVOC, Vol 2003, Iss 15, Pp 107-114 (2004)
Externí odkaz:
https://doaj.org/article/b1bd29b086f042af8deda84e90441fbf
Autor:
Helene Wahe, Peter F. Asobo, Rafael A. Cherkasov, Augustin E. Nkengfack, Gabriel N. Folefoc, Zacharias T. Fomum, Dietrich Doepp
Publikováno v:
ARKIVOC, Vol 2003, Iss 14, Pp 170-177 (2003)
Externí odkaz:
https://doaj.org/article/1eab3c2e5bd84fb1a17c07dc4edb7b4a
Autor:
Irina V. Galkina, Yuliya V. Bakhtiyarova, Marina P. Shulaeva, Oskar K. Pozdeev, Svetlana N. Egorova, Rafael A. Cherkasov, Vladimir I. Galkin
Publikováno v:
Journal of Chemistry, Vol 2013 (2013)
The purpose of the present study was to investigate the antibacterial activity of fifteen novel nanosized alkyl esters of carboxylate phosphabetaine: β-(carboxyalkyl)ethyltriphenylphosphonium bromides 4–8, β-(carboxyalkyl)-β-methylethyltriphenyl
Externí odkaz:
https://doaj.org/article/6aa096573ed7418c90dae59439842b3f
Autor:
Rafael A. Cherkasov, Il'yas S. Nizamov, Lyubov A. Al'metkina, Yevgeniy N. Nikitin, Gulnara T. Gabdullina, I. D. Nizamov
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 185:732-742
A method of synthesizing arylbisdithiophosphonic acids was developed by the reaction of 2,4-diaryl 1,3,2,4-dithiadiphosphetane-2,4-disulfides with tri(ethylene glycol) and 1,4-butandiol in anhydrous benzene suspension under mild conditions. The arylb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b47baf3bc34068c67b9609944aacdcc0
https://doi.org/10.1080/10426500902930142
https://doi.org/10.1080/10426500902930142
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 184:865-871
The reaction of 1,2-diaminoethane with vinylphosphonate occurs as the addition of the amino group to the β -carbon atom of the unsaturated substrate to give 1:1 and 1:2 adducts. The nucleophilic addition of 2-aminoethanol at the β -position of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9894a9f44823490865b979f8442b5fb
https://doi.org/10.1080/10426500802715577
https://doi.org/10.1080/10426500802715577
Autor:
Igor A. Litvinov, Boris N. Solomonov, Rafael A. Cherkasov, Nikolay A. Mironov, Vasiliy V. Brusko, Maria G. Babashkina, Nail G. Zabirov, Damir A. Safin, Felix D. Sokolov, Dmitry B. Krivolapov
Publikováno v:
Polyhedron. 26:1550-1560
For N -(thio)phosphorylthioureas of the common formula RC(S)NHP(X)(O i Pr) 2 HL I (R = N -(4′-aminobenzo-15-crown-5), X = S), HL II (R = N -(4′-aminobenzo-15-crown-5), X = O), HL III (R = PhNH, X = S), HL IV (R = PhNH, X = O), and ( N , N ′-bis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::41d7e785e3fb865b0c9b1376718f6556
https://doi.org/10.1016/j.poly.2006.12.024
https://doi.org/10.1016/j.poly.2006.12.024
Autor:
Felix D. Sokolov, Igor A. Litvinov, Damir A. Safin, Robert C. Luckay, Dmitry B. Krivolapov, Nail G. Zabirov, Rafael A. Cherkasov, Vasiliy V. Brusko
Publikováno v:
Polyhedron. 25:3330-3336
Reaction of the potassium salts of N-thioacylamidophosphates RC(S)NHP(O)(OPri)2 (R = Ph, PhNH, p-MeOPhNH, p-BrPhNH, iPrNH, tBuNH, Et2N, c-C5H10N, c-OC4H8N, c-C5H11NH) with Co(II) cation in aqueous EtOH leads to the complexes of Co(L-O,S)2 type struct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::94d66f95db7a5dc09c1d35a467bcea7a
https://doi.org/10.1016/j.poly.2006.06.005
https://doi.org/10.1016/j.poly.2006.06.005
Autor:
G. Kh. Nuriazdanova, N. S. Krasnova, Olga A. Mostovaya, N. G. Khusainova, E. A. Berdnikov, Rafael A. Cherkasov, Airat R. Garifzyanov, Vladimir I. Galkin
Publikováno v:
Russian Journal of Organic Chemistry. 41:1481-1484
New and previously known β-aminoethylphosphonates were synthesized by addition of primary and secondary amines to vinylphosphonates, and their IR and NMR spectra were examined. Diethyl 2-diethylaminoethylphosphonate and diethyl 2-morpholinoethylphos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::068831507229730b715f0869a1dd3469
https://doi.org/10.1007/s11178-005-0370-0
https://doi.org/10.1007/s11178-005-0370-0