Zobrazeno 1 - 10
of 42
pro vyhledávání: '"L. F. Chertanova"'
Autor:
F. S. Zarudii, E.E. Shultz, V. A. Davydova, Popov Vg, L. F. Chertanova, Tolstikov Genrikh A, T. G. Tolstikova, Leonid V. Spirikhin, T. Sh. Mukhametyanova, A. A. Gazikasheva, D. N. Lazareva
Publikováno v:
Pharmaceutical Chemistry Journal. 26:834-842
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5cc7ae5f2955ede9484991203657d6b8
https://doi.org/10.1007/bf00767655
https://doi.org/10.1007/bf00767655
Autor:
N. G. Gazetdinova, O. A. Erastov, A. A. Karasik, O. K. Pozdeev, L. F. Chertanova, Zemfira A. Bredikhina, G. Kh. Gil'manova
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::062754d7034e0f28e0ba76867599ad45
https://doi.org/10.1002/chin.199115217
https://doi.org/10.1002/chin.199115217
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7508d0b6c4067399a3a4a3627818baed
https://doi.org/10.1002/chin.199114163
https://doi.org/10.1002/chin.199114163
Publikováno v:
ChemInform. 22
C-Trimethylsiloxy substituted phosphaalkene 1 reacts exothermically with diphenylchloroborane. The expected spontaneous 1,3-eIimination of trimethylsiloxydiphenylborane took place to give phosphaalkyne 3 in 1–2% yield only. The symmetrization of in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0a2bd9089ac23795549502e338b591e
https://doi.org/10.1002/chin.199119226
https://doi.org/10.1002/chin.199119226
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f66895936b1dc69b41ec913234dc0fa
https://doi.org/10.1002/chin.199206217
https://doi.org/10.1002/chin.199206217
Autor:
Oleg A. Rakitin, N. V. Obruchnikova, A. A. Gazikasheva, Lenor I. Khmel’nitskii, L. F. Chertanova, V. A. Ogurtsov
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c364cf4c50336a64267028376c64eeb1
https://doi.org/10.1002/chin.199136190
https://doi.org/10.1002/chin.199136190
Autor:
A. A. Gazikasheva, Igor A. Litvinov, M. A. Pudovik, L. F. Chertanova, G. S. Stepanov, R. M. Kamalov, Rashid Z. Musin
Publikováno v:
ChemInform. 23
Reactions of hexaethyltriaminophosphine and tetraethyldiaminophenylphosphine with alkyl thiocyanates have been found to proceed in an unusual way and to give rise to the appropriate aminophosphine sulfides, alkyl cyanides, dialkyl sulfides and disulf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d8955caea108f48b1d8fe6edd09c9f5
https://doi.org/10.1002/chin.199238207
https://doi.org/10.1002/chin.199238207
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3978f7ebd4a3fcfce2a8e593302f6e79
https://doi.org/10.1002/chin.199244078
https://doi.org/10.1002/chin.199244078
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::150810509bcc64be5eaf4c13ac755689
https://doi.org/10.1002/chin.199234224
https://doi.org/10.1002/chin.199234224
Autor:
L. F. Chertanova, A. N. Pudovik, M. A. Pudovik, A. A. Gazikasheva, R. M. Kamalov, G. S. Stepanov
Publikováno v:
ChemInform. 24
Reactions of phenyl isothiocyanato(di)chloro-methyl(thio)phosphonates (1) with thiols in the presence of a base give rise to 2-alkylthio-4,5-dihydro-4-oxo(thioxo)-4-phenoxy-1,3,4-thiazaphospholes (5). Some of these compounds can also be obtained by a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83aaf5c31751fbf3a81410ccd019b282
https://doi.org/10.1002/chin.199343190
https://doi.org/10.1002/chin.199343190