Zobrazeno 1 - 10
of 28
pro vyhledávání: '"S. V. Shorshnev"'
Publikováno v:
Pharmaceutical Chemistry Journal. 38:197-205
Autor:
Detlef Gabel, S. V. Shorshnev, N. A. Klyuev, U. Doerfler, K. Bauer, Yu. A. Azev, Mohamed E. El-Zaria
Publikováno v:
Pharmaceutical Chemistry Journal. 37:238-242
Publikováno v:
Pharmaceutical Chemistry Journal. 36:146-150
Autor:
Yu. A. Azev, Oleg N. Chupakhin, S. V. Shorshnev, O. L. Guselnikova, Vladimir L. Rusinov, I. P. Loginova
Publikováno v:
Mendeleev Communications. 4:104-107
The reaction of 2,4-diazido- s -triazines 1 with an equimolar amount or a two-fold molar excess of ethyl cyanoacetate in the presence of triethylamine in DMF affords the corresponding mono- 2 or diamino derivatives of s-triazine 3 ; on heating 2,4-di
Publikováno v:
ChemInform. 22
Autor:
Valerii N. Charushin, Elizaveta Tsoi, S. V. Shorshnev, Yu. A. Azev, S. G. Alexeev, Oleg N. Chupakhin
Publikováno v:
ChemInform. 24
Reactions of 7-(X)-substituted ethyl 1-amino-4-oxo-1,4-dihydroquinoline-3-carboxylates (1a-c; X = F, Cl and 4-methylpiperazin-1-yl) with mono- and di-ketones have been studied. Treatment of 1a; X = F with cyclopentanone and cyclopentanone in acetic a
Publikováno v:
ChemInform. 24
Deprotonation of 1-alkyl-5-phenyl-1,2,4-triazinium salts by triethylamine results in the formation of azomethyne ylides which undergo a 1,3-dipolar cycloaddition reaction with diethyl acetylenedicarboxylate to yield pyrrolo[2,1- f ]1,2,4-triazines
Autor:
O. L. Guselnikova, Vladimir L. Rusinov, Yu. A. Azev, I. P. Loginova, S. V. Shorshnev, Oleg N. Chupakhin
Publikováno v:
ChemInform. 25
The reaction of 2,4-diazido- s -triazines 1 with an equimolar amount or a two-fold molar excess of ethyl cyanoacetate in the presence of triethylamine in DMF affords the corresponding mono- 2 or diamino derivatives of s-triazine 3 ; on heating 2,4-di
Publikováno v:
ChemInform. 27
Publikováno v:
Pharmaceutical Chemistry Journal. 26:641-644
In this work the 13C NMR spectra with complete suppression of spin--spin coupling of the carbon nuclei with protons were studied for progesterone (I), hydroxyprogesterone caproate (II), medroxyprogesterone acetate (III), acetomepregnenole (IV), pregn