Zobrazeno 1 - 9
of 9
pro vyhledávání: '"D. O. Samultsev"'
Publikováno v:
Russian Chemical Bulletin. 64:2756-2762
13C NMR shielding constants (chemical shifts) of iodomethanes were calculated within the framework of the full four-component relativistic Dirac—Coulomb scheme. As the number of iodine atoms in the molecule increases, the relativistic counterpart o
Publikováno v:
Russian Journal of Organic Chemistry. 49:734-738
By reactions of 3-alkenyl-5-chloropyrazoles with appropriate dichalcogenols the fi rst specimens were obtained of previously unknown 3,3’-linearly linked bispyrazoles containing in the alkyl chain of the linker two heteroatoms, sulfur or selenium.
Publikováno v:
Russian Journal of Organic Chemistry. 47:1870-1873
First representatives of bis-2-chloro- and 2,2-dichlorovinyl ketones, 1,10-dichlorodeca-1,9-diene-3,8-dione and 1,1,10,10-tetrachlorodeca-1,9-diene-3,8-dione, were synthesized by reaction of hexanedioyl dichloride with acetylene and 1,1-dichloroethen
Publikováno v:
ChemInform. 44
By reactions of 3-alkenyl-5-chloropyrazoles with appropriate dichalcogenols the fi rst specimens were obtained of previously unknown 3,3’-linearly linked bispyrazoles containing in the alkyl chain of the linker two heteroatoms, sulfur or selenium.
Publikováno v:
ChemInform. 44
Autor:
A. I. Albanov, D. O. Samultsev, Galina G. Levkovskaya, Elena V. Rudyakova, V. V. Kobelevskaya
Publikováno v:
ChemInform. 42
Autor:
D. O. Samultsev, Khanh Ha, Galina G. Levkovskaya, Igor B. Rozentsveig, Valentina A. Kobelevskaya, Elena V. Rudyakova
Publikováno v:
ChemInform. 42
Synthesis of hard-to-reach 5-chloro-3-alkenylpyrazoles was developed via heterocyclization of alkyl-, benzyl- or dialkylhydrazines with 1,1-dichloro-4-halo-1-alken-3-ones obtained from haloacyl chlorides and vinylidene chloride. The reaction process
Publikováno v:
Russian Journal of Organic Chemistry. 48:1388-1389
Autor:
D. O. Samultsev, Elena V. Rudyakova, A. I. Albanov, V. V. Kobelevskaya, Galina G. Levkovskaya
Publikováno v:
Russian Journal of Organic Chemistry. 47:302-303