Zobrazeno 1 - 10
of 41
pro vyhledávání: '"A. I. Deiko"'
Publikováno v:
Russian Journal of General Chemistry. 77:25-35
Diene condensations of 2-nitro-and 2-bromo-2-nitroethenylphosphonates with 2,3-dimethyl-1,3-butadiene, as well as with 2,4-dihydro-and 3-methyl-2,4-dihydrothiophene 1,1-dioxides that generate 1,3-butadiene and isoprene under the reaction conditions w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::926846bc3700b4889975b8b709785d78
https://doi.org/10.1134/s1070363207010045
https://doi.org/10.1134/s1070363207010045
Publikováno v:
Russian Journal of General Chemistry. 75:1750-1756
Investigation of the reactions of phosphorylated 2-nitro- and 2-bromo-2-nitroethenes with furan showed that bis(2-chloroethyl) 2-nitroethenylphosphonate reacts with this heterocycle according to the pathway of diene condensation, while in the case of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55ee5f456dbbb6709dc03f19b3c84c15
https://doi.org/10.1007/s11176-005-0504-7
https://doi.org/10.1007/s11176-005-0504-7
Publikováno v:
Russian Journal of General Chemistry. 75:1045-1049
Specific features of the reactions of bis(chloroethyl) 2-nitro- and 2-bromo-2-nitroethenylphosphonates with 1,3-cyclohexadiene were studied. It was found that the reaction with 2-nitroethenylphosphonate occurs stereoselectively and provides bis(2-chl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::636b4e551768555a10bb1af3a7badb7a
https://doi.org/10.1007/s11176-005-0365-0
https://doi.org/10.1007/s11176-005-0365-0
Publikováno v:
Russian Journal of General Chemistry. 75:689-693
Bis(2-chloroethyl) 2-nitro- and 2-bromo-2-nitroethenylphosphonates react with anthracene along two competing pathways: [4+2] cycloaddition and electrophilic substitution; in the case of the bromo derivative, the resulting products undergo dehydrobrom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e3f486b82d4c2ec285fa752567851ab
https://doi.org/10.1007/s11176-005-0299-6
https://doi.org/10.1007/s11176-005-0299-6
Autor:
V. M. Berestovitskaya, L. I. Deiko, Z. M. Sarkisyan, A. G. Gubaidullin, G. A. Berkova, I. A. Litvinov, G. R. Fattakhova, Ya. A. Vereshchagina, Eleonora A. Ishmaeva, S. V. Makarenko
Publikováno v:
Russian Journal of General Chemistry. 74:110-119
A method was developed for preparing first representatives of phosphorylated nitrovinylindoles, bis(2-chloroethyl) 1-(indol-3-yl)- and bis(2-chloroethyl) 1-(1-alkylindol-3-yl)-2-nitroethenylphosphonates, and the structures of these compounds were stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b6e08371c35565262b31e7adb72d926
https://doi.org/10.1023/b:rugc.0000025178.22976.6b
https://doi.org/10.1023/b:rugc.0000025178.22976.6b
Publikováno v:
Russian Journal of General Chemistry. 72:86-90
Hydrolysis of substituted cyclopropane amino acids was performed. Free and partially substituted Z and E isomers of cyclopropane analogs of aspartic and adipic acids were obtained.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c885f06d32a1e891bd5c8ee8b206daed
https://doi.org/10.1023/a:1015301513947
https://doi.org/10.1023/a:1015301513947
Publikováno v:
Russian Journal of General Chemistry. 72:272-275
Cyclopropane analogs of aspartic and adipic acids were prepared by catalytic cyclopropanation of dehydro amino acid derivatives with alkyl diazoacetates in the presence of catalyst (dirhodium tetraacetate).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c68cb628b6c97e5e9a30deef73b0e35c
https://doi.org/10.1023/a:1015438005249
https://doi.org/10.1023/a:1015438005249
Publikováno v:
Russian Journal of General Chemistry. 72:460-463
Thermal decomposition of substituted Δ1- and Δ2-pyrazolines was used to obtain cyclopropane derivatives of aspartic and adipic acids.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::48f38ef91e9f0a7bd17fd12a8a343ba9
https://doi.org/10.1023/a:1015468306583
https://doi.org/10.1023/a:1015468306583
Publikováno v:
Russian Journal of General Chemistry. 76:153-155
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a36750212e7d774837d22d4df72a7d6a
https://doi.org/10.1134/s1070363206010294
https://doi.org/10.1134/s1070363206010294
Publikováno v:
Russian Journal of General Chemistry. 75:1495-1497
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d56a2f02785db5d01bd8f0aa045aef76
https://doi.org/10.1007/s11176-005-0453-1
https://doi.org/10.1007/s11176-005-0453-1