Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Klimenko Galina R"'
Publikováno v:
Russian Journal of Organic Chemistry. 50:219-224
Transformations of oxazolidine derivatives synthesized from industrially produced amino alcohols, aldehydes, and ketones under basic or acidic catalysis lead to the formation of N-alkyl- and N-(hydroxyalkyl)-substituted pyrroles in 19-81% yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ae0d1c21262e4bac2565694d3b062cd
https://doi.org/10.1134/s1070428014020134
https://doi.org/10.1134/s1070428014020134
Publikováno v:
Russian Journal of Organic Chemistry. 47:1817-1822
2- and 4-Fluorobenzaldehydes reacted with amino alcohol vinyl ethers to give Schiff bases, oxazolidines, and imidazolidines containing a vinyloxy group. The products attract interest as potential biologically active compounds.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::41021d5c740dfe86efd9686bbedc20cb
https://doi.org/10.1134/s1070428011120074
https://doi.org/10.1134/s1070428011120074
Autor:
E. V. Bragin, Klimenko Galina R, V. V. Stankevich, Kukharev Boris F, V. K. Stankevich, N. A. Lobanova
Publikováno v:
Russian Journal of Organic Chemistry. 46:491-494
Reactions of N-(2-vinyloxyalkyl)ethane-1,2-diamines with 1,3-dicarbonyl compounds gave the corresponding enamino ketones in almost quantitative yield (98–99%).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e0dfe3bb1e6cbee5c7cac2de5a241e9
https://doi.org/10.1134/s1070428010040068
https://doi.org/10.1134/s1070428010040068
Autor:
E. V. Bragin, Klimenko Galina R, N. A. Lobanova, V. K. Stankevich, V. V. Stankevich, Kukharev Boris F
Publikováno v:
Russian Journal of Organic Chemistry. 46:495-498
Condensation of N-(2-vinyloxyethyl)ethane-1,2-diamine with aromatic aldehydes gave mixtures of 2-aryl-1-(2-vinyloxyethyl)imidazolidines and N-arylmethylidene-N′-(2-vinyloxyethyl)ethane-1,2-diamines in an overall yield of 79–84%, while analogous c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dff1e8157c318c22d60828d223b3682a
https://doi.org/10.1134/s107042801004007x
https://doi.org/10.1134/s107042801004007x
Publikováno v:
Russian Journal of Organic Chemistry. 45:22-25
The kinetic and thermodynamic parameters of the Hg(II)-catalyzed cyclization of N-phenyl-2-vinyloxyethanamine indicated that the first reaction step is reversible coordination of mercury at the vinyloxy group, followed by closure of mercurated oxazol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2726ee673fcb7a7f1c2caa0cf4ffe9f6
https://doi.org/10.1134/s1070428009010035
https://doi.org/10.1134/s1070428009010035
Publikováno v:
Russian Journal of Organic Chemistry. 45:1420-1422
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ae96e3e92ae98e51a4bc39c4e48e482
https://doi.org/10.1134/s1070428009090218
https://doi.org/10.1134/s1070428009090218
Publikováno v:
Russian Journal of Organic Chemistry. 44:1494-1496
Base-catalyzed reaction of 2-hydroxybenzaldehyde with 2-{[2-(vinyloxy)ethoxy]methyl}oxirane gave 2-{2-hydroxy-3-[2-(vinyloxy)ethoxy]propoxy}benzaldehyde in 42% yield, and subsequent condensations of the product with thiosemicarbazide and primary alip
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00364c5fc1a98e73e8e7dba1931d7e53
https://doi.org/10.1134/s1070428008100151
https://doi.org/10.1134/s1070428008100151
Synthesis of O-[2-hydroxy-3-(vinyloxy)propyl]oximes and O-[(2-methyl-1,3-dioxolan-4-yl)methyl]oximes
Publikováno v:
Russian Journal of Organic Chemistry. 43:181-183
By oximes reaction with glycidyl vinyl ether O-[2-hydroxy-3-(vinyloxy)propyl]oximes of ketones and acetaldehyde were synthesized in 54–72% yield, and by acid catalysis the compounds were converted into O-[(2-methyl-1,3-dioxolan-4-yl)methyl]oximes i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21ad4874b40f4e301e75ebc8a79b4bac
https://doi.org/10.1134/s1070428007020042
https://doi.org/10.1134/s1070428007020042
Publikováno v:
Russian Chemical Bulletin. 46:2113-2116
N-(Vinyloxyalkyl)enaminoketones were obtained by the condensation of vinyloxyalkylamines with acetylacetone or ethyl acetoacetate. Their subsequent reactions with 1,4-benzoquinone produce the corresponding 5-hydroxy-2-methyl-N-(2-vinyloxyalkyl)indole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e702f91486c32c40de6c57253bc5cda7
https://doi.org/10.1007/bf02495263
https://doi.org/10.1007/bf02495263
Publikováno v:
Russian Chemical Reviews. 64:523-540
The results of studies on the methods of synthesis and properties of the vinyl ethers of aminoalcohols are surveyed and described systematically. Their principal applications are considered. The bibliography includes 265 references.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa0ee254f632ab27d7fff1d3c04f2a65
https://doi.org/10.1070/rc1995v064n06abeh000163
https://doi.org/10.1070/rc1995v064n06abeh000163