Zobrazeno 1 - 10
of 73
pro vyhledávání: '"R. V. Kaberdin"'
Autor:
R. V. Kaberdin, Vladimir I. Potkin
Publikováno v:
Chemistry of Heterocyclic Compounds. 43:1493-1511
Published information on methods for the production of benzazetines and their dehydro derivatives (benzazetes) and their chemical transformations is reviewed and analyzed. It was noted that benzazetines with an unsubstituted NH group are unstable and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5dc714a2e37dd21689068fc4988a3e70
https://doi.org/10.1007/s10593-007-0233-4
https://doi.org/10.1007/s10593-007-0233-4
Publikováno v:
Russian Journal of Organic Chemistry. 43:1617-1621
Bromination of 3,4,4-trichlorobut-3-enoic acid in boiling carbon tetrachloride led to the formation of 2-bromo-3,4,4-trichlorobut-3-enoic acid as a result of replacement of hydrogen in the CH2 group. The reaction at 40°C involved the double C=C bond
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2d47e2f7d3145eda2c241946399f0bfa
https://doi.org/10.1134/s107042800711005x
https://doi.org/10.1134/s107042800711005x
Publikováno v:
Russian Journal of Organic Chemistry. 43:587-590
Butane-, phenylmethane-, and benzenethiols reacted with 4,5-dichloro-3-trichloromethyl-1,2-thiazole in the presence of sodium ethoxide to give the corresponding 5-alkyl(aryl)sulfanyl-4-chloro-3-trichloromethyl-1,2-thiazoles. The reaction of 4,5-dichl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7115eebefa11faf00342f13b6ef14de9
https://doi.org/10.1134/s1070428007040161
https://doi.org/10.1134/s1070428007040161
Publikováno v:
Russian Journal of Organic Chemistry. 42:1481-1485
The reaction of 1-aryl-3,4,4-trichlorobut-3-en-1-ones with semicarbazide hydrochloride in the presence of sodium acetate is accompanied by prototropic allylic rearrangement, leading to the formation of two isomeric products, semicarbazones of the ini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90d0ea57d5cbd84c6317820c881bdeb5
https://doi.org/10.1134/s1070428006100149
https://doi.org/10.1134/s1070428006100149
Publikováno v:
Russian Journal of Organic Chemistry. 40:1146-1150
3-Aryl-5-methylenehydroxyiminoisoxazoles were synthesized by reaction of 1-aryl-3,4,4-trichloro-3-buten-1-ones with hydroxylamine. Reactions of ketones with hydrazine provided pyrazole structures; therewith two pyrazole molecules underwent “couplin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f5fbe0de2253239077114c8af36959f
https://doi.org/10.1023/b:rujo.0000045896.42146.ad
https://doi.org/10.1023/b:rujo.0000045896.42146.ad
Publikováno v:
Russian Journal of Organic Chemistry. 40:729-732
Nitration of 4-alkoxy (Alk = Me, Et)-2-(1-nitro-2,3,3-trichloro-2-propenylidene)benzazetines with anhydrous HNO3 in glacial acetic acid afforded the corresponding 4-alkoxy-3-nitro-2-(1-nitro-2,3,3-trichloro-2-propenylidene)benzazetines. Reaction of c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7562098c35e5e1d9659f26fb9dc16dc
https://doi.org/10.1023/b:rujo.0000043722.09128.17
https://doi.org/10.1023/b:rujo.0000043722.09128.17
Autor:
A. V. Bazhanov, E. A. Dikusar, Vladimir I. Potkin, R. V. Kaberdin, Sergey K. Petkevich, N. V. Kovganko, N. G. Kozlov
Publikováno v:
Chemistry of Natural Compounds. 40:230-234
Previously unknown (Z)-3,4,4,4-tetrachlorobut-2-enoates 1b-20b were prepared in 77-88% yields by reaction in the presence of pyridine of 3,3,4,4,4-pentachlorobutanoic acid chloride with cetyl alcohol (1a), terpenols and terpenone oximes (2a-13a), ste
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::05b22c6075553a69341343c146f43ad1
https://doi.org/10.1023/b:conc.0000039130.83796.88
https://doi.org/10.1023/b:conc.0000039130.83796.88
Publikováno v:
Russian Journal of General Chemistry. 74:578-581
(Z)-2-Naphthylacetylene was synthesized by the reaction of (Z)-3-(2-naphthyl)-3-chloropropenal (prepared from 2-acetylnaphthalene) with aqueous NaOH in dioxane. The reactions of 2-naphthylacetylene with CuCl, [Ag(NH3)2]NO3, and K2[HgI4] gave copper,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::94464334d793191374503167d03a27a6
https://doi.org/10.1023/b:rugc.0000031860.91216.62
https://doi.org/10.1023/b:rugc.0000031860.91216.62
Autor:
Sergey K. Petkevich, Vladimir I. Potkin, A. P. Yuvchenko, E. A. Dikusar, R. V. Kaberdin, K. L. Moiseichuk, P. V. Kurman
Publikováno v:
Russian Journal of General Chemistry. 74:586-593
Substituted amides and esters of 3,4,4-trichloro-3-butenoic acid were prepared by reactions of its chloride with appropriate amines and alcohols. Treatment of 3,4,4-trichloro-3-butenomorpholide and tert-butyl 3,4,4-trichloro-3-butenoate results in nu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::231de74d408803299fc778adc789cc20
https://doi.org/10.1023/b:rugc.0000031862.88263.de
https://doi.org/10.1023/b:rugc.0000031862.88263.de
Autor:
N. V. Kovganko, R. V. Kaberdin, N. G. Kozlov, Vladimir I. Potkin, E. A. Dikusar, N. I. Nechai
Publikováno v:
Chemistry of Natural Compounds. 39:186-190
Previously unknown esters 1b-14b were prepared by reaction of cetyl alcohol 1a, terpene alcohols 2a-6a, sterols 7a-11a, and plant phenols 12a-14a with 4,5-dichloroisothiazol-3-carboxylic acid chloride.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc1435b6b842d7a1e490191653e4f3ac
https://doi.org/10.1023/a:1024865931052
https://doi.org/10.1023/a:1024865931052