Zobrazeno 1 - 10
of 41
pro vyhledávání: '"R. I. Kruglikova"'
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6056238e59fa865e7f6951569739077d
https://doi.org/10.1002/chin.199133123
https://doi.org/10.1002/chin.199133123
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::12273fa48d7dd87f49fe61e181a61b01
https://doi.org/10.1002/chin.199551085
https://doi.org/10.1002/chin.199551085
Autor:
O. V. Kharitonova, L. M. Yagupol'skii, R. I. Kruglikova, A. V. Bogolyubskii, S. M. Makin, B. M. Arshava
Publikováno v:
ChemInform. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da36f43be0eab2d8f728ca7b22495bef
https://doi.org/10.1002/chin.199040129
https://doi.org/10.1002/chin.199040129
Publikováno v:
ChemInform. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3877ce3565c4a16835beecec8bc11655
https://doi.org/10.1002/chin.199021286
https://doi.org/10.1002/chin.199021286
Publikováno v:
ChemInform. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32ab965da1ea46c09009b888dbc60c08
https://doi.org/10.1002/chin.199013147
https://doi.org/10.1002/chin.199013147
Autor:
L. N. Kralinina, R. I. Kruglikova
Publikováno v:
Chemistry of Heterocyclic Compounds. 8:792-795
A number of 2,6-dialkoxy-3-bromotetrahydropyrans were obtained by the electrochemical bromomethoxylation of 2-alkoxy-Δ5-dihydropyrans. An assumption regarding the stereo-specificity of the electrochemical and chemical bromoalkoxylation was stated on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7d6bcf570e45f465da5cad7bc4f6f2d4
https://doi.org/10.1007/bf00475203
https://doi.org/10.1007/bf00475203
Autor:
L. N. Kralinina, R. I. Kruglikova
Publikováno v:
Chemistry of Heterocyclic Compounds. 8:672-675
The reduction of 2,5-dimethoxytetrahydrofurans, 2,5-dimethoxydihydrofurans, 2,6-dialkoxytetrahydropyrans, and 2,6-dialkoxydihydropyrans with mixtures of LiAlH4 and AlCl3 with various component ratios (3∶1, 1∶1, and 1∶3) proceeds with ring openi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7347225cdf11d306ef5f579421f4ccc
https://doi.org/10.1007/bf00487455
https://doi.org/10.1007/bf00487455
Publikováno v:
Chemistry of Heterocyclic Compounds. 8:796-799
The oxidation of trans-2,6-diethoxy-Δ 3-dihydropyran with perbenzoic acid gave a mixture of stereoisomeric epoxides, from which one individual isomer was isolated. The configuration and conformation of the epoxide obtained was established by PMR spe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2607ea6f31fff05e513d003862363b5c
https://doi.org/10.1007/bf00475204
https://doi.org/10.1007/bf00475204
Publikováno v:
Chemistry of Heterocyclic Compounds. 6:290-292
The Grignard reaction with 2, 6-dialkoxytetrahydropyran and 2, 6-dialkoxy-5, 6-dihydro-2H-pyran has been studied. In both cases the reaction takes place with the opening of the pyran ring and the formation of alkoxy-substituted saturated or γ, δ-un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5703f0cfdd8cb60712dcff55ca34d93a
https://doi.org/10.1007/bf00471222
https://doi.org/10.1007/bf00471222
Autor:
R. I. Kruglikova, Z. F. Abramova
Publikováno v:
Chemischer Informationsdienst. 5
Die trans-Phenylallylamine (III) werden durch Kondensation von Cinnamylchlorid (I) mit den Aminen (II) dargestellt; beim Versuch einer partiellen Hydrierung entsprechender Phenylpropargylamine mit Na in NH3 erhalt man Phenylpropylamine.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6e743f61ca4bb8c01f77411ca2d451b
https://doi.org/10.1002/chin.197424236
https://doi.org/10.1002/chin.197424236