Zobrazeno 1 - 10
of 18
pro vyhledávání: '"T. N. Polyanskaya"'
Autor:
V. M. Berezovskii, T. M. Filippova, I. G. Suchkova, S. I. Peretokina, S. D. Mikhno, T. N. Polyanskaya
Publikováno v:
Chemistry of Heterocyclic Compounds. 14:1315-1319
It is shown that acrolein adds to the 4 position (rather than to the 2 position) of 4-benzamido-3-oxothiophan under the influence of catalysts with basic character; the aldehyde group of the intermediate compound reacts with the amino group (if the r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1f39eb53729436de3bb146c4614e039
https://doi.org/10.1007/bf00487397
https://doi.org/10.1007/bf00487397
Publikováno v:
Chemistry of Heterocyclic Compounds. 6:1501-1505
The reduction of 4-benzoylamino- and 4-carbethoxyamino-3-ketothiophanes proceeds stereospecifically to form only trans-4-benzoylamino- and trans-4-carbethoxyamino-3-hydroxythiophanes, respectively, from which trans-4-amino-3-hydroxythiophane is obtai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81f7ce5df749f56dac1dc896214badaa
https://doi.org/10.1007/bf00522566
https://doi.org/10.1007/bf00522566
Autor:
I. M. Kustanovich, T. M. Filippova, T. N. Polyanskaya, V. M. Berezovskii, N. S. Kulachkina, S. D. Mikhno
Publikováno v:
Chemistry of Heterocyclic Compounds. 8:813-817
The stereospecific synthesis of the four possible isomers of 4-benzamido-3-hydroxy-2-(δ-carbomethoxybutyl)thiophan (III–VI) was accomplished from 4-benzamido-3-oxo-2-(δ-carbomethoxybutylidene)thiophan (I) using the stereospecificity of the reduct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dcb092b2ff6fd3c396de67ca5cd42b5e
https://doi.org/10.1007/bf00475209
https://doi.org/10.1007/bf00475209
Autor:
I. M. Kustanovich, S. D. Mikhno, V. V. Mishchenko, T. M. Filippova, V. M. Berezovskii, N. S. Kulachkina, I. K. Shmyrev, T. N. Polyanskaya
Publikováno v:
Chemistry of Heterocyclic Compounds. 8:687-692
The structure of stereoisomeric 4-benzamido-3-hydroxy-2-carbomethoxythiophans was established by means of PMR and IR spectroscopy. The inversion of the trans,trans-isomer to the cis,trans-isomer was detected and studied. The inversion during the acti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::261615d4bac72640081ce88455d5aa48
https://doi.org/10.1007/bf00487459
https://doi.org/10.1007/bf00487459
Publikováno v:
Chemistry of Heterocyclic Compounds. 10:916-918
Condensation of 4-ethoxycarbonylamino-3-oxothiophan with methyl γ-formylbutyrate gives 4-ethoxycarbonylamino-3-oxo-2-(δ-methoxycarbonlybutyl)thiophan, its oxime, and r-4-eth-oxycarbonylamino-t-3-hydroxy-c-2-(δ-methoxycarbonylbutyl)thiophan.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70b8bf38f3eb92e7c8a2c764de2404c1
https://doi.org/10.1007/bf00487109
https://doi.org/10.1007/bf00487109
Publikováno v:
Metallurgist. 13:655-657
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c343f63406e69de5f2efa65b6bdc3c5
https://doi.org/10.1007/bf00734629
https://doi.org/10.1007/bf00734629
Publikováno v:
Chemistry of Heterocyclic Compounds. 9:161-163
trans-4-Benzamido-3-hydroxy-2-(4-carbomethoxybutylidene)thiophan (I) was prototropically isomerized in the presence of hydrogen chloride. It is shown that the two possible isomers cis- and trans-4-benzamido-3-oxo-2-(4-carbomethoxybutyl)thiophan — a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d3d4611eb8bf16f48b0f9658d198a757
https://doi.org/10.1007/bf00569151
https://doi.org/10.1007/bf00569151
Autor:
I. F. Ermak, É. S. Glikman, V. V. Sementovskii, T. N. Polyanskaya, V. D. Gladush, B. P. Bel'gol'skii
Publikováno v:
Metallurgist. 15:528-530
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64acb4e446a5bcfb7ef36b1cb76606c9
https://doi.org/10.1007/bf01152509
https://doi.org/10.1007/bf01152509
Publikováno v:
Chemischer Informationsdienst. 5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0a15115659ff29e3a89b75c58e6fb3a
https://doi.org/10.1002/chin.197449263
https://doi.org/10.1002/chin.197449263
Publikováno v:
Chemischer Informationsdienst. 4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::594a56438f9d806818c9ccc009e84e27
https://doi.org/10.1002/chin.197322265
https://doi.org/10.1002/chin.197322265