Zobrazeno 1 - 10
of 23
pro vyhledávání: '"G. S. Litvinenko"'
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59546fc4a12716d3f707b2ae0953b7f0
https://doi.org/10.1002/chin.199236174
https://doi.org/10.1002/chin.199236174
Autor:
G. S. Litvinenko, T. K. Iskakova
Publikováno v:
Chemistry of Heterocyclic Compounds. 27:859-863
Equilibration of stereoisomeric cyclic ethinylcarbinols, epimeric at the carbinol center, was conducted for the first time and it was shown that the equilibrium is shifted toward the equatorial alcohol (at 50‡C for 2e-methyl-4-hydroxy-4-phenylethin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65ca1d4d074fb6bdb9db648ea0f5b37b
https://doi.org/10.1007/bf00472286
https://doi.org/10.1007/bf00472286
Autor:
E. G. Yalovenko, G. S. Litvinenko
Publikováno v:
Chemistry of Heterocyclic Compounds. 26:53-57
The 13C NMR spectra of 5-keto- and 5a- and 5e-hydroxy-10-methyl- and 1,10-dimethyltrans-decahydroquinolines have been recorded and interpreted. The increments of the oxo and hydroxy groups in the 10-methyldecahydroquinoline and the isostructural 10-m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::668d9b0c9e72936569177b0f40159891
https://doi.org/10.1007/bf00506848
https://doi.org/10.1007/bf00506848
Publikováno v:
Chemistry of Heterocyclic Compounds. 24:906-914
It is shown that epimeric [with respect to the C(2) atom] 1-chloro-2-methyl-4-keto-trans-decahydroquinolines in an acidic medium undergo intermolecular monochlorination in the α position relatve to the carbonyl group with the formation of epimeric [
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b9643ca068f56dcba4b9424e867f5e8
https://doi.org/10.1007/bf00479348
https://doi.org/10.1007/bf00479348
Publikováno v:
Chemistry of Heterocyclic Compounds. 20:309-314
Three isomers of 1,2-dimethyldecahydroquinolin-5-ol and their acetates with cis and trans fusion of the rings and different orientations of the hydroxy and acyloxy groups were obtained. The correlation of the frequencies of the C-O, O-H, and N+-H str
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9822688328ffd1a6ca679c163d817038
https://doi.org/10.1007/bf00515646
https://doi.org/10.1007/bf00515646
Autor:
L. A. Voronenko, G. S. Litvinenko
Publikováno v:
Chemistry of Heterocyclic Compounds. 23:200-204
Reduction of 1-benzoyl-2α-methyl-4-oxo-cis-decahydroquinoline with sodium borohydride and sodium in alcohol has given 1-benzoyl-2α-methyl-4Β-hydroxy-cis-decahydroquinoline, which exists in the steroidal conformation with diaxial α, α′-substitu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5aea926935c0e1997abf8d251140323
https://doi.org/10.1007/bf00663862
https://doi.org/10.1007/bf00663862
Autor:
G. S. Litvinenko, L. A. Voronenko
Publikováno v:
Chemistry of Heterocyclic Compounds. 20:643-649
Epimeric (with respect to the methyl group) stereoisomers of 4-keto-2-methyl-1-chloro-trans-decahydroquinoline were obtained, and their transformations under the influence of triethylamine were investigated. It was shown that the direction of the tra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d66251a671be87a7bf98a2f541831757
https://doi.org/10.1007/bf00508674
https://doi.org/10.1007/bf00508674
Publikováno v:
Chemistry of Heterocyclic Compounds. 25:796-804
The isomers of 1-benzoyl-2,5-dimethyl-4-piperidone were obtained and equilibrated (89.8% cis ⇄ 10.2% trans isomer, preferred conformations 2a, 5e, and 2a, 5a). The position of the equilibrium between the isomers of 2,5-dimethyl-4-piperidone was det
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2189d5b8aac951473f7da296f6dcacae
https://doi.org/10.1007/bf00472753
https://doi.org/10.1007/bf00472753
Autor:
N. Yu. Kuz'mina, G. S. Litvinenko
Publikováno v:
Chemistry of Heterocyclic Compounds. 23:1211-1215
Isomers of 2-methyl- and 1,2-dimethyl-cis-decahydro-5-quinolinol with a syn orientation of the hydroxy and amino groups and different orientations of the methyl group relative to the methylene group at C(8)H2 were subjected to conformational analysis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::71a9d8cd3836125a34cf6a3e24c8fa59
https://doi.org/10.1007/bf00479371
https://doi.org/10.1007/bf00479371
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 37:922-926
The main product of the benzoylation of the hydrochloride of t-2-methyl-t-5-hydroxy-r-9-H-cis-decahydroquinoline, which exists in the conformation with the intramolecular H-bond, is the amidoester which can form a stable 1∶1 complex with benzoic ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::06a3940ba355a832e91ff101db2e3894
https://doi.org/10.1007/bf00957061
https://doi.org/10.1007/bf00957061