Zobrazeno 1 - 10
of 26
pro vyhledávání: '"M. V. Noritsina"'
Publikováno v:
Pharmaceutical Chemistry Journal. 35:424-428
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::58bd0b8faa4a6dccc235b65bbf3d3718
https://doi.org/10.1023/a:1013780122024
https://doi.org/10.1023/a:1013780122024
Publikováno v:
Pharmaceutical Chemistry Journal. 33:638-641
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c948b0636529b2e026fc0c471ea1e454
https://doi.org/10.1007/bf02974938
https://doi.org/10.1007/bf02974938
Publikováno v:
ChemInform. 31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b70c381d71053c334f7afbce02cc4d2f
https://doi.org/10.1002/chin.200016145
https://doi.org/10.1002/chin.200016145
Publikováno v:
ChemInform. 32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ad47febea47901c684ede921f65dfcb
https://doi.org/10.1002/chin.200151148
https://doi.org/10.1002/chin.200151148
Publikováno v:
Chemistry of Heterocyclic Compounds. 26:149-154
The formation of hydroxyalkylpyrrolidines from furan amines has been modeled using deuterium exchange. The stages of the reaction were established by comparing the 13C NMR spectra of the nondeuterated and deuterated pyrrolidinylalkanols, and the simi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33735c488872e322c3c8518b2a1c3e17
https://doi.org/10.1007/bf00499407
https://doi.org/10.1007/bf00499407
Publikováno v:
Pharmaceutical Chemistry Journal. 11:1219-1222
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1af276bf4490bf4b1473bc379986da8
https://doi.org/10.1007/bf00777740
https://doi.org/10.1007/bf00777740
Publikováno v:
Pharmaceutical Chemistry Journal. 21:435-438
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::101e3b97d96fc3f7d39dffeb21739ff4
https://doi.org/10.1007/bf00758635
https://doi.org/10.1007/bf00758635
Autor:
I. N. Klochkova, V. G. Andrianov, G. K. Kravtsova, Yu. T. Strukhkov, S. A. Lazarev, M. V. Noritsina
Publikováno v:
Chemistry of Heterocyclic Compounds. 19:180-183
Optically active 3-(5-methyl-2-pyrrolidinyl)-1-propanols and their tartrates were synthesized. The stereochemical structures of the latter were established by x-ray diffraction analysis and PMR and IR spectroscopy. The absolute configuration was dete
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c5974900e02634722ae756339b8a054
https://doi.org/10.1007/bf00506431
https://doi.org/10.1007/bf00506431
Publikováno v:
Chemistry of Heterocyclic Compounds. 20:1357-1360
Methods have been developed for the synthesis of cis- and trans-3-(5-alkyl-2-pyrrolidyl)alkanols. The catalyst isomerization of the stereoisomers has been studied, and configurational assignments of the isomers made on the basis of x-ray structural e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5fe8446384f3bd77e3184e6fcbcc6dd
https://doi.org/10.1007/bf00505959
https://doi.org/10.1007/bf00505959
Publikováno v:
Chemistry of Heterocyclic Compounds. 12:163-167
Phenyl-substituted pyrrolidylalkanols were synthesized by hydrogenation of the corresponding furan amines in acidic aqueous solution in the presence of nickel on diatomaceous earth. Terephthalates, carbamates, and other pyrrolidylalkanol derivatives
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54edda0bd359b60e1ba7880c9f32d5a8
https://doi.org/10.1007/bf00523960
https://doi.org/10.1007/bf00523960