Zobrazeno 1 - 10
of 15
pro vyhledávání: '"V. I. Mukhanov"'
Autor:
M. M. Kaganskii, M. N. Preobrazhenskaya, S. G. Antonyan, G. V. Tananova, A. A. Sorokin, A. S. Kinzirskii, L. L. Mikhailevskaya, V. I. Mukhanov
Publikováno v:
Pharmaceutical Chemistry Journal. 28:446-451
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b145cd6bbc321a9e6e61f4ce341bff3a
https://doi.org/10.1007/bf02219244
https://doi.org/10.1007/bf02219244
Publikováno v:
Pharmaceutical Chemistry Journal. 13:603-611
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ca878f8e546893781a78c681665cb72
https://doi.org/10.1007/bf00778890
https://doi.org/10.1007/bf00778890
Autor:
M. N. Preobrazhenskaya, G. V. Chizhikov, T. P. Ivanova, V. I. Mukhanov, T. D. Miniker, G. I. Vornovitskaya
Publikováno v:
Pharmaceutical Chemistry Journal. 12:1118-1123
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76b8b2d0f7ba97f5f47d4051a1c93050
https://doi.org/10.1007/bf00777776
https://doi.org/10.1007/bf00777776
Autor:
T. N. Sokolova, V. I. Mukhanov, K. G. Zhirnova, M. N. Preobrazhenskaya, Ya. V. Dobrynin, T. G. Nikolaeva
Publikováno v:
Pharmaceutical Chemistry Journal. 16:211-216
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77e3eed9b9d56d5c42f35f9d95a5a1e9
https://doi.org/10.1007/bf00777273
https://doi.org/10.1007/bf00777273
Autor:
M. N. Preobrazhenskaya, Ya. V. Dobrynin, T. G. Nikolaeva, T. N. Sokolova, V. I. Mukhanov, K. G. Zhirnova
Publikováno v:
Pharmaceutical Chemistry Journal. 13:1034-1037
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::050a3cf60fbb1e3e0b000901a08252f1
https://doi.org/10.1007/bf00772248
https://doi.org/10.1007/bf00772248
Autor:
I. V. Yartseva, M. N. Preobrazhenskaya, V. I. Mukhanov, L. V. Ektova, T. D. Miniker, N. D. Chkanikov
Publikováno v:
Chemistry of Heterocyclic Compounds. 15:188-193
Condensation of 5- or 6-nitroindoline with L-arabinose gave 1-α-L-arabinopyranosyl-5 (or 6)-nitroindolines, which, after acetylation, dehydrogenation, and removal of the protective groups, are converted to 1-α-L-arabinopyranosyl-5(or 6)-nitroindole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::106edd4a31f29f6ca31855373e76a8fa
https://doi.org/10.1007/bf00480365
https://doi.org/10.1007/bf00480365
Autor:
M. N. Preobrazhenkaya, T. G. Nikolaeva, Ya. V. Dobrynin, V. I. Mukhanov, K. G. Zhirnova, T. N. Sokolova
Publikováno v:
Chemischer Informationsdienst. 13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::138d00816cf4611478de6cef99c13d72
https://doi.org/10.1002/chin.198239358
https://doi.org/10.1002/chin.198239358
Autor:
Maria N. Preobrazhenskaya, T. G. Nikolaeva, V. I. Mukhanov, K. G. Zhirnova, Ya. V. Dobrynin, T. N. Sokolova
Publikováno v:
Chemischer Informationsdienst. 11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c8d834d956060d3341a4188a4778149
https://doi.org/10.1002/chin.198011359
https://doi.org/10.1002/chin.198011359
Publikováno v:
Chemischer Informationsdienst. 10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa6a58916ad4c75d3916ada8b01a2fae
https://doi.org/10.1002/chin.197907332
https://doi.org/10.1002/chin.197907332
Autor:
M. N. Preobrazhenskaya, T. D. Miniker, I. V. Yartseva, V. I. Mukhanov, L. V. Ektova, N. D. Chkanikov
Publikováno v:
Chemischer Informationsdienst. 10
Condensation of 5- or 6-nitroindoline with L-arabinose gave 1-α-L-arabinopyranosyl-5 (or 6)-nitroindolines, which, after acetylation, dehydrogenation, and removal of the protective groups, are converted to 1-α-L-arabinopyranosyl-5(or 6)-nitroindole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c350b963f09a49800cd708d1499515a
https://doi.org/10.1002/chin.197925338
https://doi.org/10.1002/chin.197925338