Zobrazeno 1 - 10
of 13
pro vyhledávání: '"N. I. Mikerova"'
Autor:
N. I. Mikerova, V. G. Granik, Lyudmila M. Alekseeva, G. A. Bogdanova, V. V. Asnina, R. B. Parimbetova, V. A. Parshin, T. V. Golovko
Publikováno v:
Pharmaceutical Chemistry Journal. 28:236-242
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86e2c6285b4fe953ec64819fe5cc68b5
https://doi.org/10.1007/bf02219794
https://doi.org/10.1007/bf02219794
Autor:
N. I. Mikerova, E. K. Panisheva
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef9493134ea2330af1e5c8f6da6fa140
https://doi.org/10.1002/chin.199216197
https://doi.org/10.1002/chin.199216197
Autor:
E. K. Panisheva, V. M. Lyubchanskaya, L. S. Sarkisova, V. G. Granik, Yu. N. Sheinker, Lyudmila M. Alekseeva, N. I. Mikerova
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a6f4f605379d6ba65b48307decb2f9f
https://doi.org/10.1002/chin.199238146
https://doi.org/10.1002/chin.199238146
Autor:
N. I. Mikerova, V. G. Granik, T. V. Golovko, R. B. Parimbetova, V. V. Asnina, Lyudmila M. Alekseeva, G. A. Bogdanova, V. A. Parshin
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f84bec2dfd8ebe81e68a19e96529b0ec
https://doi.org/10.1002/chin.199437105
https://doi.org/10.1002/chin.199437105
Autor:
N. I. Mikerova, I. T. Fedyakina, A. A. Cherkasova, A. N. Fomina, I. S. Nikolaeva, G. Ya. Tikhomirova, N. I. Fadeeva, V. G. Granik, E. K. Panisheva
Publikováno v:
Pharmaceutical Chemistry Journal. 25:394-399
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0fdd41e37e1d18707b83ca120b45cce
https://doi.org/10.1007/bf00772140
https://doi.org/10.1007/bf00772140
Autor:
L. S. Sarkisova, V. G. Granik, Yu. N. Sheinker, Lyudmila M. Alekseeva, E. K. Panisheva, V. M. Lyubchanskaya, N. I. Mikerova
Publikováno v:
Chemistry of Heterocyclic Compounds. 27:369-375
A method has been developed for the selective N-alkylation of derivatives of 4-amino-5-hydroxy- and 6-amino-5-hydroxyindoles, based on the preliminary closure of the oxazolone ring by reaction with sodium cyanate and alkylation of the resulting oxazo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e335e8be35a012c316b47d62d3ff9df5
https://doi.org/10.1007/bf00480832
https://doi.org/10.1007/bf00480832
Publikováno v:
Chemistry of Heterocyclic Compounds. 26:274-278
The reaction of 2-chloro-5-methylbenzoquinone with Β-aminocrotonic ester derivatives was studied by PMR spectroscopy in CD3COOD. The spectra indicate the formation of intermediate hydroquinone and quinone derivatives, which subsequently transform in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b94ae9b26b198c66c6c8e95b83f8969a
https://doi.org/10.1007/bf00472542
https://doi.org/10.1007/bf00472542
Publikováno v:
Pharmaceutical Chemistry Journal. 25:391-393
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0293cdb5a67f41808d0a91176bd9ca54
https://doi.org/10.1007/bf00772139
https://doi.org/10.1007/bf00772139
Autor:
N. I. Mikerova, E. K. Panisheva, A. A. Cherkasova, L. V. Ershov, T. V. Pushkina, A. N. Fomina, I. S. Nikolaeva, V. G. Granik
Publikováno v:
Pharmaceutical Chemistry Journal. 25:238-240
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f200f9501bb54a72b1b9ce68cec05a9
https://doi.org/10.1007/bf00772102
https://doi.org/10.1007/bf00772102
Publikováno v:
ChemInform. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f841346f12b83beb2add98696206492
https://doi.org/10.1002/chin.199050162
https://doi.org/10.1002/chin.199050162