Zobrazeno 1 - 3
of 3
pro vyhledávání: '"D. A. Shemyakina"'
Autor:
D. V. Eroshenko, D. A. Shemyakina, A. R. Galeev, I. G. Mokrushin, Maksim V. Dmitriev, L. V. Pavlogradskaya, Vladimir A. Glushkov, N. K. Zhukova
Publikováno v:
Russian Journal of Organic Chemistry. 55:1690-1697
The reaction of 30-bromo-3β,28-diacylbetulin with sodium azide afforded 30-azido-3β,28-diacyloxylup-20(29)-enes. The products were subjected to a CuI/TMEDA-catalyzed click reaction with ethynylferrocene to obtain the corresponding ferrocene-betulin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::768baf47a89691182c05542031f22146
https://doi.org/10.1134/s1070428019110083
https://doi.org/10.1134/s1070428019110083
Autor:
Vladimir A. Glushkov, I. A. Borisova, D. V. Eroshenko, L. V. Pavlogradskaya, D. A. Shemyakina
Publikováno v:
Russian Journal of Organic Chemistry. 54:126-130
Ferrocene conjugates with a lupane triterpenoid linked through a triazole ring and C3 or C6 hydrocarbon tether were synthesized by reaction of ferrocenylalkylazides with betulonic acid propargyl ester. Analogous conjugates were obtained from dehydroa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f3bbb9cf52bf5f20e574ad2376ff9e8
https://doi.org/10.1134/s1070428018010128
https://doi.org/10.1134/s1070428018010128
Publikováno v:
Russian Journal of Organic Chemistry. 50:1180-1183
Reactions of propargyl dehydroabietate with ferrocenylalkyl azides led to the formation of substituted 1,2,3-triazoles. The corresponding 1,2,3-triazoles formed in the reaction of ferrocenylalkyl azides with propargyl betulonic ester.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::196ab65d4a03753f2fbb6303a3e0cf0e
https://doi.org/10.1134/s1070428014080181
https://doi.org/10.1134/s1070428014080181