Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Bjelaković, Mira S."'
Autor:
Kop, Tatjana J., Bjelaković, Mira S., Živković, Ljiljana, Žekić, Andrijana, Milić, Dragana R.
Publikováno v:
In Colloids and Surfaces A: Physicochemical and Engineering Aspects 5 September 2022 648
Autor:
Jovanović Dragana, Stanojković Jovana, Halilović Dženeta, Kolašinac Rejhana, Kop Tatjana J., Bjelaković Mira S., Milić Dragana R.
Publikováno v:
Journal of the Serbian Chemical Society, Vol 86, Iss 11, Pp 1023-1037 (2021)
A large series of disubstituted fulleropyrrolidines was synthesized and analyzed by cyclic voltammetry. The three main groups of target compounds differ by a flexible N-chain, while their further diversity was achieved by the introduction of various
Externí odkaz:
https://doaj.org/article/b93fefd32123482c960b59686592e929
Autor:
Kop, Tatjana J., Jakovljević, Dragica M., Živković, Ljiljana S., Žekić, Andrijana, Beškoski, Vladimir P., Milić, Dragana R., Gojgić-Cvijović, Gordana D., Bjelaković, Mira S.
Publikováno v:
In European Polymer Journal 15 January 2020 123
Publikováno v:
In Tetrahedron 14 December 2017 73(50):7073-7078
Publikováno v:
In Tetrahedron 11 November 2014 70(45):8564-8570
Autor:
Bjelaković, Mira S., Krstić, Natalija M., Milić, Dragana R., Kop, Tatjana J., Robeyns, Koen, Pavlović, Vladimir D.
Publikováno v:
In Tetrahedron 9 September 2012 68(36):7479-7488
Autor:
Krstić Natalija M., Bjelaković Mira S., Dabović Milan M., Lorenc Ljubinka B., Pavlović Vladimir D.
Publikováno v:
Journal of the Serbian Chemical Society, Vol 69, Iss 6, Pp 413-420 (2004)
Beckmann rearrangement of (Z)-cholest-4-en-6-one oxime (4) (prepared in 4 steps starting from cholest-5-en-3β-ol ο1)) with thionyl chloride in dioxane solution afforded an enamide-type lactam, i.e. 7-aza-B-homocholest-4-en-6-one (6) as a single pro
Externí odkaz:
https://doaj.org/article/64fec7225b4e4c8ab3576b73746a221c
Publikováno v:
Journal of the Serbian Chemical Society, Vol 68, Iss 4-5, Pp 303-312 (2003)
The acid-catalyzed reaction of (Z)- and (E)-B-nor-5,10-seco-ketones 2 and 3 resulted in an intramolecular cyclization to give the 5-hydroxy-A-nor-1β,5β-10(19)-methylidene derivative 8, the 5β-hydroxy-A-nor-1(10)-unsaturated compound 9 and the 5β,
Externí odkaz:
https://doaj.org/article/19f5999ec26c4ac89da44da42acd7464
Publikováno v:
Journal of the Serbian Chemical Society, Vol 68, Iss 11, Pp 785-794 (2003)
5-hydroxy-1-oxo-5α-cholestan-3β-yl acetate (11) was prepared in 5 steps starting from (E)-3β-acetoxy-5,10-seco-1(10)-cholesten-5-one (6). Treatment of the 1-oxo-5-hydroxy derivative 11 with lead tetraacetate (LTA) (under thermal or hypoiodite cond
Externí odkaz:
https://doaj.org/article/341de0f4f47b4f2ab28d6e17802da8cd
Publikováno v:
Journal of the Serbian Chemical Society, Vol 67, Iss 2, Pp 69-75 (2002)
B-Norcholestane epoxide 2 is reduced with lithium aluminium hydride to give either the 3β,6α-diol 3 or the corresponding 3β,5α-diol 4, depending on the quality of the reducing reagent employed. Aplausible mechanistic explanation of the obtained r
Externí odkaz:
https://doaj.org/article/7b2166f05e79461880f3ae7af606a0ed