TY  - JOUR
AU  - Milić, Dragana
AU  - Šolaja, Bogdan A.
AU  - Došen-Mićović, Ljiljana
AU  - Ribár, B.
AU  - Kapor, A.
AU  - Sladić, Dušan
AU  - Gašić, M.J.
PY  - 1997
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/47
AB  - The preparation of substituted steroidal A-ring 1,4-quinones by nucleophilic addition results in pronounced regioselectivity at C(2), as confirmed by the X-ray analysis of 2-methoxy-2,5(10)-diene-1,4,17-trione. Conformational analysis (PM3, AM1, MNDO) of the suggested protonated intermediates and the difference in the relative energies of the transition states are considered. The results of cytotoxicity tests of selected quinones are also presented.
T2  - Journal of the Serbian Chemical Society
T1  - Structure and reactivity of steroidal quinones
VL  - 62
IS  - 9
SP  - 755
EP  - 768
UR  - https://hdl.handle.net/21.15107/rcub_cherry_47
ER  - 

@article{
author = "Milić, Dragana and Šolaja, Bogdan A. and Došen-Mićović, Ljiljana and Ribár, B. and Kapor, A. and Sladić, Dušan and Gašić, M.J.",
year = "1997",
abstract = "The preparation of substituted steroidal A-ring 1,4-quinones by nucleophilic addition results in pronounced regioselectivity at C(2), as confirmed by the X-ray analysis of 2-methoxy-2,5(10)-diene-1,4,17-trione. Conformational analysis (PM3, AM1, MNDO) of the suggested protonated intermediates and the difference in the relative energies of the transition states are considered. The results of cytotoxicity tests of selected quinones are also presented.",
journal = "Journal of the Serbian Chemical Society",
title = "Structure and reactivity of steroidal quinones",
volume = "62",
number = "9",
pages = "755-768",
url = "https://hdl.handle.net/21.15107/rcub_cherry_47"
}

Milić, D., Šolaja, B. A., Došen-Mićović, L., Ribár, B., Kapor, A., Sladić, D.,& Gašić, M.J.. (1997). Structure and reactivity of steroidal quinones. in Journal of the Serbian Chemical Society, 62(9), 755-768.
https://hdl.handle.net/21.15107/rcub_cherry_47

Milić D, Šolaja BA, Došen-Mićović L, Ribár B, Kapor A, Sladić D, Gašić M. Structure and reactivity of steroidal quinones. in Journal of the Serbian Chemical Society. 1997;62(9):755-768.
https://hdl.handle.net/21.15107/rcub_cherry_47 .

Milić, Dragana, Šolaja, Bogdan A., Došen-Mićović, Ljiljana, Ribár, B., Kapor, A., Sladić, Dušan, Gašić, M.J., "Structure and reactivity of steroidal quinones" in Journal of the Serbian Chemical Society, 62, no. 9 (1997):755-768,
https://hdl.handle.net/21.15107/rcub_cherry_47 .

TY  - JOUR
AU  - Gašić, M.J.
AU  - Zlatović, Mario
AU  - Ignjatović, Ljubiša
AU  - Putniković, B.
AU  - Sladić, Dušan
PY  - 1996
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/73
AB  - Electrochemical epoxidation of cholesterol and avarol dimethyl ether with bromide as heteromediator was performed, and its mechanism discussed. The influence of the solvent, the mediator concentration, and different electrolytic techniques on yield of the products was examined. Under optimal conditions, the yield of the cholesterol epoxides (5α,6α and 5β, 6β) was 88%, and of the corresponding epoxides of the avarol dimethyl ether 72%.
T2  - Journal of the Serbian Chemical Society
T1  - Improved electrochemical epoxidation of cholesterol and avarol dimethyl ether
VL  - 61
IS  - 11
SP  - 1033
EP  - 1037
UR  - https://hdl.handle.net/21.15107/rcub_cherry_73
ER  - 

@article{
author = "Gašić, M.J. and Zlatović, Mario and Ignjatović, Ljubiša and Putniković, B. and Sladić, Dušan",
year = "1996",
abstract = "Electrochemical epoxidation of cholesterol and avarol dimethyl ether with bromide as heteromediator was performed, and its mechanism discussed. The influence of the solvent, the mediator concentration, and different electrolytic techniques on yield of the products was examined. Under optimal conditions, the yield of the cholesterol epoxides (5α,6α and 5β, 6β) was 88%, and of the corresponding epoxides of the avarol dimethyl ether 72%.",
journal = "Journal of the Serbian Chemical Society",
title = "Improved electrochemical epoxidation of cholesterol and avarol dimethyl ether",
volume = "61",
number = "11",
pages = "1033-1037",
url = "https://hdl.handle.net/21.15107/rcub_cherry_73"
}

Gašić, M.J., Zlatović, M., Ignjatović, L., Putniković, B.,& Sladić, D.. (1996). Improved electrochemical epoxidation of cholesterol and avarol dimethyl ether. in Journal of the Serbian Chemical Society, 61(11), 1033-1037.
https://hdl.handle.net/21.15107/rcub_cherry_73

Gašić M, Zlatović M, Ignjatović L, Putniković B, Sladić D. Improved electrochemical epoxidation of cholesterol and avarol dimethyl ether. in Journal of the Serbian Chemical Society. 1996;61(11):1033-1037.
https://hdl.handle.net/21.15107/rcub_cherry_73 .

Gašić, M.J., Zlatović, Mario, Ignjatović, Ljubiša, Putniković, B., Sladić, Dušan, "Improved electrochemical epoxidation of cholesterol and avarol dimethyl ether" in Journal of the Serbian Chemical Society, 61, no. 11 (1996):1033-1037,
https://hdl.handle.net/21.15107/rcub_cherry_73 .

TY  - JOUR
AU  - Dogović, N.
AU  - Sladić, Dušan
AU  - Kljajić, Z.
AU  - Poznanović, S.
AU  - Gašić, M.J.
PY  - 1996
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/43
AB  - A lectin was isolated from the marine sponge Crambe crambe. The lectin is a monomeric glycoprotein with relative molecular mass of 14000. It agglutinates sheep and human red blood cells. The agglutination was found to be inhibited weakly only by L-fucose. The lectin has mitogenic properties, stimulating T-lymphocytes.
T2  - Journal of the Serbian Chemical Society
T1  - Isolation and partial characterization of a lectin from the marine sponge Crambe crambe
VL  - 61
IS  - 2
SP  - 83
EP  - 88
UR  - https://hdl.handle.net/21.15107/rcub_cherry_43
ER  - 

@article{
author = "Dogović, N. and Sladić, Dušan and Kljajić, Z. and Poznanović, S. and Gašić, M.J.",
year = "1996",
abstract = "A lectin was isolated from the marine sponge Crambe crambe. The lectin is a monomeric glycoprotein with relative molecular mass of 14000. It agglutinates sheep and human red blood cells. The agglutination was found to be inhibited weakly only by L-fucose. The lectin has mitogenic properties, stimulating T-lymphocytes.",
journal = "Journal of the Serbian Chemical Society",
title = "Isolation and partial characterization of a lectin from the marine sponge Crambe crambe",
volume = "61",
number = "2",
pages = "83-88",
url = "https://hdl.handle.net/21.15107/rcub_cherry_43"
}

Dogović, N., Sladić, D., Kljajić, Z., Poznanović, S.,& Gašić, M.J.. (1996). Isolation and partial characterization of a lectin from the marine sponge Crambe crambe. in Journal of the Serbian Chemical Society, 61(2), 83-88.
https://hdl.handle.net/21.15107/rcub_cherry_43

Dogović N, Sladić D, Kljajić Z, Poznanović S, Gašić M. Isolation and partial characterization of a lectin from the marine sponge Crambe crambe. in Journal of the Serbian Chemical Society. 1996;61(2):83-88.
https://hdl.handle.net/21.15107/rcub_cherry_43 .

Dogović, N., Sladić, Dušan, Kljajić, Z., Poznanović, S., Gašić, M.J., "Isolation and partial characterization of a lectin from the marine sponge Crambe crambe" in Journal of the Serbian Chemical Society, 61, no. 2 (1996):83-88,
https://hdl.handle.net/21.15107/rcub_cherry_43 .

TY  - JOUR
AU  - Cozzolino, R.
AU  - De Giulio, A.
AU  - De Rosa, S.
AU  - Strazzuixllo, G.
AU  - Gašić, M.J.
AU  - Sladić, Dušan
AU  - Zlatović, Mario
PY  - 1990
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/17
AB  - Nine amino derivatives, compounds 3-11. of avarone were synthesized. Their antibacterial and cytotoxic activities are evaluated, and the results of a prescreen for antitumor effects are reported.
PB  - American Chemical Society
T2  - Journal of Natural Products
T1  - Biological activities of avarol derivatives, 1. Amino derivatives
VL  - 53
IS  - 3
SP  - 699
EP  - 702
DO  - 10.1021/np50069a027
ER  - 

@article{
author = "Cozzolino, R. and De Giulio, A. and De Rosa, S. and Strazzuixllo, G. and Gašić, M.J. and Sladić, Dušan and Zlatović, Mario",
year = "1990",
abstract = "Nine amino derivatives, compounds 3-11. of avarone were synthesized. Their antibacterial and cytotoxic activities are evaluated, and the results of a prescreen for antitumor effects are reported.",
publisher = "American Chemical Society",
journal = "Journal of Natural Products",
title = "Biological activities of avarol derivatives, 1. Amino derivatives",
volume = "53",
number = "3",
pages = "699-702",
doi = "10.1021/np50069a027"
}

Cozzolino, R., De Giulio, A., De Rosa, S., Strazzuixllo, G., Gašić, M.J., Sladić, D.,& Zlatović, M.. (1990). Biological activities of avarol derivatives, 1. Amino derivatives. in Journal of Natural Products
American Chemical Society., 53(3), 699-702.
https://doi.org/10.1021/np50069a027

Cozzolino R, De Giulio A, De Rosa S, Strazzuixllo G, Gašić M, Sladić D, Zlatović M. Biological activities of avarol derivatives, 1. Amino derivatives. in Journal of Natural Products. 1990;53(3):699-702.
doi:10.1021/np50069a027 .

Cozzolino, R., De Giulio, A., De Rosa, S., Strazzuixllo, G., Gašić, M.J., Sladić, Dušan, Zlatović, Mario, "Biological activities of avarol derivatives, 1. Amino derivatives" in Journal of Natural Products, 53, no. 3 (1990):699-702,
https://doi.org/10.1021/np50069a027 . .

TY  - JOUR
AU  - Tabaković, I.
AU  - Davidović, A.
AU  - Müller, W.E.G.
AU  - Zahn, R.K.
AU  - Sladić, Dušan
AU  - Dogović, N.
AU  - Gašić, M.J.
PY  - 1987
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/71
AB  - The redox reactivity of avarone and avarol, a quinone/hydroquinone couple isolated from the marine sponge Dysidea avara, was investigated by cyclic voltammetry, using a glassy carbon electrode. Both oxidation of avarol and reduction of avarone in aqueous ethanol (1:1 V/V) take place by a 2 e- process at a wide range of pH values; in acetonitrile, however, the reduction of avarone occurs as a stepwise electron transfer process. The mechanisms, as well as the scope and limitations of the method are discussed with reference to the biological activity of the two sesquiterpenoids. © 1987.
T2  - Bioelectrochemistry and Bioenergetics
T1  - Electrochemical reactivity of biologically active quinone/hydroquinone sesquiterpenoids on glassy carbon electrodes
VL  - 17
IS  - 3
SP  - 567
EP  - 577
DO  - 10.1016/0302-4598(87)80064-8
ER  - 

@article{
author = "Tabaković, I. and Davidović, A. and Müller, W.E.G. and Zahn, R.K. and Sladić, Dušan and Dogović, N. and Gašić, M.J.",
year = "1987",
abstract = "The redox reactivity of avarone and avarol, a quinone/hydroquinone couple isolated from the marine sponge Dysidea avara, was investigated by cyclic voltammetry, using a glassy carbon electrode. Both oxidation of avarol and reduction of avarone in aqueous ethanol (1:1 V/V) take place by a 2 e- process at a wide range of pH values; in acetonitrile, however, the reduction of avarone occurs as a stepwise electron transfer process. The mechanisms, as well as the scope and limitations of the method are discussed with reference to the biological activity of the two sesquiterpenoids. © 1987.",
journal = "Bioelectrochemistry and Bioenergetics",
title = "Electrochemical reactivity of biologically active quinone/hydroquinone sesquiterpenoids on glassy carbon electrodes",
volume = "17",
number = "3",
pages = "567-577",
doi = "10.1016/0302-4598(87)80064-8"
}

Tabaković, I., Davidović, A., Müller, W.E.G., Zahn, R.K., Sladić, D., Dogović, N.,& Gašić, M.J.. (1987). Electrochemical reactivity of biologically active quinone/hydroquinone sesquiterpenoids on glassy carbon electrodes. in Bioelectrochemistry and Bioenergetics, 17(3), 567-577.
https://doi.org/10.1016/0302-4598(87)80064-8

Tabaković I, Davidović A, Müller W, Zahn R, Sladić D, Dogović N, Gašić M. Electrochemical reactivity of biologically active quinone/hydroquinone sesquiterpenoids on glassy carbon electrodes. in Bioelectrochemistry and Bioenergetics. 1987;17(3):567-577.
doi:10.1016/0302-4598(87)80064-8 .

Tabaković, I., Davidović, A., Müller, W.E.G., Zahn, R.K., Sladić, Dušan, Dogović, N., Gašić, M.J., "Electrochemical reactivity of biologically active quinone/hydroquinone sesquiterpenoids on glassy carbon electrodes" in Bioelectrochemistry and Bioenergetics, 17, no. 3 (1987):567-577,
https://doi.org/10.1016/0302-4598(87)80064-8 . .