Pavlović, Radoslav Z.

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9016d361-7f32-4328-85fd-87e8067efada
  • Pavlović, Radoslav Z. (3)
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Author's Bibliography

Cycloaddition Reactions of Azomethine Ylides and 1,3-Dienes on the C-2v-Symmetrical Pentakisadduct of C-60

Pavlović, Radoslav Z.; Mitrović, Aleksandra D.; Coldren, William H.; Bjelaković, Mira S.; Hadad, Christopher M.; Maslak, Veselin; Milić, Dragana

(Amer Chemical Soc, Washington, 2018) 

TY  - JOUR
AU  - Pavlović, Radoslav Z.
AU  - Mitrović, Aleksandra D.
AU  - Coldren, William H.
AU  - Bjelaković, Mira S.
AU  - Hadad, Christopher M.
AU  - Maslak, Veselin
AU  - Milić, Dragana
PY  - 2018
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2105
AB  - The reactivity of the C-2v-symmetric pentakisadduct of C-60 with azomethine ylides and conjugated dienes was studied experimentally and computationally. This derivative possesses four [6,6] double bonds, each with unique electrophilicity. The Diels-Alder reaction studied is a regiospecific, kinetically and thermodynamically guided [4 + 2] process producing [5:1]-hexaadducts with an octahedral addition pattern. The kinetically controlled Prato reaction gives a mixture of regioisomeric [5:1]-hexaadducts. The synthesis of geometrically well-defined supramolecular architectures may benefit from these new types of highly functionalized [5:1]-hexaadducts.
PB  - Amer Chemical Soc, Washington
T2  - Journal of Organic Chemistry
T1  - Cycloaddition Reactions of Azomethine Ylides and 1,3-Dienes on the C-2v-Symmetrical Pentakisadduct of C-60
VL  - 83
IS  - 4
SP  - 2166
EP  - 2172
DO  - 10.1021/acs.joc.7b03083
ER  - 
@article{
author = "Pavlović, Radoslav Z. and Mitrović, Aleksandra D. and Coldren, William H. and Bjelaković, Mira S. and Hadad, Christopher M. and Maslak, Veselin and Milić, Dragana",
year = "2018",
abstract = "The reactivity of the C-2v-symmetric pentakisadduct of C-60 with azomethine ylides and conjugated dienes was studied experimentally and computationally. This derivative possesses four [6,6] double bonds, each with unique electrophilicity. The Diels-Alder reaction studied is a regiospecific, kinetically and thermodynamically guided [4 + 2] process producing [5:1]-hexaadducts with an octahedral addition pattern. The kinetically controlled Prato reaction gives a mixture of regioisomeric [5:1]-hexaadducts. The synthesis of geometrically well-defined supramolecular architectures may benefit from these new types of highly functionalized [5:1]-hexaadducts.",
publisher = "Amer Chemical Soc, Washington",
journal = "Journal of Organic Chemistry",
title = "Cycloaddition Reactions of Azomethine Ylides and 1,3-Dienes on the C-2v-Symmetrical Pentakisadduct of C-60",
volume = "83",
number = "4",
pages = "2166-2172",
doi = "10.1021/acs.joc.7b03083"
}
Pavlović, R. Z., Mitrović, A. D., Coldren, W. H., Bjelaković, M. S., Hadad, C. M., Maslak, V.,& Milić, D.. (2018). Cycloaddition Reactions of Azomethine Ylides and 1,3-Dienes on the C-2v-Symmetrical Pentakisadduct of C-60. in Journal of Organic Chemistry
Amer Chemical Soc, Washington., 83(4), 2166-2172.
https://doi.org/10.1021/acs.joc.7b03083
Pavlović RZ, Mitrović AD, Coldren WH, Bjelaković MS, Hadad CM, Maslak V, Milić D. Cycloaddition Reactions of Azomethine Ylides and 1,3-Dienes on the C-2v-Symmetrical Pentakisadduct of C-60. in Journal of Organic Chemistry. 2018;83(4):2166-2172.
doi:10.1021/acs.joc.7b03083 .
Pavlović, Radoslav Z., Mitrović, Aleksandra D., Coldren, William H., Bjelaković, Mira S., Hadad, Christopher M., Maslak, Veselin, Milić, Dragana, "Cycloaddition Reactions of Azomethine Ylides and 1,3-Dienes on the C-2v-Symmetrical Pentakisadduct of C-60" in Journal of Organic Chemistry, 83, no. 4 (2018):2166-2172,
https://doi.org/10.1021/acs.joc.7b03083 . .
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Diamide-based fullerosteroidal and disteroidal [2] rotaxanes: solvent-induced macrocycle translocation and/or unthreading

Pavlović, Radoslav Z.; Bjelaković, Mira S.; Milić, Dragana

(Royal Soc Chemistry, Cambridge, 2016) 

TY  - JOUR
AU  - Pavlović, Radoslav Z.
AU  - Bjelaković, Mira S.
AU  - Milić, Dragana
PY  - 2016
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1921
AB  - The synthesis, characterization and behaviour of two novel Leigh-type amide [2]rotaxanes are reported. NMR study shows that fullerosteroidal and disteroidal rotaxanes occur in a peptide co-conformation in CDCl3. [D-6]DMSO induces fast unthreading of disteroidal rotaxane, which includes steroid co-conformers as intermediates. On the other hand, fullerosteroidal rotaxane undergoes predominantly a shuttling process occupying the stacked co-conformation, whereas unthreading is very slow in comparison with its disteroidal analogue (25% after 7 days). Moreover, organogelation and self-organization properties were studied. It was found that disteroidal rotaxane is an organogelator and its SEM image shows that it forms a branched film-like network in a PhMe/EtOAc 1 : 1 mixture.
PB  - Royal Soc Chemistry, Cambridge
T2  - RSC Advances
T1  - Diamide-based fullerosteroidal and disteroidal [2] rotaxanes: solvent-induced macrocycle translocation and/or unthreading
VL  - 6
IS  - 43
SP  - 37246
EP  - 37253
DO  - 10.1039/c6ra03872g
ER  - 
@article{
author = "Pavlović, Radoslav Z. and Bjelaković, Mira S. and Milić, Dragana",
year = "2016",
abstract = "The synthesis, characterization and behaviour of two novel Leigh-type amide [2]rotaxanes are reported. NMR study shows that fullerosteroidal and disteroidal rotaxanes occur in a peptide co-conformation in CDCl3. [D-6]DMSO induces fast unthreading of disteroidal rotaxane, which includes steroid co-conformers as intermediates. On the other hand, fullerosteroidal rotaxane undergoes predominantly a shuttling process occupying the stacked co-conformation, whereas unthreading is very slow in comparison with its disteroidal analogue (25% after 7 days). Moreover, organogelation and self-organization properties were studied. It was found that disteroidal rotaxane is an organogelator and its SEM image shows that it forms a branched film-like network in a PhMe/EtOAc 1 : 1 mixture.",
publisher = "Royal Soc Chemistry, Cambridge",
journal = "RSC Advances",
title = "Diamide-based fullerosteroidal and disteroidal [2] rotaxanes: solvent-induced macrocycle translocation and/or unthreading",
volume = "6",
number = "43",
pages = "37246-37253",
doi = "10.1039/c6ra03872g"
}
Pavlović, R. Z., Bjelaković, M. S.,& Milić, D.. (2016). Diamide-based fullerosteroidal and disteroidal [2] rotaxanes: solvent-induced macrocycle translocation and/or unthreading. in RSC Advances
Royal Soc Chemistry, Cambridge., 6(43), 37246-37253.
https://doi.org/10.1039/c6ra03872g
Pavlović RZ, Bjelaković MS, Milić D. Diamide-based fullerosteroidal and disteroidal [2] rotaxanes: solvent-induced macrocycle translocation and/or unthreading. in RSC Advances. 2016;6(43):37246-37253.
doi:10.1039/c6ra03872g .
Pavlović, Radoslav Z., Bjelaković, Mira S., Milić, Dragana, "Diamide-based fullerosteroidal and disteroidal [2] rotaxanes: solvent-induced macrocycle translocation and/or unthreading" in RSC Advances, 6, no. 43 (2016):37246-37253,
https://doi.org/10.1039/c6ra03872g . .
1
1

Supplementary data for the article: Pavlović, R. Z.; Bjelaković, M. S.; Milić, D. Diamide-Based Fullerosteroidal and Disteroidal [2] Rotaxanes: Solvent-Induced Macrocycle Translocation and/or Unthreading. RSC Advances 2016, 6 (43), 37246–37253. https://doi.org/10.1039/c6ra03872g

Pavlović, Radoslav Z.; Bjelaković, Mira S.; Milić, Dragana

(Royal Soc Chemistry, Cambridge, 2016) 

TY  - DATA
AU  - Pavlović, Radoslav Z.
AU  - Bjelaković, Mira S.
AU  - Milić, Dragana
PY  - 2016
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3443
PB  - Royal Soc Chemistry, Cambridge
T2  - RSC Advances
T1  - Supplementary data for the article: Pavlović, R. Z.; Bjelaković, M. S.; Milić, D. Diamide-Based Fullerosteroidal and Disteroidal [2] Rotaxanes: Solvent-Induced Macrocycle Translocation and/or Unthreading. RSC Advances 2016, 6 (43), 37246–37253. https://doi.org/10.1039/c6ra03872g
UR  - https://hdl.handle.net/21.15107/rcub_cherry_3443
ER  - 
@misc{
author = "Pavlović, Radoslav Z. and Bjelaković, Mira S. and Milić, Dragana",
year = "2016",
publisher = "Royal Soc Chemistry, Cambridge",
journal = "RSC Advances",
title = "Supplementary data for the article: Pavlović, R. Z.; Bjelaković, M. S.; Milić, D. Diamide-Based Fullerosteroidal and Disteroidal [2] Rotaxanes: Solvent-Induced Macrocycle Translocation and/or Unthreading. RSC Advances 2016, 6 (43), 37246–37253. https://doi.org/10.1039/c6ra03872g",
url = "https://hdl.handle.net/21.15107/rcub_cherry_3443"
}
Pavlović, R. Z., Bjelaković, M. S.,& Milić, D.. (2016). Supplementary data for the article: Pavlović, R. Z.; Bjelaković, M. S.; Milić, D. Diamide-Based Fullerosteroidal and Disteroidal [2] Rotaxanes: Solvent-Induced Macrocycle Translocation and/or Unthreading. RSC Advances 2016, 6 (43), 37246–37253. https://doi.org/10.1039/c6ra03872g. in RSC Advances
Royal Soc Chemistry, Cambridge..
https://hdl.handle.net/21.15107/rcub_cherry_3443
Pavlović RZ, Bjelaković MS, Milić D. Supplementary data for the article: Pavlović, R. Z.; Bjelaković, M. S.; Milić, D. Diamide-Based Fullerosteroidal and Disteroidal [2] Rotaxanes: Solvent-Induced Macrocycle Translocation and/or Unthreading. RSC Advances 2016, 6 (43), 37246–37253. https://doi.org/10.1039/c6ra03872g. in RSC Advances. 2016;.
https://hdl.handle.net/21.15107/rcub_cherry_3443 .
Pavlović, Radoslav Z., Bjelaković, Mira S., Milić, Dragana, "Supplementary data for the article: Pavlović, R. Z.; Bjelaković, M. S.; Milić, D. Diamide-Based Fullerosteroidal and Disteroidal [2] Rotaxanes: Solvent-Induced Macrocycle Translocation and/or Unthreading. RSC Advances 2016, 6 (43), 37246–37253. https://doi.org/10.1039/c6ra03872g" in RSC Advances (2016),
https://hdl.handle.net/21.15107/rcub_cherry_3443 .