TY  - JOUR
AU  - Avramović, Ljiljana
AU  - Ivanović, Evica R.
AU  - Maksimović, Vesna
AU  - Pavlović, Miroslav M.
AU  - Vuković, Marina
AU  - Stevanović, Jasmina
AU  - Nikolić, Nebojša D.
PY  - 2018
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/5223
AB  - Silver dendritic nanonstructures obtained by the potentiostatic electrolysis from different electrolytes at different overpotentials were characterized by the scanning electron microscopy (SEM) technique and X-ray diffraction analysis of the produced particles. The needle-like and fern-like dendrites were formed from the nitrate electrolyte at overpotentials inside and outside plateaus of the limiting diffusion current density, respectively. The three-dimensional pine-like dendrites constructed from approximately spherical grains were formed from the ammonium electrolyte at overpotentials both inside and outside plateaus of the limiting diffusion current density. The morphology of silver dendrites was correlated with their crystal structure at the semi quantiative level. The change of crystal orientation from the strong (111) preferred orientation for the needle-like dendrites to almost randomly orientied spherical grains in the pine-like dendrites obtained at the overpotential outside the plateau of the limiting diffusion current density was observed. This trend in change of crystal orientation and morphology of Ag nanostructures was accompanied by considerable increase of the specific surface area (SSA) of the produced powders. The average crystallite sizes were in the range of 38-50 nm, proving nanostructural character of the formed Ag particles.
PB  - Elsevier
T2  - Transactions of Nonferrous Metals Society of China
T1  - Correlation between crystal structure and morphology of potentiostatically electrodeposited silver dendritic nanostructures
VL  - 28
IS  - 9
SP  - 1903
EP  - 1912
DO  - 10.1016/S1003-6326(18)64835-6
ER  - 

@article{
author = "Avramović, Ljiljana and Ivanović, Evica R. and Maksimović, Vesna and Pavlović, Miroslav M. and Vuković, Marina and Stevanović, Jasmina and Nikolić, Nebojša D.",
year = "2018",
abstract = "Silver dendritic nanonstructures obtained by the potentiostatic electrolysis from different electrolytes at different overpotentials were characterized by the scanning electron microscopy (SEM) technique and X-ray diffraction analysis of the produced particles. The needle-like and fern-like dendrites were formed from the nitrate electrolyte at overpotentials inside and outside plateaus of the limiting diffusion current density, respectively. The three-dimensional pine-like dendrites constructed from approximately spherical grains were formed from the ammonium electrolyte at overpotentials both inside and outside plateaus of the limiting diffusion current density. The morphology of silver dendrites was correlated with their crystal structure at the semi quantiative level. The change of crystal orientation from the strong (111) preferred orientation for the needle-like dendrites to almost randomly orientied spherical grains in the pine-like dendrites obtained at the overpotential outside the plateau of the limiting diffusion current density was observed. This trend in change of crystal orientation and morphology of Ag nanostructures was accompanied by considerable increase of the specific surface area (SSA) of the produced powders. The average crystallite sizes were in the range of 38-50 nm, proving nanostructural character of the formed Ag particles.",
publisher = "Elsevier",
journal = "Transactions of Nonferrous Metals Society of China",
title = "Correlation between crystal structure and morphology of potentiostatically electrodeposited silver dendritic nanostructures",
volume = "28",
number = "9",
pages = "1903-1912",
doi = "10.1016/S1003-6326(18)64835-6"
}

Avramović, L., Ivanović, E. R., Maksimović, V., Pavlović, M. M., Vuković, M., Stevanović, J.,& Nikolić, N. D.. (2018). Correlation between crystal structure and morphology of potentiostatically electrodeposited silver dendritic nanostructures. in Transactions of Nonferrous Metals Society of China
Elsevier., 28(9), 1903-1912.
https://doi.org/10.1016/S1003-6326(18)64835-6

Avramović L, Ivanović ER, Maksimović V, Pavlović MM, Vuković M, Stevanović J, Nikolić ND. Correlation between crystal structure and morphology of potentiostatically electrodeposited silver dendritic nanostructures. in Transactions of Nonferrous Metals Society of China. 2018;28(9):1903-1912.
doi:10.1016/S1003-6326(18)64835-6 .

Avramović, Ljiljana, Ivanović, Evica R., Maksimović, Vesna, Pavlović, Miroslav M., Vuković, Marina, Stevanović, Jasmina, Nikolić, Nebojša D., "Correlation between crystal structure and morphology of potentiostatically electrodeposited silver dendritic nanostructures" in Transactions of Nonferrous Metals Society of China, 28, no. 9 (2018):1903-1912,
https://doi.org/10.1016/S1003-6326(18)64835-6 . .

TY  - JOUR
AU  - Jevtić, Ivana I.
AU  - Došen-Mićović, Ljiljana
AU  - Ivanović, Evica R.
AU  - Todorović, Nina
AU  - Ivanović, Milovan
PY  - 2017
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2492
AB  - The synthesis of orthogonally protected cis- and trans-3-amino-4-anilidopiperidine derivatives has been accomplished in six steps, starting from readily accessible 4-piperidone derivatives. The last three steps, i.e., N-acylation, Hofmann rearrangement, and carbamate cleavage, involved separated (+/-)-cis and (+/-)-trans intermediates. Complete retention of configuration was observed at position 3 of the piperidine ring. Specifically protected positions 1 and 3 at the piperidine scaffold allow for selective deprotection and introduction of diverse substituents at the respective nitrogen sites. The orthogonally protected anilidopiperidines open avenues to potentially pharmacologically active compounds, including opioids and various bivalent ligands for G protein-coupled receptors. In addition, a prototype of a novel class of fentanyl derivatives, possessing a 3-amino group, was synthesized by using the same approach.
PB  - Georg Thieme Verlag Kg, Stuttgart
T2  - Synthesis, Stuttgart
T1  - Synthesis of Orthogonally Protected (+/-)-3-Amino-4-anilidopiperidines and (+/-)-3-N-Carbomethoxyfentanyl
VL  - 49
IS  - 14
SP  - 3126
EP  - 3136
DO  - 10.1055/s-0036-1588985
ER  - 

@article{
author = "Jevtić, Ivana I. and Došen-Mićović, Ljiljana and Ivanović, Evica R. and Todorović, Nina and Ivanović, Milovan",
year = "2017",
abstract = "The synthesis of orthogonally protected cis- and trans-3-amino-4-anilidopiperidine derivatives has been accomplished in six steps, starting from readily accessible 4-piperidone derivatives. The last three steps, i.e., N-acylation, Hofmann rearrangement, and carbamate cleavage, involved separated (+/-)-cis and (+/-)-trans intermediates. Complete retention of configuration was observed at position 3 of the piperidine ring. Specifically protected positions 1 and 3 at the piperidine scaffold allow for selective deprotection and introduction of diverse substituents at the respective nitrogen sites. The orthogonally protected anilidopiperidines open avenues to potentially pharmacologically active compounds, including opioids and various bivalent ligands for G protein-coupled receptors. In addition, a prototype of a novel class of fentanyl derivatives, possessing a 3-amino group, was synthesized by using the same approach.",
publisher = "Georg Thieme Verlag Kg, Stuttgart",
journal = "Synthesis, Stuttgart",
title = "Synthesis of Orthogonally Protected (+/-)-3-Amino-4-anilidopiperidines and (+/-)-3-N-Carbomethoxyfentanyl",
volume = "49",
number = "14",
pages = "3126-3136",
doi = "10.1055/s-0036-1588985"
}

Jevtić, I. I., Došen-Mićović, L., Ivanović, E. R., Todorović, N.,& Ivanović, M.. (2017). Synthesis of Orthogonally Protected (+/-)-3-Amino-4-anilidopiperidines and (+/-)-3-N-Carbomethoxyfentanyl. in Synthesis, Stuttgart
Georg Thieme Verlag Kg, Stuttgart., 49(14), 3126-3136.
https://doi.org/10.1055/s-0036-1588985

Jevtić II, Došen-Mićović L, Ivanović ER, Todorović N, Ivanović M. Synthesis of Orthogonally Protected (+/-)-3-Amino-4-anilidopiperidines and (+/-)-3-N-Carbomethoxyfentanyl. in Synthesis, Stuttgart. 2017;49(14):3126-3136.
doi:10.1055/s-0036-1588985 .

Jevtić, Ivana I., Došen-Mićović, Ljiljana, Ivanović, Evica R., Todorović, Nina, Ivanović, Milovan, "Synthesis of Orthogonally Protected (+/-)-3-Amino-4-anilidopiperidines and (+/-)-3-N-Carbomethoxyfentanyl" in Synthesis, Stuttgart, 49, no. 14 (2017):3126-3136,
https://doi.org/10.1055/s-0036-1588985 . .

TY  - JOUR
AU  - Jevtić, Ivana I.
AU  - Došen-Mićović, Ljiljana
AU  - Ivanović, Evica R.
AU  - Todorović, Nina
AU  - Ivanović, Milovan
PY  - 2017
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3248
AB  - The synthesis of orthogonally protected cis- and trans-3-amino-4-anilidopiperidine derivatives has been accomplished in six steps, starting from readily accessible 4-piperidone derivatives. The last three steps, i.e., N-acylation, Hofmann rearrangement, and carbamate cleavage, involved separated (+/-)-cis and (+/-)-trans intermediates. Complete retention of configuration was observed at position 3 of the piperidine ring. Specifically protected positions 1 and 3 at the piperidine scaffold allow for selective deprotection and introduction of diverse substituents at the respective nitrogen sites. The orthogonally protected anilidopiperidines open avenues to potentially pharmacologically active compounds, including opioids and various bivalent ligands for G protein-coupled receptors. In addition, a prototype of a novel class of fentanyl derivatives, possessing a 3-amino group, was synthesized by using the same approach.
PB  - Georg Thieme Verlag Kg, Stuttgart
T2  - Synthesis
T1  - Synthesis of Orthogonally Protected (±)-3-Amino-4-anilidopiperidines and (±)-3- N -Carbomethoxyfentanyl
VL  - 49
IS  - 14
SP  - 3126
EP  - 3136
DO  - 10.1055/s-0036-1588985
ER  - 

@article{
author = "Jevtić, Ivana I. and Došen-Mićović, Ljiljana and Ivanović, Evica R. and Todorović, Nina and Ivanović, Milovan",
year = "2017",
abstract = "The synthesis of orthogonally protected cis- and trans-3-amino-4-anilidopiperidine derivatives has been accomplished in six steps, starting from readily accessible 4-piperidone derivatives. The last three steps, i.e., N-acylation, Hofmann rearrangement, and carbamate cleavage, involved separated (+/-)-cis and (+/-)-trans intermediates. Complete retention of configuration was observed at position 3 of the piperidine ring. Specifically protected positions 1 and 3 at the piperidine scaffold allow for selective deprotection and introduction of diverse substituents at the respective nitrogen sites. The orthogonally protected anilidopiperidines open avenues to potentially pharmacologically active compounds, including opioids and various bivalent ligands for G protein-coupled receptors. In addition, a prototype of a novel class of fentanyl derivatives, possessing a 3-amino group, was synthesized by using the same approach.",
publisher = "Georg Thieme Verlag Kg, Stuttgart",
journal = "Synthesis",
title = "Synthesis of Orthogonally Protected (±)-3-Amino-4-anilidopiperidines and (±)-3- N -Carbomethoxyfentanyl",
volume = "49",
number = "14",
pages = "3126-3136",
doi = "10.1055/s-0036-1588985"
}

Jevtić, I. I., Došen-Mićović, L., Ivanović, E. R., Todorović, N.,& Ivanović, M.. (2017). Synthesis of Orthogonally Protected (±)-3-Amino-4-anilidopiperidines and (±)-3- N -Carbomethoxyfentanyl. in Synthesis
Georg Thieme Verlag Kg, Stuttgart., 49(14), 3126-3136.
https://doi.org/10.1055/s-0036-1588985

Jevtić II, Došen-Mićović L, Ivanović ER, Todorović N, Ivanović M. Synthesis of Orthogonally Protected (±)-3-Amino-4-anilidopiperidines and (±)-3- N -Carbomethoxyfentanyl. in Synthesis. 2017;49(14):3126-3136.
doi:10.1055/s-0036-1588985 .

Jevtić, Ivana I., Došen-Mićović, Ljiljana, Ivanović, Evica R., Todorović, Nina, Ivanović, Milovan, "Synthesis of Orthogonally Protected (±)-3-Amino-4-anilidopiperidines and (±)-3- N -Carbomethoxyfentanyl" in Synthesis, 49, no. 14 (2017):3126-3136,
https://doi.org/10.1055/s-0036-1588985 . .

TY  - DATA
AU  - Jevtić, Ivana I.
AU  - Došen-Mićović, Ljiljana
AU  - Ivanović, Evica R.
AU  - Todorović, Nina
AU  - Ivanović, Milovan
PY  - 2017
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3249
PB  - Georg Thieme Verlag Kg, Stuttgart
T2  - Synthesis
T1  - Supplementary material for the article: Jevtić, I. I.; Došen-Mićović, L. I.; Ivanović, E. R.; Todorović, N. M.; Ivanović, M. D. Synthesis of Orthogonally Protected (±)-3-Amino-4-Anilidopiperidines and (±)-3- N -Carbomethoxyfentanyl. Synthesis (Germany) 2017, 49 (14), 3126–3136. https://doi.org/10.1055/s-0036-1588985
UR  - https://hdl.handle.net/21.15107/rcub_cherry_3249
ER  - 

@misc{
author = "Jevtić, Ivana I. and Došen-Mićović, Ljiljana and Ivanović, Evica R. and Todorović, Nina and Ivanović, Milovan",
year = "2017",
publisher = "Georg Thieme Verlag Kg, Stuttgart",
journal = "Synthesis",
title = "Supplementary material for the article: Jevtić, I. I.; Došen-Mićović, L. I.; Ivanović, E. R.; Todorović, N. M.; Ivanović, M. D. Synthesis of Orthogonally Protected (±)-3-Amino-4-Anilidopiperidines and (±)-3- N -Carbomethoxyfentanyl. Synthesis (Germany) 2017, 49 (14), 3126–3136. https://doi.org/10.1055/s-0036-1588985",
url = "https://hdl.handle.net/21.15107/rcub_cherry_3249"
}

Jevtić, I. I., Došen-Mićović, L., Ivanović, E. R., Todorović, N.,& Ivanović, M.. (2017). Supplementary material for the article: Jevtić, I. I.; Došen-Mićović, L. I.; Ivanović, E. R.; Todorović, N. M.; Ivanović, M. D. Synthesis of Orthogonally Protected (±)-3-Amino-4-Anilidopiperidines and (±)-3- N -Carbomethoxyfentanyl. Synthesis (Germany) 2017, 49 (14), 3126–3136. https://doi.org/10.1055/s-0036-1588985. in Synthesis
Georg Thieme Verlag Kg, Stuttgart..
https://hdl.handle.net/21.15107/rcub_cherry_3249

Jevtić II, Došen-Mićović L, Ivanović ER, Todorović N, Ivanović M. Supplementary material for the article: Jevtić, I. I.; Došen-Mićović, L. I.; Ivanović, E. R.; Todorović, N. M.; Ivanović, M. D. Synthesis of Orthogonally Protected (±)-3-Amino-4-Anilidopiperidines and (±)-3- N -Carbomethoxyfentanyl. Synthesis (Germany) 2017, 49 (14), 3126–3136. https://doi.org/10.1055/s-0036-1588985. in Synthesis. 2017;.
https://hdl.handle.net/21.15107/rcub_cherry_3249 .

Jevtić, Ivana I., Došen-Mićović, Ljiljana, Ivanović, Evica R., Todorović, Nina, Ivanović, Milovan, "Supplementary material for the article: Jevtić, I. I.; Došen-Mićović, L. I.; Ivanović, E. R.; Todorović, N. M.; Ivanović, M. D. Synthesis of Orthogonally Protected (±)-3-Amino-4-Anilidopiperidines and (±)-3- N -Carbomethoxyfentanyl. Synthesis (Germany) 2017, 49 (14), 3126–3136. https://doi.org/10.1055/s-0036-1588985" in Synthesis (2017),
https://hdl.handle.net/21.15107/rcub_cherry_3249 .

TY  - JOUR
AU  - Popović-Djordjević, Jelena
AU  - Stepanović, Stepan
AU  - Došen-Mićović, Ljiljana
AU  - Ivanović, Evica R.
AU  - Ivanović, Milovan
PY  - 2016
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/115
AB  - It was found that NaH suspension in DMSO was highly activated when reacted with an alcohol. The in situ generated NaH/alkoxide mixture permitted very rapid and complete deprotonation and acylation of various cyclic ketones with alkyl carbonates at ambient temperature. Activated NaH/alkoxide in DMSO is particularly effective in Dieckmann condensations, where it affords 5- and 6-membered carbocyclic or N-containing heterocyclic β-keto esters in high yields. A heterocyclic Dieckmann condensation was performed on a molar scale, demonstrating the scalability of the procedure. Besides, DMSO is non-toxic, relatively inexpensive and environmentally benign solvent. © 2016 The Author(s). Published by Taylor & Francis.
T2  - Green Chemistry Letters and Reviews
T1  - High-yielding method for preparation of carbocyclic or N-containing heterocyclic β-keto esters using in situ activated sodium hydride in dimethyl sulphoxide
VL  - 9
IS  - 1
SP  - 61
EP  - 68
DO  - 10.1080/17518253.2016.1145744
ER  - 

@article{
author = "Popović-Djordjević, Jelena and Stepanović, Stepan and Došen-Mićović, Ljiljana and Ivanović, Evica R. and Ivanović, Milovan",
year = "2016",
abstract = "It was found that NaH suspension in DMSO was highly activated when reacted with an alcohol. The in situ generated NaH/alkoxide mixture permitted very rapid and complete deprotonation and acylation of various cyclic ketones with alkyl carbonates at ambient temperature. Activated NaH/alkoxide in DMSO is particularly effective in Dieckmann condensations, where it affords 5- and 6-membered carbocyclic or N-containing heterocyclic β-keto esters in high yields. A heterocyclic Dieckmann condensation was performed on a molar scale, demonstrating the scalability of the procedure. Besides, DMSO is non-toxic, relatively inexpensive and environmentally benign solvent. © 2016 The Author(s). Published by Taylor & Francis.",
journal = "Green Chemistry Letters and Reviews",
title = "High-yielding method for preparation of carbocyclic or N-containing heterocyclic β-keto esters using in situ activated sodium hydride in dimethyl sulphoxide",
volume = "9",
number = "1",
pages = "61-68",
doi = "10.1080/17518253.2016.1145744"
}

Popović-Djordjević, J., Stepanović, S., Došen-Mićović, L., Ivanović, E. R.,& Ivanović, M.. (2016). High-yielding method for preparation of carbocyclic or N-containing heterocyclic β-keto esters using in situ activated sodium hydride in dimethyl sulphoxide. in Green Chemistry Letters and Reviews, 9(1), 61-68.
https://doi.org/10.1080/17518253.2016.1145744

Popović-Djordjević J, Stepanović S, Došen-Mićović L, Ivanović ER, Ivanović M. High-yielding method for preparation of carbocyclic or N-containing heterocyclic β-keto esters using in situ activated sodium hydride in dimethyl sulphoxide. in Green Chemistry Letters and Reviews. 2016;9(1):61-68.
doi:10.1080/17518253.2016.1145744 .

Popović-Djordjević, Jelena, Stepanović, Stepan, Došen-Mićović, Ljiljana, Ivanović, Evica R., Ivanović, Milovan, "High-yielding method for preparation of carbocyclic or N-containing heterocyclic β-keto esters using in situ activated sodium hydride in dimethyl sulphoxide" in Green Chemistry Letters and Reviews, 9, no. 1 (2016):61-68,
https://doi.org/10.1080/17518253.2016.1145744 . .

TY  - JOUR
AU  - Popović-Djordjević, Jelena
AU  - Stepanović, Stepan
AU  - Došen-Mićović, Ljiljana
AU  - Ivanović, Evica R.
AU  - Ivanović, Milovan
PY  - 2016
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3522
T2  - Green Chemistry Letters and Reviews
T1  - Supplementary data for the article: Popović-Djordjević, J.; Stepanović, S.; Došen-Mićović, L.; Ivanović, E.; Ivanović, M. D. High-Yielding Method for Preparation of Carbocyclic or N-Containing Heterocyclic β-Keto Esters Using in Situ Activated Sodium Hydride in Dimethyl Sulphoxide. Green Chemistry Letters and Reviews 2016, 9 (1), 61–68. https://doi.org/10.1080/17518253.2016.1145744
UR  - https://hdl.handle.net/21.15107/rcub_cherry_3522
ER  - 

@article{
author = "Popović-Djordjević, Jelena and Stepanović, Stepan and Došen-Mićović, Ljiljana and Ivanović, Evica R. and Ivanović, Milovan",
year = "2016",
journal = "Green Chemistry Letters and Reviews",
title = "Supplementary data for the article: Popović-Djordjević, J.; Stepanović, S.; Došen-Mićović, L.; Ivanović, E.; Ivanović, M. D. High-Yielding Method for Preparation of Carbocyclic or N-Containing Heterocyclic β-Keto Esters Using in Situ Activated Sodium Hydride in Dimethyl Sulphoxide. Green Chemistry Letters and Reviews 2016, 9 (1), 61–68. https://doi.org/10.1080/17518253.2016.1145744",
url = "https://hdl.handle.net/21.15107/rcub_cherry_3522"
}

Popović-Djordjević, J., Stepanović, S., Došen-Mićović, L., Ivanović, E. R.,& Ivanović, M.. (2016). Supplementary data for the article: Popović-Djordjević, J.; Stepanović, S.; Došen-Mićović, L.; Ivanović, E.; Ivanović, M. D. High-Yielding Method for Preparation of Carbocyclic or N-Containing Heterocyclic β-Keto Esters Using in Situ Activated Sodium Hydride in Dimethyl Sulphoxide. Green Chemistry Letters and Reviews 2016, 9 (1), 61–68. https://doi.org/10.1080/17518253.2016.1145744. in Green Chemistry Letters and Reviews.
https://hdl.handle.net/21.15107/rcub_cherry_3522

Popović-Djordjević J, Stepanović S, Došen-Mićović L, Ivanović ER, Ivanović M. Supplementary data for the article: Popović-Djordjević, J.; Stepanović, S.; Došen-Mićović, L.; Ivanović, E.; Ivanović, M. D. High-Yielding Method for Preparation of Carbocyclic or N-Containing Heterocyclic β-Keto Esters Using in Situ Activated Sodium Hydride in Dimethyl Sulphoxide. Green Chemistry Letters and Reviews 2016, 9 (1), 61–68. https://doi.org/10.1080/17518253.2016.1145744. in Green Chemistry Letters and Reviews. 2016;.
https://hdl.handle.net/21.15107/rcub_cherry_3522 .

Popović-Djordjević, Jelena, Stepanović, Stepan, Došen-Mićović, Ljiljana, Ivanović, Evica R., Ivanović, Milovan, "Supplementary data for the article: Popović-Djordjević, J.; Stepanović, S.; Došen-Mićović, L.; Ivanović, E.; Ivanović, M. D. High-Yielding Method for Preparation of Carbocyclic or N-Containing Heterocyclic β-Keto Esters Using in Situ Activated Sodium Hydride in Dimethyl Sulphoxide. Green Chemistry Letters and Reviews 2016, 9 (1), 61–68. https://doi.org/10.1080/17518253.2016.1145744" in Green Chemistry Letters and Reviews (2016),
https://hdl.handle.net/21.15107/rcub_cherry_3522 .

TY  - JOUR
AU  - Jevtić, Ivana I.
AU  - Došen-Mićović, Ljiljana
AU  - Ivanović, Evica R.
AU  - Ivanović, Milovan
PY  - 2016
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1935
AB  - An efficient, one-pot procedure for the Hofmann rearrangement of aromatic and aliphatic amides has been developed. Methyl and benzyl carbamates are produced with N-bromoacetamide in the presence of lithium hydroxide or lithium methoxide, in high yields. -Phenylamino amides gave five-membered cyclic ureas stereospecifically. Side products of aryl or benzyl bromination were minimized. This procedure offers an easy access to various protected amines or diamines, which represent important synthetic precursors.
PB  - Georg Thieme Verlag Kg, Stuttgart
T2  - Synthesis, Stuttgart
T1  - Hofmann Rearrangement of Carboxamides Mediated by N-Bromoacetamide
VL  - 48
IS  - 10
SP  - 1550
EP  - 1560
DO  - 10.1055/s-0035-1561405
ER  - 

@article{
author = "Jevtić, Ivana I. and Došen-Mićović, Ljiljana and Ivanović, Evica R. and Ivanović, Milovan",
year = "2016",
abstract = "An efficient, one-pot procedure for the Hofmann rearrangement of aromatic and aliphatic amides has been developed. Methyl and benzyl carbamates are produced with N-bromoacetamide in the presence of lithium hydroxide or lithium methoxide, in high yields. -Phenylamino amides gave five-membered cyclic ureas stereospecifically. Side products of aryl or benzyl bromination were minimized. This procedure offers an easy access to various protected amines or diamines, which represent important synthetic precursors.",
publisher = "Georg Thieme Verlag Kg, Stuttgart",
journal = "Synthesis, Stuttgart",
title = "Hofmann Rearrangement of Carboxamides Mediated by N-Bromoacetamide",
volume = "48",
number = "10",
pages = "1550-1560",
doi = "10.1055/s-0035-1561405"
}

Jevtić, I. I., Došen-Mićović, L., Ivanović, E. R.,& Ivanović, M.. (2016). Hofmann Rearrangement of Carboxamides Mediated by N-Bromoacetamide. in Synthesis, Stuttgart
Georg Thieme Verlag Kg, Stuttgart., 48(10), 1550-1560.
https://doi.org/10.1055/s-0035-1561405

Jevtić II, Došen-Mićović L, Ivanović ER, Ivanović M. Hofmann Rearrangement of Carboxamides Mediated by N-Bromoacetamide. in Synthesis, Stuttgart. 2016;48(10):1550-1560.
doi:10.1055/s-0035-1561405 .

Jevtić, Ivana I., Došen-Mićović, Ljiljana, Ivanović, Evica R., Ivanović, Milovan, "Hofmann Rearrangement of Carboxamides Mediated by N-Bromoacetamide" in Synthesis, Stuttgart, 48, no. 10 (2016):1550-1560,
https://doi.org/10.1055/s-0035-1561405 . .

TY  - DATA
AU  - Jevtić, Ivana I.
AU  - Došen-Mićović, Ljiljana
AU  - Ivanović, Evica R.
AU  - Ivanović, Milovan
PY  - 2016
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3523
PB  - Georg Thieme Verlag Kg, Stuttgart
T2  - Synthesis, Stuttgart
T1  - Supplementary data for the article: Jevtić, I. I.; Došen-Mićović, L.; Ivanović, E. R.; Ivanović, M. D. Hofmann Rearrangement of Carboxamides Mediated by N-Bromoacetamide. Synthesis (Germany) 2016, 48 (10), 1550–1560. https://doi.org/10.1055/s-0035-1561405
UR  - https://hdl.handle.net/21.15107/rcub_cherry_3523
ER  - 

@misc{
author = "Jevtić, Ivana I. and Došen-Mićović, Ljiljana and Ivanović, Evica R. and Ivanović, Milovan",
year = "2016",
publisher = "Georg Thieme Verlag Kg, Stuttgart",
journal = "Synthesis, Stuttgart",
title = "Supplementary data for the article: Jevtić, I. I.; Došen-Mićović, L.; Ivanović, E. R.; Ivanović, M. D. Hofmann Rearrangement of Carboxamides Mediated by N-Bromoacetamide. Synthesis (Germany) 2016, 48 (10), 1550–1560. https://doi.org/10.1055/s-0035-1561405",
url = "https://hdl.handle.net/21.15107/rcub_cherry_3523"
}

Jevtić, I. I., Došen-Mićović, L., Ivanović, E. R.,& Ivanović, M.. (2016). Supplementary data for the article: Jevtić, I. I.; Došen-Mićović, L.; Ivanović, E. R.; Ivanović, M. D. Hofmann Rearrangement of Carboxamides Mediated by N-Bromoacetamide. Synthesis (Germany) 2016, 48 (10), 1550–1560. https://doi.org/10.1055/s-0035-1561405. in Synthesis, Stuttgart
Georg Thieme Verlag Kg, Stuttgart..
https://hdl.handle.net/21.15107/rcub_cherry_3523

Jevtić II, Došen-Mićović L, Ivanović ER, Ivanović M. Supplementary data for the article: Jevtić, I. I.; Došen-Mićović, L.; Ivanović, E. R.; Ivanović, M. D. Hofmann Rearrangement of Carboxamides Mediated by N-Bromoacetamide. Synthesis (Germany) 2016, 48 (10), 1550–1560. https://doi.org/10.1055/s-0035-1561405. in Synthesis, Stuttgart. 2016;.
https://hdl.handle.net/21.15107/rcub_cherry_3523 .

Jevtić, Ivana I., Došen-Mićović, Ljiljana, Ivanović, Evica R., Ivanović, Milovan, "Supplementary data for the article: Jevtić, I. I.; Došen-Mićović, L.; Ivanović, E. R.; Ivanović, M. D. Hofmann Rearrangement of Carboxamides Mediated by N-Bromoacetamide. Synthesis (Germany) 2016, 48 (10), 1550–1560. https://doi.org/10.1055/s-0035-1561405" in Synthesis, Stuttgart (2016),
https://hdl.handle.net/21.15107/rcub_cherry_3523 .