TY  - JOUR
AU  - Xie, Yun
AU  - Ilic, Stefan
AU  - Škaro, Sanja
AU  - Maslak, Veselin
AU  - Glušač, Ksenija D.
PY  - 2017
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2977
AB  - The excited-state heterolysis of acridinol-based derivatives leads to the release of the OH- ion and the formation of the corresponding acridinium cations. To evaluate the parameters that control the reaction barriers, the kinetics of excited-state OH- release from a series of acridinol photobases were studied using transient absorption spectroscopy. The rate constants were obtained in three solvents (methanol, butanol, and isobutanol), and the data were modeled using Marcus theory. The intrinsic reorganization energies obtained from these fits were found to correlate well with the solvent reorganization energies calculated using dielectric continuum model, suggesting that the excited-state OH- release occurs along the solvent reaction coordinate. Furthermore, the ability of acridinol photobases to photoinitiate chemical reactions was demonstrated using the Michael reaction between dimethylmalonate and nitrostyrene.
PB  - Amer Chemical Soc, Washington
T2  - Journal of Physical Chemistry. Part A: Molecules, Spectroscopy, Kinetics, Environment and General Theory
T1  - Excited-State Hydroxide Ion Release From a Series of Acridinol Photobases
VL  - 121
IS  - 2
SP  - 448
EP  - 457
DO  - 10.1021/acs.jpca.6b10980
ER  - 

@article{
author = "Xie, Yun and Ilic, Stefan and Škaro, Sanja and Maslak, Veselin and Glušač, Ksenija D.",
year = "2017",
abstract = "The excited-state heterolysis of acridinol-based derivatives leads to the release of the OH- ion and the formation of the corresponding acridinium cations. To evaluate the parameters that control the reaction barriers, the kinetics of excited-state OH- release from a series of acridinol photobases were studied using transient absorption spectroscopy. The rate constants were obtained in three solvents (methanol, butanol, and isobutanol), and the data were modeled using Marcus theory. The intrinsic reorganization energies obtained from these fits were found to correlate well with the solvent reorganization energies calculated using dielectric continuum model, suggesting that the excited-state OH- release occurs along the solvent reaction coordinate. Furthermore, the ability of acridinol photobases to photoinitiate chemical reactions was demonstrated using the Michael reaction between dimethylmalonate and nitrostyrene.",
publisher = "Amer Chemical Soc, Washington",
journal = "Journal of Physical Chemistry. Part A: Molecules, Spectroscopy, Kinetics, Environment and General Theory",
title = "Excited-State Hydroxide Ion Release From a Series of Acridinol Photobases",
volume = "121",
number = "2",
pages = "448-457",
doi = "10.1021/acs.jpca.6b10980"
}

Xie, Y., Ilic, S., Škaro, S., Maslak, V.,& Glušač, K. D.. (2017). Excited-State Hydroxide Ion Release From a Series of Acridinol Photobases. in Journal of Physical Chemistry. Part A: Molecules, Spectroscopy, Kinetics, Environment and General Theory
Amer Chemical Soc, Washington., 121(2), 448-457.
https://doi.org/10.1021/acs.jpca.6b10980

Xie Y, Ilic S, Škaro S, Maslak V, Glušač KD. Excited-State Hydroxide Ion Release From a Series of Acridinol Photobases. in Journal of Physical Chemistry. Part A: Molecules, Spectroscopy, Kinetics, Environment and General Theory. 2017;121(2):448-457.
doi:10.1021/acs.jpca.6b10980 .

Xie, Yun, Ilic, Stefan, Škaro, Sanja, Maslak, Veselin, Glušač, Ksenija D., "Excited-State Hydroxide Ion Release From a Series of Acridinol Photobases" in Journal of Physical Chemistry. Part A: Molecules, Spectroscopy, Kinetics, Environment and General Theory, 121, no. 2 (2017):448-457,
https://doi.org/10.1021/acs.jpca.6b10980 . .

TY  - JOUR
AU  - Xie, Yun
AU  - Ilic, Stefan
AU  - Škaro, Sanja
AU  - Maslak, Veselin
AU  - Glušač, Ksenija D.
PY  - 2017
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2382
AB  - The excited-state heterolysis of acridinol-based derivatives leads to the release of the OH- ion and the formation of the corresponding acridinium cations. To evaluate the parameters that control the reaction barriers, the kinetics of excited-state OH- release from a series of acridinol photobases were studied using transient absorption spectroscopy. The rate constants were obtained in three solvents (methanol, butanol, and isobutanol), and the data were modeled using Marcus theory. The intrinsic reorganization energies obtained from these fits were found to correlate well with the solvent reorganization energies calculated using dielectric continuum model, suggesting that the excited-state OH- release occurs along the solvent reaction coordinate. Furthermore, the ability of acridinol photobases to photoinitiate chemical reactions was demonstrated using the Michael reaction between dimethylmalonate and nitrostyrene.
PB  - Amer Chemical Soc, Washington
T2  - Journal of Physical Chemistry. Part A: Molecules, Spectroscopy, Kinetics, Environment and General Th
T1  - Excited-State Hydroxide Ion Release From a Series of Acridinol Photobases
VL  - 121
IS  - 2
SP  - 448
EP  - 457
DO  - 10.1021/acs.jpca.6b10980
ER  - 

@article{
author = "Xie, Yun and Ilic, Stefan and Škaro, Sanja and Maslak, Veselin and Glušač, Ksenija D.",
year = "2017",
abstract = "The excited-state heterolysis of acridinol-based derivatives leads to the release of the OH- ion and the formation of the corresponding acridinium cations. To evaluate the parameters that control the reaction barriers, the kinetics of excited-state OH- release from a series of acridinol photobases were studied using transient absorption spectroscopy. The rate constants were obtained in three solvents (methanol, butanol, and isobutanol), and the data were modeled using Marcus theory. The intrinsic reorganization energies obtained from these fits were found to correlate well with the solvent reorganization energies calculated using dielectric continuum model, suggesting that the excited-state OH- release occurs along the solvent reaction coordinate. Furthermore, the ability of acridinol photobases to photoinitiate chemical reactions was demonstrated using the Michael reaction between dimethylmalonate and nitrostyrene.",
publisher = "Amer Chemical Soc, Washington",
journal = "Journal of Physical Chemistry. Part A: Molecules, Spectroscopy, Kinetics, Environment and General Th",
title = "Excited-State Hydroxide Ion Release From a Series of Acridinol Photobases",
volume = "121",
number = "2",
pages = "448-457",
doi = "10.1021/acs.jpca.6b10980"
}

Xie, Y., Ilic, S., Škaro, S., Maslak, V.,& Glušač, K. D.. (2017). Excited-State Hydroxide Ion Release From a Series of Acridinol Photobases. in Journal of Physical Chemistry. Part A: Molecules, Spectroscopy, Kinetics, Environment and General Th
Amer Chemical Soc, Washington., 121(2), 448-457.
https://doi.org/10.1021/acs.jpca.6b10980

Xie Y, Ilic S, Škaro S, Maslak V, Glušač KD. Excited-State Hydroxide Ion Release From a Series of Acridinol Photobases. in Journal of Physical Chemistry. Part A: Molecules, Spectroscopy, Kinetics, Environment and General Th. 2017;121(2):448-457.
doi:10.1021/acs.jpca.6b10980 .

Xie, Yun, Ilic, Stefan, Škaro, Sanja, Maslak, Veselin, Glušač, Ksenija D., "Excited-State Hydroxide Ion Release From a Series of Acridinol Photobases" in Journal of Physical Chemistry. Part A: Molecules, Spectroscopy, Kinetics, Environment and General Th, 121, no. 2 (2017):448-457,
https://doi.org/10.1021/acs.jpca.6b10980 . .

TY  - DATA
AU  - Radivojević, Jelena
AU  - Škaro, Sanja
AU  - Šenerović, Lidija
AU  - Vasiljević, Branka
AU  - Guzik, Maciej
AU  - Kenny, Shane T.
AU  - Maslak, Veselin
AU  - Nikodinović-Runić, Jasmina
AU  - O'Connor, Kevin E.
PY  - 2016
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3595
PB  - Springer, New York
T2  - Applied Microbiology and Biotechnology
T1  - Supplementary data for the article: Radivojevic, J.; Skaro, S.; Senerovic, L.; Vasiljevic, B.; Guzik, M.; Kenny, S. T.; Maslak, V.; Nikodinovic-Runic, J.; O’Connor, K. E. Polyhydroxyalkanoate-Based 3-Hydroxyoctanoic Acid and Its Derivatives as a Platform of Bioactive Compounds. Applied Microbiology and Biotechnology 2016, 100 (1), 161–172. https://doi.org/10.1007/s00253-015-6984-4
UR  - https://hdl.handle.net/21.15107/rcub_cherry_3595
ER  - 

@misc{
author = "Radivojević, Jelena and Škaro, Sanja and Šenerović, Lidija and Vasiljević, Branka and Guzik, Maciej and Kenny, Shane T. and Maslak, Veselin and Nikodinović-Runić, Jasmina and O'Connor, Kevin E.",
year = "2016",
publisher = "Springer, New York",
journal = "Applied Microbiology and Biotechnology",
title = "Supplementary data for the article: Radivojevic, J.; Skaro, S.; Senerovic, L.; Vasiljevic, B.; Guzik, M.; Kenny, S. T.; Maslak, V.; Nikodinovic-Runic, J.; O’Connor, K. E. Polyhydroxyalkanoate-Based 3-Hydroxyoctanoic Acid and Its Derivatives as a Platform of Bioactive Compounds. Applied Microbiology and Biotechnology 2016, 100 (1), 161–172. https://doi.org/10.1007/s00253-015-6984-4",
url = "https://hdl.handle.net/21.15107/rcub_cherry_3595"
}

Radivojević, J., Škaro, S., Šenerović, L., Vasiljević, B., Guzik, M., Kenny, S. T., Maslak, V., Nikodinović-Runić, J.,& O'Connor, K. E.. (2016). Supplementary data for the article: Radivojevic, J.; Skaro, S.; Senerovic, L.; Vasiljevic, B.; Guzik, M.; Kenny, S. T.; Maslak, V.; Nikodinovic-Runic, J.; O’Connor, K. E. Polyhydroxyalkanoate-Based 3-Hydroxyoctanoic Acid and Its Derivatives as a Platform of Bioactive Compounds. Applied Microbiology and Biotechnology 2016, 100 (1), 161–172. https://doi.org/10.1007/s00253-015-6984-4. in Applied Microbiology and Biotechnology
Springer, New York..
https://hdl.handle.net/21.15107/rcub_cherry_3595

Radivojević J, Škaro S, Šenerović L, Vasiljević B, Guzik M, Kenny ST, Maslak V, Nikodinović-Runić J, O'Connor KE. Supplementary data for the article: Radivojevic, J.; Skaro, S.; Senerovic, L.; Vasiljevic, B.; Guzik, M.; Kenny, S. T.; Maslak, V.; Nikodinovic-Runic, J.; O’Connor, K. E. Polyhydroxyalkanoate-Based 3-Hydroxyoctanoic Acid and Its Derivatives as a Platform of Bioactive Compounds. Applied Microbiology and Biotechnology 2016, 100 (1), 161–172. https://doi.org/10.1007/s00253-015-6984-4. in Applied Microbiology and Biotechnology. 2016;.
https://hdl.handle.net/21.15107/rcub_cherry_3595 .

Radivojević, Jelena, Škaro, Sanja, Šenerović, Lidija, Vasiljević, Branka, Guzik, Maciej, Kenny, Shane T., Maslak, Veselin, Nikodinović-Runić, Jasmina, O'Connor, Kevin E., "Supplementary data for the article: Radivojevic, J.; Skaro, S.; Senerovic, L.; Vasiljevic, B.; Guzik, M.; Kenny, S. T.; Maslak, V.; Nikodinovic-Runic, J.; O’Connor, K. E. Polyhydroxyalkanoate-Based 3-Hydroxyoctanoic Acid and Its Derivatives as a Platform of Bioactive Compounds. Applied Microbiology and Biotechnology 2016, 100 (1), 161–172. https://doi.org/10.1007/s00253-015-6984-4" in Applied Microbiology and Biotechnology (2016),
https://hdl.handle.net/21.15107/rcub_cherry_3595 .

TY  - JOUR
AU  - Radivojević, Jelena
AU  - Škaro, Sanja
AU  - Šenerović, Lidija
AU  - Vasiljević, Branka
AU  - Guzik, Maciej
AU  - Kenny, Shane T.
AU  - Maslak, Veselin
AU  - Nikodinović-Runić, Jasmina
AU  - O'Connor, Kevin E.
PY  - 2016
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2025
AB  - A library of 18 different compounds was synthesized starting from (R)-3-hydroxyoctanoic acid which is derived from the bacterial polymer polyhydroxyalkanoate (PHA). Ten derivatives, including halo and unsaturated methyl and benzyl esters, were synthesized and characterized for the first time. Given that (R)-3-hydroxyalkanoic acids are known to have biological activity, the new compounds were evaluated for antimicrobial activity and in vitro antiproliferative effect with mammalian cell lines. The presence of the carboxylic group was essential for the antimicrobial activity, with minimal inhibitory concentrations against a panel of bacteria (Gram-positive and Gram-negative) and fungi (Candida albicans and Microsporum gypseum) in the range 2.8-7.0 mM and 0.1-6.3 mM, respectively. 3-Halogenated octanoic acids exhibited the ability to inhibit C. albicans hyphae formation. In addition, (R)-3-hydroxyoctanoic and (E)-oct-2-enoic acids inhibited quorum sensing-regulated pyocyanin production in the opportunistic pathogen Pseudomonas aeruginosa PAO1. Generally, derivatives did not inhibit mammalian cell proliferation even at 3-mM concentrations, while only (E)-oct-2-enoic and 3-oxooctanoic acid had IC50 values of 1.7 and 1.6 mM with the human lung fibroblast cell line.
PB  - Springer, New York
T2  - Applied Microbiology and Biotechnology
T1  - Polyhydroxyalkanoate-based 3-hydroxyoctanoic acid and its derivatives as a platform of bioactive compounds
VL  - 100
IS  - 1
SP  - 161
EP  - 172
DO  - 10.1007/s00253-015-6984-4
ER  - 

@article{
author = "Radivojević, Jelena and Škaro, Sanja and Šenerović, Lidija and Vasiljević, Branka and Guzik, Maciej and Kenny, Shane T. and Maslak, Veselin and Nikodinović-Runić, Jasmina and O'Connor, Kevin E.",
year = "2016",
abstract = "A library of 18 different compounds was synthesized starting from (R)-3-hydroxyoctanoic acid which is derived from the bacterial polymer polyhydroxyalkanoate (PHA). Ten derivatives, including halo and unsaturated methyl and benzyl esters, were synthesized and characterized for the first time. Given that (R)-3-hydroxyalkanoic acids are known to have biological activity, the new compounds were evaluated for antimicrobial activity and in vitro antiproliferative effect with mammalian cell lines. The presence of the carboxylic group was essential for the antimicrobial activity, with minimal inhibitory concentrations against a panel of bacteria (Gram-positive and Gram-negative) and fungi (Candida albicans and Microsporum gypseum) in the range 2.8-7.0 mM and 0.1-6.3 mM, respectively. 3-Halogenated octanoic acids exhibited the ability to inhibit C. albicans hyphae formation. In addition, (R)-3-hydroxyoctanoic and (E)-oct-2-enoic acids inhibited quorum sensing-regulated pyocyanin production in the opportunistic pathogen Pseudomonas aeruginosa PAO1. Generally, derivatives did not inhibit mammalian cell proliferation even at 3-mM concentrations, while only (E)-oct-2-enoic and 3-oxooctanoic acid had IC50 values of 1.7 and 1.6 mM with the human lung fibroblast cell line.",
publisher = "Springer, New York",
journal = "Applied Microbiology and Biotechnology",
title = "Polyhydroxyalkanoate-based 3-hydroxyoctanoic acid and its derivatives as a platform of bioactive compounds",
volume = "100",
number = "1",
pages = "161-172",
doi = "10.1007/s00253-015-6984-4"
}

Radivojević, J., Škaro, S., Šenerović, L., Vasiljević, B., Guzik, M., Kenny, S. T., Maslak, V., Nikodinović-Runić, J.,& O'Connor, K. E.. (2016). Polyhydroxyalkanoate-based 3-hydroxyoctanoic acid and its derivatives as a platform of bioactive compounds. in Applied Microbiology and Biotechnology
Springer, New York., 100(1), 161-172.
https://doi.org/10.1007/s00253-015-6984-4

Radivojević J, Škaro S, Šenerović L, Vasiljević B, Guzik M, Kenny ST, Maslak V, Nikodinović-Runić J, O'Connor KE. Polyhydroxyalkanoate-based 3-hydroxyoctanoic acid and its derivatives as a platform of bioactive compounds. in Applied Microbiology and Biotechnology. 2016;100(1):161-172.
doi:10.1007/s00253-015-6984-4 .

Radivojević, Jelena, Škaro, Sanja, Šenerović, Lidija, Vasiljević, Branka, Guzik, Maciej, Kenny, Shane T., Maslak, Veselin, Nikodinović-Runić, Jasmina, O'Connor, Kevin E., "Polyhydroxyalkanoate-based 3-hydroxyoctanoic acid and its derivatives as a platform of bioactive compounds" in Applied Microbiology and Biotechnology, 100, no. 1 (2016):161-172,
https://doi.org/10.1007/s00253-015-6984-4 . .

TY  - DATA
AU  - Bigović, Miljan
AU  - Škaro, Sanja
AU  - Maslak, Veselin
AU  - Saičić, Radomir
PY  - 2013
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3493
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Tetrahedron Letters
T1  - Supplementary data for article: Bigović, M.; Skaro, S.; Maslak, V.; Saičić, R. Expanding the Scope of the Indium-Promoted Allylation Reaction: 4-(Bromomethyl)-1,3-Dioxol-2-One as a Synthetic Equivalent of a 3-Arylhydroxyacetone Enolate. Tetrahedron Letters 2013, 54 (48), 6624–6626. https://doi.org/10.1016/j.tetlet.2013.09.115eaction: 4-(bromomethyl)-1,3-dioxol-2-one as a synthetic equivalent of a 3-arylhydroxyacetone enolate
UR  - https://hdl.handle.net/21.15107/rcub_cherry_3493
ER  - 

@misc{
author = "Bigović, Miljan and Škaro, Sanja and Maslak, Veselin and Saičić, Radomir",
year = "2013",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Tetrahedron Letters",
title = "Supplementary data for article: Bigović, M.; Skaro, S.; Maslak, V.; Saičić, R. Expanding the Scope of the Indium-Promoted Allylation Reaction: 4-(Bromomethyl)-1,3-Dioxol-2-One as a Synthetic Equivalent of a 3-Arylhydroxyacetone Enolate. Tetrahedron Letters 2013, 54 (48), 6624–6626. https://doi.org/10.1016/j.tetlet.2013.09.115eaction: 4-(bromomethyl)-1,3-dioxol-2-one as a synthetic equivalent of a 3-arylhydroxyacetone enolate",
url = "https://hdl.handle.net/21.15107/rcub_cherry_3493"
}

Bigović, M., Škaro, S., Maslak, V.,& Saičić, R.. (2013). Supplementary data for article: Bigović, M.; Skaro, S.; Maslak, V.; Saičić, R. Expanding the Scope of the Indium-Promoted Allylation Reaction: 4-(Bromomethyl)-1,3-Dioxol-2-One as a Synthetic Equivalent of a 3-Arylhydroxyacetone Enolate. Tetrahedron Letters 2013, 54 (48), 6624–6626. https://doi.org/10.1016/j.tetlet.2013.09.115eaction: 4-(bromomethyl)-1,3-dioxol-2-one as a synthetic equivalent of a 3-arylhydroxyacetone enolate. in Tetrahedron Letters
Pergamon-Elsevier Science Ltd, Oxford..
https://hdl.handle.net/21.15107/rcub_cherry_3493

Bigović M, Škaro S, Maslak V, Saičić R. Supplementary data for article: Bigović, M.; Skaro, S.; Maslak, V.; Saičić, R. Expanding the Scope of the Indium-Promoted Allylation Reaction: 4-(Bromomethyl)-1,3-Dioxol-2-One as a Synthetic Equivalent of a 3-Arylhydroxyacetone Enolate. Tetrahedron Letters 2013, 54 (48), 6624–6626. https://doi.org/10.1016/j.tetlet.2013.09.115eaction: 4-(bromomethyl)-1,3-dioxol-2-one as a synthetic equivalent of a 3-arylhydroxyacetone enolate. in Tetrahedron Letters. 2013;.
https://hdl.handle.net/21.15107/rcub_cherry_3493 .

Bigović, Miljan, Škaro, Sanja, Maslak, Veselin, Saičić, Radomir, "Supplementary data for article: Bigović, M.; Skaro, S.; Maslak, V.; Saičić, R. Expanding the Scope of the Indium-Promoted Allylation Reaction: 4-(Bromomethyl)-1,3-Dioxol-2-One as a Synthetic Equivalent of a 3-Arylhydroxyacetone Enolate. Tetrahedron Letters 2013, 54 (48), 6624–6626. https://doi.org/10.1016/j.tetlet.2013.09.115eaction: 4-(bromomethyl)-1,3-dioxol-2-one as a synthetic equivalent of a 3-arylhydroxyacetone enolate" in Tetrahedron Letters (2013),
https://hdl.handle.net/21.15107/rcub_cherry_3493 .

TY  - JOUR
AU  - Bigović, Miljan
AU  - Škaro, Sanja
AU  - Maslak, Veselin
AU  - Saičić, Radomir
PY  - 2013
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1430
AB  - Cyclic enol carbonates of type 2, obtained via the indium-promoted allylation of aldehydes with 4-(bromomethyl)-1,3-dioxol-2-one, undergo Heck reaction with aryl iodides in the presence of silver trifluoroacetate, to give the corresponding arylated products. Thus, 4-(bromomethyl)-1,3-dioxol-2-one can be considered as a synthetic equivalent of 3-mylhydroxyacetone enolate.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Tetrahedron Letters
T1  - Expanding the scope of the indium-promoted allylation reaction: 4-(bromomethyl)-1,3-dioxol-2-one as a synthetic equivalent of a 3-arylhydroxyacetone enolate
VL  - 54
IS  - 48
SP  - 6624
EP  - 6626
DO  - 10.1016/j.tetlet.2013.09.115
ER  - 

@article{
author = "Bigović, Miljan and Škaro, Sanja and Maslak, Veselin and Saičić, Radomir",
year = "2013",
abstract = "Cyclic enol carbonates of type 2, obtained via the indium-promoted allylation of aldehydes with 4-(bromomethyl)-1,3-dioxol-2-one, undergo Heck reaction with aryl iodides in the presence of silver trifluoroacetate, to give the corresponding arylated products. Thus, 4-(bromomethyl)-1,3-dioxol-2-one can be considered as a synthetic equivalent of 3-mylhydroxyacetone enolate.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Tetrahedron Letters",
title = "Expanding the scope of the indium-promoted allylation reaction: 4-(bromomethyl)-1,3-dioxol-2-one as a synthetic equivalent of a 3-arylhydroxyacetone enolate",
volume = "54",
number = "48",
pages = "6624-6626",
doi = "10.1016/j.tetlet.2013.09.115"
}

Bigović, M., Škaro, S., Maslak, V.,& Saičić, R.. (2013). Expanding the scope of the indium-promoted allylation reaction: 4-(bromomethyl)-1,3-dioxol-2-one as a synthetic equivalent of a 3-arylhydroxyacetone enolate. in Tetrahedron Letters
Pergamon-Elsevier Science Ltd, Oxford., 54(48), 6624-6626.
https://doi.org/10.1016/j.tetlet.2013.09.115

Bigović M, Škaro S, Maslak V, Saičić R. Expanding the scope of the indium-promoted allylation reaction: 4-(bromomethyl)-1,3-dioxol-2-one as a synthetic equivalent of a 3-arylhydroxyacetone enolate. in Tetrahedron Letters. 2013;54(48):6624-6626.
doi:10.1016/j.tetlet.2013.09.115 .

Bigović, Miljan, Škaro, Sanja, Maslak, Veselin, Saičić, Radomir, "Expanding the scope of the indium-promoted allylation reaction: 4-(bromomethyl)-1,3-dioxol-2-one as a synthetic equivalent of a 3-arylhydroxyacetone enolate" in Tetrahedron Letters, 54, no. 48 (2013):6624-6626,
https://doi.org/10.1016/j.tetlet.2013.09.115 . .