TY  - JOUR
AU  - Ferjancic, Zorana
AU  - Bihelovic, Filip
AU  - Vulovic, Bojan
AU  - Matovic, Radomir
AU  - Trmcic, Milena
AU  - Jankovic, Aleksandar
AU  - Pavlovic, Milos
AU  - Djurkovic, Filip
AU  - Prodanovic, Radivoje
AU  - Djurdjevic Djelmas, Aleksandra
AU  - Kalicanin, Nevena
AU  - Zlatovic, Mario
AU  - Sladic, Dusan
AU  - Vallet, Thomas
AU  - Vignuzzi, Marco
AU  - Saicic, Radomir N.
PY  - 2024
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/6475
AB  - We developed new iminosugar-based glycosidase inhibitors against SARS-CoV-2. Known drugs (miglustat, migalastat, miglitol, and swainsonine) were chosen as lead compounds to develop three classes of glycosidase inhibitors (α-glucosidase, α-galactosidase, and mannosidase). Molecular modelling of the lead compounds, synthesis of the compounds with the highest docking scores, enzyme inhibition tests, and in vitro antiviral assays afforded rationally designed inhibitors. Two highly active α-glucosidase inhibitors were discovered, where one of them is the most potent iminosugar-based anti-SARS-CoV-2 agent to date (EC90 = 1.94 µM in A549-ACE2 cells against Omicron BA.1 strain). However, galactosidase inhibitors did not exhibit antiviral activity, whereas mannosidase inhibitors were both active and cytotoxic. As our iminosugar-based drug candidates act by a host-directed mechanism, they should be more resilient to drug resistance. Moreover, this strategy could be extended to identify potential drug candidates for other viral infections.
PB  - Taylor and Francis Group
T2  - Journal of Enzyme Inhibition and Medicinal Chemistry
T1  - Development of iminosugar-based glycosidase inhibitors as drug candidates for SARS-CoV-2 virus via molecular modelling and in vitro studies
VL  - 39
IS  - 1
SP  - 2289007
DO  - 10.1080/14756366.2023.2289007
ER  - 

@article{
author = "Ferjancic, Zorana and Bihelovic, Filip and Vulovic, Bojan and Matovic, Radomir and Trmcic, Milena and Jankovic, Aleksandar and Pavlovic, Milos and Djurkovic, Filip and Prodanovic, Radivoje and Djurdjevic Djelmas, Aleksandra and Kalicanin, Nevena and Zlatovic, Mario and Sladic, Dusan and Vallet, Thomas and Vignuzzi, Marco and Saicic, Radomir N.",
year = "2024",
abstract = "We developed new iminosugar-based glycosidase inhibitors against SARS-CoV-2. Known drugs (miglustat, migalastat, miglitol, and swainsonine) were chosen as lead compounds to develop three classes of glycosidase inhibitors (α-glucosidase, α-galactosidase, and mannosidase). Molecular modelling of the lead compounds, synthesis of the compounds with the highest docking scores, enzyme inhibition tests, and in vitro antiviral assays afforded rationally designed inhibitors. Two highly active α-glucosidase inhibitors were discovered, where one of them is the most potent iminosugar-based anti-SARS-CoV-2 agent to date (EC90 = 1.94 µM in A549-ACE2 cells against Omicron BA.1 strain). However, galactosidase inhibitors did not exhibit antiviral activity, whereas mannosidase inhibitors were both active and cytotoxic. As our iminosugar-based drug candidates act by a host-directed mechanism, they should be more resilient to drug resistance. Moreover, this strategy could be extended to identify potential drug candidates for other viral infections.",
publisher = "Taylor and Francis Group",
journal = "Journal of Enzyme Inhibition and Medicinal Chemistry",
title = "Development of iminosugar-based glycosidase inhibitors as drug candidates for SARS-CoV-2 virus via molecular modelling and in vitro studies",
volume = "39",
number = "1",
pages = "2289007",
doi = "10.1080/14756366.2023.2289007"
}

Ferjancic, Z., Bihelovic, F., Vulovic, B., Matovic, R., Trmcic, M., Jankovic, A., Pavlovic, M., Djurkovic, F., Prodanovic, R., Djurdjevic Djelmas, A., Kalicanin, N., Zlatovic, M., Sladic, D., Vallet, T., Vignuzzi, M.,& Saicic, R. N.. (2024). Development of iminosugar-based glycosidase inhibitors as drug candidates for SARS-CoV-2 virus via molecular modelling and in vitro studies. in Journal of Enzyme Inhibition and Medicinal Chemistry
Taylor and Francis Group., 39(1), 2289007.
https://doi.org/10.1080/14756366.2023.2289007

Ferjancic Z, Bihelovic F, Vulovic B, Matovic R, Trmcic M, Jankovic A, Pavlovic M, Djurkovic F, Prodanovic R, Djurdjevic Djelmas A, Kalicanin N, Zlatovic M, Sladic D, Vallet T, Vignuzzi M, Saicic RN. Development of iminosugar-based glycosidase inhibitors as drug candidates for SARS-CoV-2 virus via molecular modelling and in vitro studies. in Journal of Enzyme Inhibition and Medicinal Chemistry. 2024;39(1):2289007.
doi:10.1080/14756366.2023.2289007 .

Ferjancic, Zorana, Bihelovic, Filip, Vulovic, Bojan, Matovic, Radomir, Trmcic, Milena, Jankovic, Aleksandar, Pavlovic, Milos, Djurkovic, Filip, Prodanovic, Radivoje, Djurdjevic Djelmas, Aleksandra, Kalicanin, Nevena, Zlatovic, Mario, Sladic, Dusan, Vallet, Thomas, Vignuzzi, Marco, Saicic, Radomir N., "Development of iminosugar-based glycosidase inhibitors as drug candidates for SARS-CoV-2 virus via molecular modelling and in vitro studies" in Journal of Enzyme Inhibition and Medicinal Chemistry, 39, no. 1 (2024):2289007,
https://doi.org/10.1080/14756366.2023.2289007 . .

TY  - JOUR
AU  - Stjepanovic, Mihailo
AU  - Janković, Aleksandar
AU  - Vulović, Bojan
AU  - Matović, Radomir
AU  - Saičić, Radomir
PY  - 2023
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/6389
AB  - The synthesis of an angular triquinane, which could serve as a suit­able platform for the synthesis of several natural products (panaginsene, sil­phi­nene, senoxydene) is described. The synthesis is based on two consecutive cyc­lo­pentene annulations, where alkenes were used as latent carbonyl function­alities (via Wacker reaction), and cyclopentenone annulation was effected by aldol condensation.
PB  - Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Synthetic study on the angular triquinanes: Scientific paper
VL  - 88
IS  - 10
SP  - 975
EP  - 983
DO  - 10.2298/JSC230627046S
ER  - 

@article{
author = "Stjepanovic, Mihailo and Janković, Aleksandar and Vulović, Bojan and Matović, Radomir and Saičić, Radomir",
year = "2023",
abstract = "The synthesis of an angular triquinane, which could serve as a suit­able platform for the synthesis of several natural products (panaginsene, sil­phi­nene, senoxydene) is described. The synthesis is based on two consecutive cyc­lo­pentene annulations, where alkenes were used as latent carbonyl function­alities (via Wacker reaction), and cyclopentenone annulation was effected by aldol condensation.",
publisher = "Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Synthetic study on the angular triquinanes: Scientific paper",
volume = "88",
number = "10",
pages = "975-983",
doi = "10.2298/JSC230627046S"
}

Stjepanovic, M., Janković, A., Vulović, B., Matović, R.,& Saičić, R.. (2023). Synthetic study on the angular triquinanes: Scientific paper. in Journal of the Serbian Chemical Society
Serbian Chemical Society., 88(10), 975-983.
https://doi.org/10.2298/JSC230627046S

Stjepanovic M, Janković A, Vulović B, Matović R, Saičić R. Synthetic study on the angular triquinanes: Scientific paper. in Journal of the Serbian Chemical Society. 2023;88(10):975-983.
doi:10.2298/JSC230627046S .

Stjepanovic, Mihailo, Janković, Aleksandar, Vulović, Bojan, Matović, Radomir, Saičić, Radomir, "Synthetic study on the angular triquinanes: Scientific paper" in Journal of the Serbian Chemical Society, 88, no. 10 (2023):975-983,
https://doi.org/10.2298/JSC230627046S . .

TY  - JOUR
AU  - Kokić, Branislav
AU  - Vulović, Bojan
AU  - Jović, Miloš
AU  - Andrijević, Ana
AU  - Ajdačić, Vladimir
AU  - Opsenica, Igor
PY  - 2023
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/6299
AB  - Прегледни чланак о до сад објављеним методама за кобалтом-катализовану адицију угљеничних електрофила на карбонилну и иминску функцију.
AB  - The addition of carbon electrophiles to carbonyls and imines has emerged as a valuable strategy for the construction of C−C bonds. The merger of this concept with sustainable cobalt catalysis has yielded numerous innovative methodologies. Remarkable functional group tolerance and selectivity have been observed in many cases, providing reliable methods for bond construction. The cobalt-catalyzed additions of carbon electrophiles to carbonyls, imines and carboxylic acid derivatives described in this review include the earliest reports, such as Takai-Utimoto Co/Cr co-catalyzed additions and their progression, as well as modern variants, exemplified by recent Co/photoredox co-catalyzed protocols. The systematic appraisal of this modern strategy provides a clearer perspective and inspiration for its further development.
PB  - Wiley
T2  - European Journal of Organic Chemistry
T1  - Strategies for Carbon Electrophile Addition to Carbonyls and Imines by Cobalt Catalysis
VL  - 26
IS  - 45
SP  - e202300997
DO  - 10.1002/ejoc.202300997
ER  - 

@article{
author = "Kokić, Branislav and Vulović, Bojan and Jović, Miloš and Andrijević, Ana and Ajdačić, Vladimir and Opsenica, Igor",
year = "2023",
abstract = "Прегледни чланак о до сад објављеним методама за кобалтом-катализовану адицију угљеничних електрофила на карбонилну и иминску функцију., The addition of carbon electrophiles to carbonyls and imines has emerged as a valuable strategy for the construction of C−C bonds. The merger of this concept with sustainable cobalt catalysis has yielded numerous innovative methodologies. Remarkable functional group tolerance and selectivity have been observed in many cases, providing reliable methods for bond construction. The cobalt-catalyzed additions of carbon electrophiles to carbonyls, imines and carboxylic acid derivatives described in this review include the earliest reports, such as Takai-Utimoto Co/Cr co-catalyzed additions and their progression, as well as modern variants, exemplified by recent Co/photoredox co-catalyzed protocols. The systematic appraisal of this modern strategy provides a clearer perspective and inspiration for its further development.",
publisher = "Wiley",
journal = "European Journal of Organic Chemistry",
title = "Strategies for Carbon Electrophile Addition to Carbonyls and Imines by Cobalt Catalysis",
volume = "26",
number = "45",
pages = "e202300997",
doi = "10.1002/ejoc.202300997"
}

Kokić, B., Vulović, B., Jović, M., Andrijević, A., Ajdačić, V.,& Opsenica, I.. (2023). Strategies for Carbon Electrophile Addition to Carbonyls and Imines by Cobalt Catalysis. in European Journal of Organic Chemistry
Wiley., 26(45), e202300997.
https://doi.org/10.1002/ejoc.202300997

Kokić B, Vulović B, Jović M, Andrijević A, Ajdačić V, Opsenica I. Strategies for Carbon Electrophile Addition to Carbonyls and Imines by Cobalt Catalysis. in European Journal of Organic Chemistry. 2023;26(45):e202300997.
doi:10.1002/ejoc.202300997 .

Kokić, Branislav, Vulović, Bojan, Jović, Miloš, Andrijević, Ana, Ajdačić, Vladimir, Opsenica, Igor, "Strategies for Carbon Electrophile Addition to Carbonyls and Imines by Cobalt Catalysis" in European Journal of Organic Chemistry, 26, no. 45 (2023):e202300997,
https://doi.org/10.1002/ejoc.202300997 . .

TY  - JOUR
AU  - Vulović, Bojan
AU  - Trmčić, Milena
AU  - Matović, Radomir
AU  - Saičić, Radomir
PY  - 2019
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3819
AB  - Unsaturated oxyallyl cations with a suitably positioned alkene bond undergo 5-exo-cyclization with the formation of vinylcyclopentane derivatives. Alkyne analogues provide allenes. The reaction proceeds with a moderate to excellent level of stereoselectivity and allows for asymmetric induction in the reaction with chiral substrate.
PB  - ACS
T2  - Organic Letters
T1  - Cyclization Reactions of Oxyallyl Cation. A Method for Cyclopentane Ring Formation
VL  - 21
IS  - 23
SP  - 9618
EP  - 9621
DO  - 10.1021/acs.orglett.9b03791
ER  - 

@article{
author = "Vulović, Bojan and Trmčić, Milena and Matović, Radomir and Saičić, Radomir",
year = "2019",
abstract = "Unsaturated oxyallyl cations with a suitably positioned alkene bond undergo 5-exo-cyclization with the formation of vinylcyclopentane derivatives. Alkyne analogues provide allenes. The reaction proceeds with a moderate to excellent level of stereoselectivity and allows for asymmetric induction in the reaction with chiral substrate.",
publisher = "ACS",
journal = "Organic Letters",
title = "Cyclization Reactions of Oxyallyl Cation. A Method for Cyclopentane Ring Formation",
volume = "21",
number = "23",
pages = "9618-9621",
doi = "10.1021/acs.orglett.9b03791"
}

Vulović, B., Trmčić, M., Matović, R.,& Saičić, R.. (2019). Cyclization Reactions of Oxyallyl Cation. A Method for Cyclopentane Ring Formation. in Organic Letters
ACS., 21(23), 9618-9621.
https://doi.org/10.1021/acs.orglett.9b03791

Vulović B, Trmčić M, Matović R, Saičić R. Cyclization Reactions of Oxyallyl Cation. A Method for Cyclopentane Ring Formation. in Organic Letters. 2019;21(23):9618-9621.
doi:10.1021/acs.orglett.9b03791 .

Vulović, Bojan, Trmčić, Milena, Matović, Radomir, Saičić, Radomir, "Cyclization Reactions of Oxyallyl Cation. A Method for Cyclopentane Ring Formation" in Organic Letters, 21, no. 23 (2019):9618-9621,
https://doi.org/10.1021/acs.orglett.9b03791 . .

TY  - DATA
AU  - Vulović, Bojan
AU  - Trmčić, Milena
AU  - Matović, Radomir
AU  - Saičić, Radomir
PY  - 2019
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3841
PB  - ACS
T2  - Organic Letters
T1  - Supplementary data for the article: Vulovic, B.; Trmcic, M.; Matovic, R.; Saicic, R. N. Cyclization Reactions of Oxyallyl Cation. A Method for Cyclopentane Ring Formation. Organic Letters 2019, 21 (23), 9618–9621. https://doi.org/10.1021/acs.orglett.9b03791
UR  - https://hdl.handle.net/21.15107/rcub_cherry_3841
ER  - 

@misc{
author = "Vulović, Bojan and Trmčić, Milena and Matović, Radomir and Saičić, Radomir",
year = "2019",
publisher = "ACS",
journal = "Organic Letters",
title = "Supplementary data for the article: Vulovic, B.; Trmcic, M.; Matovic, R.; Saicic, R. N. Cyclization Reactions of Oxyallyl Cation. A Method for Cyclopentane Ring Formation. Organic Letters 2019, 21 (23), 9618–9621. https://doi.org/10.1021/acs.orglett.9b03791",
url = "https://hdl.handle.net/21.15107/rcub_cherry_3841"
}

Vulović, B., Trmčić, M., Matović, R.,& Saičić, R.. (2019). Supplementary data for the article: Vulovic, B.; Trmcic, M.; Matovic, R.; Saicic, R. N. Cyclization Reactions of Oxyallyl Cation. A Method for Cyclopentane Ring Formation. Organic Letters 2019, 21 (23), 9618–9621. https://doi.org/10.1021/acs.orglett.9b03791. in Organic Letters
ACS..
https://hdl.handle.net/21.15107/rcub_cherry_3841

Vulović B, Trmčić M, Matović R, Saičić R. Supplementary data for the article: Vulovic, B.; Trmcic, M.; Matovic, R.; Saicic, R. N. Cyclization Reactions of Oxyallyl Cation. A Method for Cyclopentane Ring Formation. Organic Letters 2019, 21 (23), 9618–9621. https://doi.org/10.1021/acs.orglett.9b03791. in Organic Letters. 2019;.
https://hdl.handle.net/21.15107/rcub_cherry_3841 .

Vulović, Bojan, Trmčić, Milena, Matović, Radomir, Saičić, Radomir, "Supplementary data for the article: Vulovic, B.; Trmcic, M.; Matovic, R.; Saicic, R. N. Cyclization Reactions of Oxyallyl Cation. A Method for Cyclopentane Ring Formation. Organic Letters 2019, 21 (23), 9618–9621. https://doi.org/10.1021/acs.orglett.9b03791" in Organic Letters (2019),
https://hdl.handle.net/21.15107/rcub_cherry_3841 .

TY  - JOUR
AU  - Bihelović, Filip
AU  - Vulović, Bojan
AU  - Saičić, Radomir
PY  - 2018
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2156
AB  - The advent of gold catalysis has transformed hydroxyalkoxylation of alkynes - once a rudimentary, mercury(II)-, or silver(I)-catalyzed process limited to structurally simple substrates - into a sophisticated method that has found application in syntheses of highly complex organic molecules. This transformation can further be combined with carbon-carbon bond-forming reactions into domino sequences that allow for a considerable increase of molecular complexity within a single synthetic step. Some recent examples of the development and synthetic applications of these reactions are provided.
PB  - Wiley-V C H Verlag Gmbh, Weinheim
T2  - Israel Journal of Chemistry
T1  - Gold(I)-Catalyzed C-O/C-C Bond-Forming Domino Reactions and Their Synthetic Applications
VL  - 58
IS  - 5
SP  - 521
EP  - 530
DO  - 10.1002/ijch.201700033
ER  - 

@article{
author = "Bihelović, Filip and Vulović, Bojan and Saičić, Radomir",
year = "2018",
abstract = "The advent of gold catalysis has transformed hydroxyalkoxylation of alkynes - once a rudimentary, mercury(II)-, or silver(I)-catalyzed process limited to structurally simple substrates - into a sophisticated method that has found application in syntheses of highly complex organic molecules. This transformation can further be combined with carbon-carbon bond-forming reactions into domino sequences that allow for a considerable increase of molecular complexity within a single synthetic step. Some recent examples of the development and synthetic applications of these reactions are provided.",
publisher = "Wiley-V C H Verlag Gmbh, Weinheim",
journal = "Israel Journal of Chemistry",
title = "Gold(I)-Catalyzed C-O/C-C Bond-Forming Domino Reactions and Their Synthetic Applications",
volume = "58",
number = "5",
pages = "521-530",
doi = "10.1002/ijch.201700033"
}

Bihelović, F., Vulović, B.,& Saičić, R.. (2018). Gold(I)-Catalyzed C-O/C-C Bond-Forming Domino Reactions and Their Synthetic Applications. in Israel Journal of Chemistry
Wiley-V C H Verlag Gmbh, Weinheim., 58(5), 521-530.
https://doi.org/10.1002/ijch.201700033

Bihelović F, Vulović B, Saičić R. Gold(I)-Catalyzed C-O/C-C Bond-Forming Domino Reactions and Their Synthetic Applications. in Israel Journal of Chemistry. 2018;58(5):521-530.
doi:10.1002/ijch.201700033 .

Bihelović, Filip, Vulović, Bojan, Saičić, Radomir, "Gold(I)-Catalyzed C-O/C-C Bond-Forming Domino Reactions and Their Synthetic Applications" in Israel Journal of Chemistry, 58, no. 5 (2018):521-530,
https://doi.org/10.1002/ijch.201700033 . .

TY  - JOUR
AU  - Bihelović, Filip
AU  - Vulović, Bojan
AU  - Saičić, Radomir
PY  - 2017
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2512
AB  - During our attempt to follow the planned synthetic route to the naturally occurring antibiotic (-)-atrop-abyssomicin C, we encountered two shortcomings, which forced us to reconsider our tactics and find new methods to overcome the problems. These methods turned out to be of general applicability, as demonstrated later in total syntheses of two other natural products: (+)-allokainic acid and (-)-gabosine H. The paper provides a brief account of these endeavors.
PB  - Natural Products Inc, Westerville
T2  - Natural Product Communications
T1  - Synthesis of Natural Products and the Development of Synthetic Methodology: The Case Study of (-)-Atrop-abyssomicin C
VL  - 12
IS  - 8
SP  - 1209
EP  - 1214
UR  - https://hdl.handle.net/21.15107/rcub_cherry_2512
ER  - 

@article{
author = "Bihelović, Filip and Vulović, Bojan and Saičić, Radomir",
year = "2017",
abstract = "During our attempt to follow the planned synthetic route to the naturally occurring antibiotic (-)-atrop-abyssomicin C, we encountered two shortcomings, which forced us to reconsider our tactics and find new methods to overcome the problems. These methods turned out to be of general applicability, as demonstrated later in total syntheses of two other natural products: (+)-allokainic acid and (-)-gabosine H. The paper provides a brief account of these endeavors.",
publisher = "Natural Products Inc, Westerville",
journal = "Natural Product Communications",
title = "Synthesis of Natural Products and the Development of Synthetic Methodology: The Case Study of (-)-Atrop-abyssomicin C",
volume = "12",
number = "8",
pages = "1209-1214",
url = "https://hdl.handle.net/21.15107/rcub_cherry_2512"
}

Bihelović, F., Vulović, B.,& Saičić, R.. (2017). Synthesis of Natural Products and the Development of Synthetic Methodology: The Case Study of (-)-Atrop-abyssomicin C. in Natural Product Communications
Natural Products Inc, Westerville., 12(8), 1209-1214.
https://hdl.handle.net/21.15107/rcub_cherry_2512

Bihelović F, Vulović B, Saičić R. Synthesis of Natural Products and the Development of Synthetic Methodology: The Case Study of (-)-Atrop-abyssomicin C. in Natural Product Communications. 2017;12(8):1209-1214.
https://hdl.handle.net/21.15107/rcub_cherry_2512 .

Bihelović, Filip, Vulović, Bojan, Saičić, Radomir, "Synthesis of Natural Products and the Development of Synthetic Methodology: The Case Study of (-)-Atrop-abyssomicin C" in Natural Product Communications, 12, no. 8 (2017):1209-1214,
https://hdl.handle.net/21.15107/rcub_cherry_2512 .

TY  - JOUR
AU  - Cinderella, Andrew P.
AU  - Vulović, Bojan
AU  - Watson, Donald A.
PY  - 2017
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2475
AB  - We report the first example of a silyl-Negishi reaction between secondary zinc organometallics and silicon electrophiles. This palladium-catalyzed process provides direct access to alkyl silanes. The delicate balance of steric and electronic parameters of the employed DrewPhos ligand is paramount to suppressing isomerization and promoting efficient and selective cross-coupling.
PB  - Amer Chemical Soc, Washington
T2  - Journal of the American Chemical Society
T1  - Palladium-Catalyzed Cross-Coupling of Silyl Electrophiles with Alkylzinc Halides: A Silyl-Negishi Reaction
VL  - 139
IS  - 23
SP  - 7741
EP  - 7744
DO  - 10.1021/jacs.7b04364
ER  - 

@article{
author = "Cinderella, Andrew P. and Vulović, Bojan and Watson, Donald A.",
year = "2017",
abstract = "We report the first example of a silyl-Negishi reaction between secondary zinc organometallics and silicon electrophiles. This palladium-catalyzed process provides direct access to alkyl silanes. The delicate balance of steric and electronic parameters of the employed DrewPhos ligand is paramount to suppressing isomerization and promoting efficient and selective cross-coupling.",
publisher = "Amer Chemical Soc, Washington",
journal = "Journal of the American Chemical Society",
title = "Palladium-Catalyzed Cross-Coupling of Silyl Electrophiles with Alkylzinc Halides: A Silyl-Negishi Reaction",
volume = "139",
number = "23",
pages = "7741-7744",
doi = "10.1021/jacs.7b04364"
}

Cinderella, A. P., Vulović, B.,& Watson, D. A.. (2017). Palladium-Catalyzed Cross-Coupling of Silyl Electrophiles with Alkylzinc Halides: A Silyl-Negishi Reaction. in Journal of the American Chemical Society
Amer Chemical Soc, Washington., 139(23), 7741-7744.
https://doi.org/10.1021/jacs.7b04364

Cinderella AP, Vulović B, Watson DA. Palladium-Catalyzed Cross-Coupling of Silyl Electrophiles with Alkylzinc Halides: A Silyl-Negishi Reaction. in Journal of the American Chemical Society. 2017;139(23):7741-7744.
doi:10.1021/jacs.7b04364 .

Cinderella, Andrew P., Vulović, Bojan, Watson, Donald A., "Palladium-Catalyzed Cross-Coupling of Silyl Electrophiles with Alkylzinc Halides: A Silyl-Negishi Reaction" in Journal of the American Chemical Society, 139, no. 23 (2017):7741-7744,
https://doi.org/10.1021/jacs.7b04364 . .

TY  - JOUR
AU  - Vulović, Bojan
AU  - Watson, Donald A.
PY  - 2017
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2525
AB  - Since the discovery of the Heck reaction in the early seventies, the reaction has become a powerful tool in synthetic organic chemistry. By employing heteroatomic instead of traditional carbon electrophiles, the Heck reaction shows an intriguing flexibility. These hetereoatomic Heck reactions reinvigorate the area, by offering new routes to highly useful synthetic precursors and structural motifs present in biologically active compounds. This microreview focuses on early developments leading to the heteroatomic-Heck reactions (silyl-Heck, boryl-Heck and intramolecular aza-Heck), current state of the emerging area, as well as that of a few related processes.
PB  - Wiley-V C H Verlag Gmbh, Weinheim
T2  - European Journal of Organic Chemistry
T1  - Heck-Like Reactions Involving Heteroatomic Electrophiles
IS  - 34
SP  - 4996
EP  - 5009
DO  - 10.1002/ejoc.201700485
ER  - 

@article{
author = "Vulović, Bojan and Watson, Donald A.",
year = "2017",
abstract = "Since the discovery of the Heck reaction in the early seventies, the reaction has become a powerful tool in synthetic organic chemistry. By employing heteroatomic instead of traditional carbon electrophiles, the Heck reaction shows an intriguing flexibility. These hetereoatomic Heck reactions reinvigorate the area, by offering new routes to highly useful synthetic precursors and structural motifs present in biologically active compounds. This microreview focuses on early developments leading to the heteroatomic-Heck reactions (silyl-Heck, boryl-Heck and intramolecular aza-Heck), current state of the emerging area, as well as that of a few related processes.",
publisher = "Wiley-V C H Verlag Gmbh, Weinheim",
journal = "European Journal of Organic Chemistry",
title = "Heck-Like Reactions Involving Heteroatomic Electrophiles",
number = "34",
pages = "4996-5009",
doi = "10.1002/ejoc.201700485"
}

Vulović, B.,& Watson, D. A.. (2017). Heck-Like Reactions Involving Heteroatomic Electrophiles. in European Journal of Organic Chemistry
Wiley-V C H Verlag Gmbh, Weinheim.(34), 4996-5009.
https://doi.org/10.1002/ejoc.201700485

Vulović B, Watson DA. Heck-Like Reactions Involving Heteroatomic Electrophiles. in European Journal of Organic Chemistry. 2017;(34):4996-5009.
doi:10.1002/ejoc.201700485 .

Vulović, Bojan, Watson, Donald A., "Heck-Like Reactions Involving Heteroatomic Electrophiles" in European Journal of Organic Chemistry, no. 34 (2017):4996-5009,
https://doi.org/10.1002/ejoc.201700485 . .

TY  - DATA
AU  - Cinderella, Andrew P.
AU  - Vulović, Bojan
AU  - Watson, Donald A.
PY  - 2017
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3099
PB  - Amer Chemical Soc, Washington
T2  - Journal of the American Chemical Society
T1  - Supplementary data for article:           Cinderella, A. P.; Vulovic, B.; Watson, D. A. Palladium-Catalyzed Cross-Coupling of Silyl Electrophiles with Alkylzinc Halides: A Silyl-Negishi Reaction. Journal of the American Chemical Society 2017, 139 (23), 7741–7744. https://doi.org/10.1021/jacs.7b04364
UR  - https://hdl.handle.net/21.15107/rcub_cherry_3099
ER  - 

@misc{
author = "Cinderella, Andrew P. and Vulović, Bojan and Watson, Donald A.",
year = "2017",
publisher = "Amer Chemical Soc, Washington",
journal = "Journal of the American Chemical Society",
title = "Supplementary data for article:           Cinderella, A. P.; Vulovic, B.; Watson, D. A. Palladium-Catalyzed Cross-Coupling of Silyl Electrophiles with Alkylzinc Halides: A Silyl-Negishi Reaction. Journal of the American Chemical Society 2017, 139 (23), 7741–7744. https://doi.org/10.1021/jacs.7b04364",
url = "https://hdl.handle.net/21.15107/rcub_cherry_3099"
}

Cinderella, A. P., Vulović, B.,& Watson, D. A.. (2017). Supplementary data for article:           Cinderella, A. P.; Vulovic, B.; Watson, D. A. Palladium-Catalyzed Cross-Coupling of Silyl Electrophiles with Alkylzinc Halides: A Silyl-Negishi Reaction. Journal of the American Chemical Society 2017, 139 (23), 7741–7744. https://doi.org/10.1021/jacs.7b04364. in Journal of the American Chemical Society
Amer Chemical Soc, Washington..
https://hdl.handle.net/21.15107/rcub_cherry_3099

Cinderella AP, Vulović B, Watson DA. Supplementary data for article:           Cinderella, A. P.; Vulovic, B.; Watson, D. A. Palladium-Catalyzed Cross-Coupling of Silyl Electrophiles with Alkylzinc Halides: A Silyl-Negishi Reaction. Journal of the American Chemical Society 2017, 139 (23), 7741–7744. https://doi.org/10.1021/jacs.7b04364. in Journal of the American Chemical Society. 2017;.
https://hdl.handle.net/21.15107/rcub_cherry_3099 .

Cinderella, Andrew P., Vulović, Bojan, Watson, Donald A., "Supplementary data for article:           Cinderella, A. P.; Vulovic, B.; Watson, D. A. Palladium-Catalyzed Cross-Coupling of Silyl Electrophiles with Alkylzinc Halides: A Silyl-Negishi Reaction. Journal of the American Chemical Society 2017, 139 (23), 7741–7744. https://doi.org/10.1021/jacs.7b04364" in Journal of the American Chemical Society (2017),
https://hdl.handle.net/21.15107/rcub_cherry_3099 .

TY  - JOUR
AU  - Vulović, Bojan
AU  - Cinderella, Andrew P.
AU  - Watson, Donald A.
PY  - 2017
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3923
AB  - Using a palladium catalyst supported by DrewPhos, the alkylation of monochlorosilanes with primary and secondary alkylmagnesium halides is now possible. Arylation with sterically demanding aromatic magnesium halides is also enabled. This transformation overcomes the high bond strength of the Si–Cl bond (113 kcal/mol) and is a rare example of a transition-metal catalyzed process involving its activation. Because of the availability of both chlorosilanes and organomagnesium halide reagents, this method allows for the preparation of a wide range of alkyl and aryl silanes.
PB  - American Chemical Society
T2  - ACS Catalysis
T1  - Palladium-Catalyzed Cross-Coupling of Monochlorosilanes and Grignard Reagents
VL  - 7
IS  - 12
SP  - 8113
EP  - 8117
DO  - 10.1021/acscatal.7b03465
ER  - 

@article{
author = "Vulović, Bojan and Cinderella, Andrew P. and Watson, Donald A.",
year = "2017",
abstract = "Using a palladium catalyst supported by DrewPhos, the alkylation of monochlorosilanes with primary and secondary alkylmagnesium halides is now possible. Arylation with sterically demanding aromatic magnesium halides is also enabled. This transformation overcomes the high bond strength of the Si–Cl bond (113 kcal/mol) and is a rare example of a transition-metal catalyzed process involving its activation. Because of the availability of both chlorosilanes and organomagnesium halide reagents, this method allows for the preparation of a wide range of alkyl and aryl silanes.",
publisher = "American Chemical Society",
journal = "ACS Catalysis",
title = "Palladium-Catalyzed Cross-Coupling of Monochlorosilanes and Grignard Reagents",
volume = "7",
number = "12",
pages = "8113-8117",
doi = "10.1021/acscatal.7b03465"
}

Vulović, B., Cinderella, A. P.,& Watson, D. A.. (2017). Palladium-Catalyzed Cross-Coupling of Monochlorosilanes and Grignard Reagents. in ACS Catalysis
American Chemical Society., 7(12), 8113-8117.
https://doi.org/10.1021/acscatal.7b03465

Vulović B, Cinderella AP, Watson DA. Palladium-Catalyzed Cross-Coupling of Monochlorosilanes and Grignard Reagents. in ACS Catalysis. 2017;7(12):8113-8117.
doi:10.1021/acscatal.7b03465 .

Vulović, Bojan, Cinderella, Andrew P., Watson, Donald A., "Palladium-Catalyzed Cross-Coupling of Monochlorosilanes and Grignard Reagents" in ACS Catalysis, 7, no. 12 (2017):8113-8117,
https://doi.org/10.1021/acscatal.7b03465 . .

TY  - DATA
AU  - Vulović, Bojan
AU  - Cinderella, Andrew P.
AU  - Watson, Donald A.
PY  - 2017
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3924
PB  - American Chemical Society
T2  - ACS Catalysis
T1  - Supplementary data for the article: Vulović, B.; Cinderella, A. P.; Watson, D. A. Palladium-Catalyzed Cross-Coupling of Monochlorosilanes and Grignard Reagents. ACS Catalysis 2017, 7 (12), 8113–8117. https://doi.org/10.1021/acscatal.7b03465
UR  - https://hdl.handle.net/21.15107/rcub_cherry_3924
ER  - 

@misc{
author = "Vulović, Bojan and Cinderella, Andrew P. and Watson, Donald A.",
year = "2017",
publisher = "American Chemical Society",
journal = "ACS Catalysis",
title = "Supplementary data for the article: Vulović, B.; Cinderella, A. P.; Watson, D. A. Palladium-Catalyzed Cross-Coupling of Monochlorosilanes and Grignard Reagents. ACS Catalysis 2017, 7 (12), 8113–8117. https://doi.org/10.1021/acscatal.7b03465",
url = "https://hdl.handle.net/21.15107/rcub_cherry_3924"
}

Vulović, B., Cinderella, A. P.,& Watson, D. A.. (2017). Supplementary data for the article: Vulović, B.; Cinderella, A. P.; Watson, D. A. Palladium-Catalyzed Cross-Coupling of Monochlorosilanes and Grignard Reagents. ACS Catalysis 2017, 7 (12), 8113–8117. https://doi.org/10.1021/acscatal.7b03465. in ACS Catalysis
American Chemical Society..
https://hdl.handle.net/21.15107/rcub_cherry_3924

Vulović B, Cinderella AP, Watson DA. Supplementary data for the article: Vulović, B.; Cinderella, A. P.; Watson, D. A. Palladium-Catalyzed Cross-Coupling of Monochlorosilanes and Grignard Reagents. ACS Catalysis 2017, 7 (12), 8113–8117. https://doi.org/10.1021/acscatal.7b03465. in ACS Catalysis. 2017;.
https://hdl.handle.net/21.15107/rcub_cherry_3924 .

Vulović, Bojan, Cinderella, Andrew P., Watson, Donald A., "Supplementary data for the article: Vulović, B.; Cinderella, A. P.; Watson, D. A. Palladium-Catalyzed Cross-Coupling of Monochlorosilanes and Grignard Reagents. ACS Catalysis 2017, 7 (12), 8113–8117. https://doi.org/10.1021/acscatal.7b03465" in ACS Catalysis (2017),
https://hdl.handle.net/21.15107/rcub_cherry_3924 .

TY  - JOUR
AU  - Vulović, Bojan
AU  - Cinderella, Andrew P.
AU  - Watson, Donald A.
PY  - 2017
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3925
AB  - Using a palladium catalyst supported by DrewPhos, the alkylation of monochlorosilanes with primary and secondary alkylmagnesium halides is now possible. Arylation with sterically demanding aromatic magnesium halides is also enabled. This transformation overcomes the high bond strength of the Si–Cl bond (113 kcal/mol) and is a rare example of a transition-metal catalyzed process involving its activation. Because of the availability of both chlorosilanes and organomagnesium halide reagents, this method allows for the preparation of a wide range of alkyl and aryl silanes.
PB  - American Chemical Society
T2  - ACS Catalysis
T1  - Palladium-Catalyzed Cross-Coupling of Monochlorosilanes and Grignard Reagents
VL  - 7
IS  - 12
SP  - 8113
EP  - 8117
DO  - 10.1021/acscatal.7b03465
ER  - 

@article{
author = "Vulović, Bojan and Cinderella, Andrew P. and Watson, Donald A.",
year = "2017",
abstract = "Using a palladium catalyst supported by DrewPhos, the alkylation of monochlorosilanes with primary and secondary alkylmagnesium halides is now possible. Arylation with sterically demanding aromatic magnesium halides is also enabled. This transformation overcomes the high bond strength of the Si–Cl bond (113 kcal/mol) and is a rare example of a transition-metal catalyzed process involving its activation. Because of the availability of both chlorosilanes and organomagnesium halide reagents, this method allows for the preparation of a wide range of alkyl and aryl silanes.",
publisher = "American Chemical Society",
journal = "ACS Catalysis",
title = "Palladium-Catalyzed Cross-Coupling of Monochlorosilanes and Grignard Reagents",
volume = "7",
number = "12",
pages = "8113-8117",
doi = "10.1021/acscatal.7b03465"
}

Vulović, B., Cinderella, A. P.,& Watson, D. A.. (2017). Palladium-Catalyzed Cross-Coupling of Monochlorosilanes and Grignard Reagents. in ACS Catalysis
American Chemical Society., 7(12), 8113-8117.
https://doi.org/10.1021/acscatal.7b03465

Vulović B, Cinderella AP, Watson DA. Palladium-Catalyzed Cross-Coupling of Monochlorosilanes and Grignard Reagents. in ACS Catalysis. 2017;7(12):8113-8117.
doi:10.1021/acscatal.7b03465 .

Vulović, Bojan, Cinderella, Andrew P., Watson, Donald A., "Palladium-Catalyzed Cross-Coupling of Monochlorosilanes and Grignard Reagents" in ACS Catalysis, 7, no. 12 (2017):8113-8117,
https://doi.org/10.1021/acscatal.7b03465 . .

TY  - JOUR
AU  - Vulović, Bojan
AU  - Kolarski, Dušan
AU  - Bihelović, Filip
AU  - Matović, Radomir
AU  - Gruden-Pavlović, Maja
AU  - Saičić, Radomir
PY  - 2016
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2290
AB  - 1,6-Diynes with a t-butylcarbonate group in the propargylic position undergo gold(I)-catalyzed dominocyclization which affords alpha-hydroxycyclohexenones. The described sequence can be applied on functionalized, highly oxygenated substrates, as examplified in the synthesis of (-)-gabosine H and its epimer.
PB  - Amer Chemical Soc, Washington
T2  - Organic Letters
T1  - Gold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (-)-Gabosine H and (-)-6-epi-Gabosine H
VL  - 18
IS  - 15
SP  - 3886
EP  - 3889
DO  - 10.1021/acs.orglett.6b01898
ER  - 

@article{
author = "Vulović, Bojan and Kolarski, Dušan and Bihelović, Filip and Matović, Radomir and Gruden-Pavlović, Maja and Saičić, Radomir",
year = "2016",
abstract = "1,6-Diynes with a t-butylcarbonate group in the propargylic position undergo gold(I)-catalyzed dominocyclization which affords alpha-hydroxycyclohexenones. The described sequence can be applied on functionalized, highly oxygenated substrates, as examplified in the synthesis of (-)-gabosine H and its epimer.",
publisher = "Amer Chemical Soc, Washington",
journal = "Organic Letters",
title = "Gold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (-)-Gabosine H and (-)-6-epi-Gabosine H",
volume = "18",
number = "15",
pages = "3886-3889",
doi = "10.1021/acs.orglett.6b01898"
}

Vulović, B., Kolarski, D., Bihelović, F., Matović, R., Gruden-Pavlović, M.,& Saičić, R.. (2016). Gold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (-)-Gabosine H and (-)-6-epi-Gabosine H. in Organic Letters
Amer Chemical Soc, Washington., 18(15), 3886-3889.
https://doi.org/10.1021/acs.orglett.6b01898

Vulović B, Kolarski D, Bihelović F, Matović R, Gruden-Pavlović M, Saičić R. Gold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (-)-Gabosine H and (-)-6-epi-Gabosine H. in Organic Letters. 2016;18(15):3886-3889.
doi:10.1021/acs.orglett.6b01898 .

Vulović, Bojan, Kolarski, Dušan, Bihelović, Filip, Matović, Radomir, Gruden-Pavlović, Maja, Saičić, Radomir, "Gold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (-)-Gabosine H and (-)-6-epi-Gabosine H" in Organic Letters, 18, no. 15 (2016):3886-3889,
https://doi.org/10.1021/acs.orglett.6b01898 . .

TY  - JOUR
AU  - Vulović, Bojan
AU  - Kolarski, Dušan
AU  - Bihelović, Filip
AU  - Matović, Radomir
AU  - Gruden-Pavlović, Maja
AU  - Saičić, Radomir
PY  - 2016
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2327
PB  - Amer Chemical Soc, Washington
T2  - Organic Letters
T1  - Gold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (-)-Gabosine H and (-)-6-epi-Gabosine H (vol 18, pg 3886, 2016)
VL  - 18
IS  - 19
SP  - 5186
EP  - 5187
DO  - 10.1021/acs.orglett.6b02509
ER  - 

@article{
author = "Vulović, Bojan and Kolarski, Dušan and Bihelović, Filip and Matović, Radomir and Gruden-Pavlović, Maja and Saičić, Radomir",
year = "2016",
publisher = "Amer Chemical Soc, Washington",
journal = "Organic Letters",
title = "Gold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (-)-Gabosine H and (-)-6-epi-Gabosine H (vol 18, pg 3886, 2016)",
volume = "18",
number = "19",
pages = "5186-5187",
doi = "10.1021/acs.orglett.6b02509"
}

Vulović, B., Kolarski, D., Bihelović, F., Matović, R., Gruden-Pavlović, M.,& Saičić, R.. (2016). Gold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (-)-Gabosine H and (-)-6-epi-Gabosine H (vol 18, pg 3886, 2016). in Organic Letters
Amer Chemical Soc, Washington., 18(19), 5186-5187.
https://doi.org/10.1021/acs.orglett.6b02509

Vulović B, Kolarski D, Bihelović F, Matović R, Gruden-Pavlović M, Saičić R. Gold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (-)-Gabosine H and (-)-6-epi-Gabosine H (vol 18, pg 3886, 2016). in Organic Letters. 2016;18(19):5186-5187.
doi:10.1021/acs.orglett.6b02509 .

Vulović, Bojan, Kolarski, Dušan, Bihelović, Filip, Matović, Radomir, Gruden-Pavlović, Maja, Saičić, Radomir, "Gold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (-)-Gabosine H and (-)-6-epi-Gabosine H (vol 18, pg 3886, 2016)" in Organic Letters, 18, no. 19 (2016):5186-5187,
https://doi.org/10.1021/acs.orglett.6b02509 . .

TY  - DATA
AU  - Vulović, Bojan
AU  - Kolarski, Dušan
AU  - Bihelović, Filip
AU  - Matović, Radomir
AU  - Gruden-Pavlović, Maja
AU  - Saičić, Radomir
PY  - 2016
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3520
PB  - Amer Chemical Soc, Washington
T2  - Organic Letters
T1  - Supplementary data for the article: Vulovic, B.; Kolarski, D.; Bihelovic, F.; Matovic, R.; Gruden, M.; Saicic, R. N. Gold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (-)-Gabosine H and (-)-6-Epi-Gabosine H. Organic Letters 2016, 18 (15), 3886–3889. https://doi.org/10.1021/acs.orglett.6b01898
UR  - https://hdl.handle.net/21.15107/rcub_cherry_3520
ER  - 

@misc{
author = "Vulović, Bojan and Kolarski, Dušan and Bihelović, Filip and Matović, Radomir and Gruden-Pavlović, Maja and Saičić, Radomir",
year = "2016",
publisher = "Amer Chemical Soc, Washington",
journal = "Organic Letters",
title = "Supplementary data for the article: Vulovic, B.; Kolarski, D.; Bihelovic, F.; Matovic, R.; Gruden, M.; Saicic, R. N. Gold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (-)-Gabosine H and (-)-6-Epi-Gabosine H. Organic Letters 2016, 18 (15), 3886–3889. https://doi.org/10.1021/acs.orglett.6b01898",
url = "https://hdl.handle.net/21.15107/rcub_cherry_3520"
}

Vulović, B., Kolarski, D., Bihelović, F., Matović, R., Gruden-Pavlović, M.,& Saičić, R.. (2016). Supplementary data for the article: Vulovic, B.; Kolarski, D.; Bihelovic, F.; Matovic, R.; Gruden, M.; Saicic, R. N. Gold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (-)-Gabosine H and (-)-6-Epi-Gabosine H. Organic Letters 2016, 18 (15), 3886–3889. https://doi.org/10.1021/acs.orglett.6b01898. in Organic Letters
Amer Chemical Soc, Washington..
https://hdl.handle.net/21.15107/rcub_cherry_3520

Vulović B, Kolarski D, Bihelović F, Matović R, Gruden-Pavlović M, Saičić R. Supplementary data for the article: Vulovic, B.; Kolarski, D.; Bihelovic, F.; Matovic, R.; Gruden, M.; Saicic, R. N. Gold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (-)-Gabosine H and (-)-6-Epi-Gabosine H. Organic Letters 2016, 18 (15), 3886–3889. https://doi.org/10.1021/acs.orglett.6b01898. in Organic Letters. 2016;.
https://hdl.handle.net/21.15107/rcub_cherry_3520 .

Vulović, Bojan, Kolarski, Dušan, Bihelović, Filip, Matović, Radomir, Gruden-Pavlović, Maja, Saičić, Radomir, "Supplementary data for the article: Vulovic, B.; Kolarski, D.; Bihelovic, F.; Matovic, R.; Gruden, M.; Saicic, R. N. Gold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (-)-Gabosine H and (-)-6-Epi-Gabosine H. Organic Letters 2016, 18 (15), 3886–3889. https://doi.org/10.1021/acs.orglett.6b01898" in Organic Letters (2016),
https://hdl.handle.net/21.15107/rcub_cherry_3520 .

TY  - DATA
AU  - Vulović, Bojan
AU  - Marić, Ivana
AU  - Matović, Radomir
AU  - Saičić, Radomir
PY  - 2016
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3629
PB  - Serbian Chemical Soc, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Supplementary data for the article: Vulović, B.; Marić, I.; Matović, R.; Saicíć, R. N. Synthesis of Vinyldihydropyran by Cooperative Catalysis. Journal of the Serbian Chemical Society 2016, 81 (12), 1335–1343. https://doi.org/10.2298/JSC161102103V
UR  - https://hdl.handle.net/21.15107/rcub_cherry_3629
ER  - 

@misc{
author = "Vulović, Bojan and Marić, Ivana and Matović, Radomir and Saičić, Radomir",
year = "2016",
publisher = "Serbian Chemical Soc, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Supplementary data for the article: Vulović, B.; Marić, I.; Matović, R.; Saicíć, R. N. Synthesis of Vinyldihydropyran by Cooperative Catalysis. Journal of the Serbian Chemical Society 2016, 81 (12), 1335–1343. https://doi.org/10.2298/JSC161102103V",
url = "https://hdl.handle.net/21.15107/rcub_cherry_3629"
}

Vulović, B., Marić, I., Matović, R.,& Saičić, R.. (2016). Supplementary data for the article: Vulović, B.; Marić, I.; Matović, R.; Saicíć, R. N. Synthesis of Vinyldihydropyran by Cooperative Catalysis. Journal of the Serbian Chemical Society 2016, 81 (12), 1335–1343. https://doi.org/10.2298/JSC161102103V. in Journal of the Serbian Chemical Society
Serbian Chemical Soc, Belgrade..
https://hdl.handle.net/21.15107/rcub_cherry_3629

Vulović B, Marić I, Matović R, Saičić R. Supplementary data for the article: Vulović, B.; Marić, I.; Matović, R.; Saicíć, R. N. Synthesis of Vinyldihydropyran by Cooperative Catalysis. Journal of the Serbian Chemical Society 2016, 81 (12), 1335–1343. https://doi.org/10.2298/JSC161102103V. in Journal of the Serbian Chemical Society. 2016;.
https://hdl.handle.net/21.15107/rcub_cherry_3629 .

Vulović, Bojan, Marić, Ivana, Matović, Radomir, Saičić, Radomir, "Supplementary data for the article: Vulović, B.; Marić, I.; Matović, R.; Saicíć, R. N. Synthesis of Vinyldihydropyran by Cooperative Catalysis. Journal of the Serbian Chemical Society 2016, 81 (12), 1335–1343. https://doi.org/10.2298/JSC161102103V" in Journal of the Serbian Chemical Society (2016),
https://hdl.handle.net/21.15107/rcub_cherry_3629 .

TY  - JOUR
AU  - Vulović, Bojan
AU  - Marić, Ivana
AU  - Matović, Radomir
AU  - Saičić, Radomir
PY  - 2016
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2388
AB  - Delta(5)-Unsaturated aldehydes with a suitably positioned allylic halide, or phosphate, leaving group undergo doubly-catalyzed cyclization to give dihydropyran derivatives. The cyclization proceeds under the synergetic action of diazabicycloundecene and Pd(PPh3)(4). This type of transformation was also accomplished with an aryl ketone.
PB  - Serbian Chemical Soc, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Synthesis of vinyldihydropyran by cooperative catalysis
VL  - 81
IS  - 12
SP  - 1335
EP  - 1343
DO  - 10.2298/JSC161102103V
ER  - 

@article{
author = "Vulović, Bojan and Marić, Ivana and Matović, Radomir and Saičić, Radomir",
year = "2016",
abstract = "Delta(5)-Unsaturated aldehydes with a suitably positioned allylic halide, or phosphate, leaving group undergo doubly-catalyzed cyclization to give dihydropyran derivatives. The cyclization proceeds under the synergetic action of diazabicycloundecene and Pd(PPh3)(4). This type of transformation was also accomplished with an aryl ketone.",
publisher = "Serbian Chemical Soc, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Synthesis of vinyldihydropyran by cooperative catalysis",
volume = "81",
number = "12",
pages = "1335-1343",
doi = "10.2298/JSC161102103V"
}

Vulović, B., Marić, I., Matović, R.,& Saičić, R.. (2016). Synthesis of vinyldihydropyran by cooperative catalysis. in Journal of the Serbian Chemical Society
Serbian Chemical Soc, Belgrade., 81(12), 1335-1343.
https://doi.org/10.2298/JSC161102103V

Vulović B, Marić I, Matović R, Saičić R. Synthesis of vinyldihydropyran by cooperative catalysis. in Journal of the Serbian Chemical Society. 2016;81(12):1335-1343.
doi:10.2298/JSC161102103V .

Vulović, Bojan, Marić, Ivana, Matović, Radomir, Saičić, Radomir, "Synthesis of vinyldihydropyran by cooperative catalysis" in Journal of the Serbian Chemical Society, 81, no. 12 (2016):1335-1343,
https://doi.org/10.2298/JSC161102103V . .

TY  - THES
AU  - Vulović, Bojan
PY  - 2014
UR  - http://eteze.bg.ac.rs/application/showtheses?thesesId=3263
UR  - https://fedorabg.bg.ac.rs/fedora/get/o:11666/bdef:Content/download
UR  - http://vbs.rs/scripts/cobiss?command=DISPLAY&base=70036&RID=47669775
UR  - http://nardus.mpn.gov.rs/123456789/5904
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2689
AB  - Razvijen je nov pristup sintezi petočlanih i šestočlanih prstenova, zasnovan na
kombinaciji organokatalize i katalize kompleksima prelaznih metala.
Organokatalizovana Tsuji-Trost-ova reakcija omogućuje 5-egzo- i 6-egzo-ciklizacije
aldehida koji u pogodnom položaju poseduju alilnu funkcionalnu grupu, uz nastajanje
karbocikličnih i N-heterocikličnih prstenova. Moguća je i katalitička asimetrična varijanta
reakcije, kojom se dobijaju vinilciklopentanski derivati optičke čistoće više od 98% ee.
Nova reakcija je upotrebljena kao ključni korak u totalnoj sintezi prirodnog proizvoda
(+)-alokainske kiseline i njenog strukturnog analoga. Ciklizacije aldehida koji poseduju
stereocentar odigravaju se stereoselektivno i kontrolisane su supstratom, a stereohemijski
ishod ciklizacija može se predvideti računarskim metodama.
PB  - Универзитет у Београду, Хемијски факултет
T2  - Универзитет у Београду
T1  - Kooperativna kataliza: kombinacija organokatalize i katalize kompleksima prelaznih metala i njena primena u totalnoj sintezi alokainata
T1  - Synergistic catalysis: combination of organocatalysis and organotransition-meta catalysis and application in total synthesis of allokainates.
UR  - https://hdl.handle.net/21.15107/rcub_nardus_5904
ER  - 

@phdthesis{
author = "Vulović, Bojan",
year = "2014",
abstract = "Razvijen je nov pristup sintezi petočlanih i šestočlanih prstenova, zasnovan na
kombinaciji organokatalize i katalize kompleksima prelaznih metala.
Organokatalizovana Tsuji-Trost-ova reakcija omogućuje 5-egzo- i 6-egzo-ciklizacije
aldehida koji u pogodnom položaju poseduju alilnu funkcionalnu grupu, uz nastajanje
karbocikličnih i N-heterocikličnih prstenova. Moguća je i katalitička asimetrična varijanta
reakcije, kojom se dobijaju vinilciklopentanski derivati optičke čistoće više od 98% ee.
Nova reakcija je upotrebljena kao ključni korak u totalnoj sintezi prirodnog proizvoda
(+)-alokainske kiseline i njenog strukturnog analoga. Ciklizacije aldehida koji poseduju
stereocentar odigravaju se stereoselektivno i kontrolisane su supstratom, a stereohemijski
ishod ciklizacija može se predvideti računarskim metodama.",
publisher = "Универзитет у Београду, Хемијски факултет",
journal = "Универзитет у Београду",
title = "Kooperativna kataliza: kombinacija organokatalize i katalize kompleksima prelaznih metala i njena primena u totalnoj sintezi alokainata, Synergistic catalysis: combination of organocatalysis and organotransition-meta catalysis and application in total synthesis of allokainates.",
url = "https://hdl.handle.net/21.15107/rcub_nardus_5904"
}

Vulović, B.. (2014). Kooperativna kataliza: kombinacija organokatalize i katalize kompleksima prelaznih metala i njena primena u totalnoj sintezi alokainata. in Универзитет у Београду
Универзитет у Београду, Хемијски факултет..
https://hdl.handle.net/21.15107/rcub_nardus_5904

Vulović B. Kooperativna kataliza: kombinacija organokatalize i katalize kompleksima prelaznih metala i njena primena u totalnoj sintezi alokainata. in Универзитет у Београду. 2014;.
https://hdl.handle.net/21.15107/rcub_nardus_5904 .

Vulović, Bojan, "Kooperativna kataliza: kombinacija organokatalize i katalize kompleksima prelaznih metala i njena primena u totalnoj sintezi alokainata" in Универзитет у Београду (2014),
https://hdl.handle.net/21.15107/rcub_nardus_5904 .

TY  - THES
AU  - Vulović, Bojan
PY  - 2014
UR  - http://eteze.bg.ac.rs/application/showtheses?thesesId=3263
UR  - https://fedorabg.bg.ac.rs/fedora/get/o:11666/bdef:Content/download
UR  - http://vbs.rs/scripts/cobiss?command=DISPLAY&base=70036&RID=47669775
UR  - http://nardus.mpn.gov.rs/123456789/5904
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2690
AB  - Razvijen je nov pristup sintezi petočlanih i šestočlanih prstenova, zasnovan na
kombinaciji organokatalize i katalize kompleksima prelaznih metala.
Organokatalizovana Tsuji-Trost-ova reakcija omogućuje 5-egzo- i 6-egzo-ciklizacije
aldehida koji u pogodnom položaju poseduju alilnu funkcionalnu grupu, uz nastajanje
karbocikličnih i N-heterocikličnih prstenova. Moguća je i katalitička asimetrična varijanta
reakcije, kojom se dobijaju vinilciklopentanski derivati optičke čistoće više od 98% ee.
Nova reakcija je upotrebljena kao ključni korak u totalnoj sintezi prirodnog proizvoda
(+)-alokainske kiseline i njenog strukturnog analoga. Ciklizacije aldehida koji poseduju
stereocentar odigravaju se stereoselektivno i kontrolisane su supstratom, a stereohemijski
ishod ciklizacija može se predvideti računarskim metodama.
PB  - Универзитет у Београду, Хемијски факултет
T2  - Универзитет у Београду
T1  - Kooperativna kataliza: kombinacija organokatalize i katalize kompleksima prelaznih metala i njena primena u totalnoj sintezi alokainata
T1  - Synergistic catalysis: combination of organocatalysis and organotransition-meta catalysis and application in total synthesis of allokainates.
UR  - https://hdl.handle.net/21.15107/rcub_nardus_5904
ER  - 

@phdthesis{
author = "Vulović, Bojan",
year = "2014",
abstract = "Razvijen je nov pristup sintezi petočlanih i šestočlanih prstenova, zasnovan na
kombinaciji organokatalize i katalize kompleksima prelaznih metala.
Organokatalizovana Tsuji-Trost-ova reakcija omogućuje 5-egzo- i 6-egzo-ciklizacije
aldehida koji u pogodnom položaju poseduju alilnu funkcionalnu grupu, uz nastajanje
karbocikličnih i N-heterocikličnih prstenova. Moguća je i katalitička asimetrična varijanta
reakcije, kojom se dobijaju vinilciklopentanski derivati optičke čistoće više od 98% ee.
Nova reakcija je upotrebljena kao ključni korak u totalnoj sintezi prirodnog proizvoda
(+)-alokainske kiseline i njenog strukturnog analoga. Ciklizacije aldehida koji poseduju
stereocentar odigravaju se stereoselektivno i kontrolisane su supstratom, a stereohemijski
ishod ciklizacija može se predvideti računarskim metodama.",
publisher = "Универзитет у Београду, Хемијски факултет",
journal = "Универзитет у Београду",
title = "Kooperativna kataliza: kombinacija organokatalize i katalize kompleksima prelaznih metala i njena primena u totalnoj sintezi alokainata, Synergistic catalysis: combination of organocatalysis and organotransition-meta catalysis and application in total synthesis of allokainates.",
url = "https://hdl.handle.net/21.15107/rcub_nardus_5904"
}

Vulović, B.. (2014). Kooperativna kataliza: kombinacija organokatalize i katalize kompleksima prelaznih metala i njena primena u totalnoj sintezi alokainata. in Универзитет у Београду
Универзитет у Београду, Хемијски факултет..
https://hdl.handle.net/21.15107/rcub_nardus_5904

Vulović B. Kooperativna kataliza: kombinacija organokatalize i katalize kompleksima prelaznih metala i njena primena u totalnoj sintezi alokainata. in Универзитет у Београду. 2014;.
https://hdl.handle.net/21.15107/rcub_nardus_5904 .

Vulović, Bojan, "Kooperativna kataliza: kombinacija organokatalize i katalize kompleksima prelaznih metala i njena primena u totalnoj sintezi alokainata" in Универзитет у Београду (2014),
https://hdl.handle.net/21.15107/rcub_nardus_5904 .

TY  - JOUR
AU  - Vulović, Bojan
AU  - Gruden-Pavlović, Maja
AU  - Matović, Radomir
AU  - Saičić, Radomir
PY  - 2014
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1475
AB  - Organocatalyzed Tsuji-Trost cyclization of 3b proceeds with asymmetric induction and allows for stereoselective synthesis of (+)-allokainic acid. The stereochemical outcome of the cyclization was predicted by calculations.
PB  - Amer Chemical Soc, Washington
T2  - Organic Letters
T1  - Substrate Stereocontrol in the Intramolecular Organocatalyzed Tsuji-Trost Reaction: Enantioselective Synthesis of Allokainates
VL  - 16
IS  - 1
SP  - 34
EP  - 37
DO  - 10.1021/ol4028557
ER  - 

@article{
author = "Vulović, Bojan and Gruden-Pavlović, Maja and Matović, Radomir and Saičić, Radomir",
year = "2014",
abstract = "Organocatalyzed Tsuji-Trost cyclization of 3b proceeds with asymmetric induction and allows for stereoselective synthesis of (+)-allokainic acid. The stereochemical outcome of the cyclization was predicted by calculations.",
publisher = "Amer Chemical Soc, Washington",
journal = "Organic Letters",
title = "Substrate Stereocontrol in the Intramolecular Organocatalyzed Tsuji-Trost Reaction: Enantioselective Synthesis of Allokainates",
volume = "16",
number = "1",
pages = "34-37",
doi = "10.1021/ol4028557"
}

Vulović, B., Gruden-Pavlović, M., Matović, R.,& Saičić, R.. (2014). Substrate Stereocontrol in the Intramolecular Organocatalyzed Tsuji-Trost Reaction: Enantioselective Synthesis of Allokainates. in Organic Letters
Amer Chemical Soc, Washington., 16(1), 34-37.
https://doi.org/10.1021/ol4028557

Vulović B, Gruden-Pavlović M, Matović R, Saičić R. Substrate Stereocontrol in the Intramolecular Organocatalyzed Tsuji-Trost Reaction: Enantioselective Synthesis of Allokainates. in Organic Letters. 2014;16(1):34-37.
doi:10.1021/ol4028557 .

Vulović, Bojan, Gruden-Pavlović, Maja, Matović, Radomir, Saičić, Radomir, "Substrate Stereocontrol in the Intramolecular Organocatalyzed Tsuji-Trost Reaction: Enantioselective Synthesis of Allokainates" in Organic Letters, 16, no. 1 (2014):34-37,
https://doi.org/10.1021/ol4028557 . .

TY  - JOUR
AU  - Vulović, Bojan
AU  - Bihelović, Filip
AU  - Matović, Radomir
AU  - Saičić, Radomir
PY  - 2010
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1073
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Tetrahedron
T1  - Organocatalyzed Tsuji-Trost reaction: a new method for the closure of five- and six-membered rings (vol 65, pg 10485, 2009)
VL  - 66
IS  - 17
SP  - 3275
EP  - 3275
DO  - 10.1016/j.tet.2010.03.013
ER  - 

@article{
author = "Vulović, Bojan and Bihelović, Filip and Matović, Radomir and Saičić, Radomir",
year = "2010",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Tetrahedron",
title = "Organocatalyzed Tsuji-Trost reaction: a new method for the closure of five- and six-membered rings (vol 65, pg 10485, 2009)",
volume = "66",
number = "17",
pages = "3275-3275",
doi = "10.1016/j.tet.2010.03.013"
}

Vulović, B., Bihelović, F., Matović, R.,& Saičić, R.. (2010). Organocatalyzed Tsuji-Trost reaction: a new method for the closure of five- and six-membered rings (vol 65, pg 10485, 2009). in Tetrahedron
Pergamon-Elsevier Science Ltd, Oxford., 66(17), 3275-3275.
https://doi.org/10.1016/j.tet.2010.03.013

Vulović B, Bihelović F, Matović R, Saičić R. Organocatalyzed Tsuji-Trost reaction: a new method for the closure of five- and six-membered rings (vol 65, pg 10485, 2009). in Tetrahedron. 2010;66(17):3275-3275.
doi:10.1016/j.tet.2010.03.013 .

Vulović, Bojan, Bihelović, Filip, Matović, Radomir, Saičić, Radomir, "Organocatalyzed Tsuji-Trost reaction: a new method for the closure of five- and six-membered rings (vol 65, pg 10485, 2009)" in Tetrahedron, 66, no. 17 (2010):3275-3275,
https://doi.org/10.1016/j.tet.2010.03.013 . .

TY  - JOUR
AU  - Vulović, Bojan
AU  - Bihelović, Filip
AU  - Matović, Radomir
AU  - Saičić, Radomir
PY  - 2009
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1031
AB  - A combination of organotransition metal catalysis and organocatalysis allows for Tsuji-Trost 5-exo- and 6-exo-cyclizations of aldehydes. This transformation can also be accomplished as a catalytic asymmetric reaction, which affords vinylcyclopentane derivatives with up to 98%ee. (C) 2009 Elsevier Ltd. All rights reserved.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Tetrahedron
T1  - Organocatalyzed Tsuji-Trost reaction: a new method for the closure of five- and six-membered rings
VL  - 65
IS  - 50
SP  - 10485
EP  - 10494
DO  - 10.1016/j.tet.2009.10.006
ER  - 

@article{
author = "Vulović, Bojan and Bihelović, Filip and Matović, Radomir and Saičić, Radomir",
year = "2009",
abstract = "A combination of organotransition metal catalysis and organocatalysis allows for Tsuji-Trost 5-exo- and 6-exo-cyclizations of aldehydes. This transformation can also be accomplished as a catalytic asymmetric reaction, which affords vinylcyclopentane derivatives with up to 98%ee. (C) 2009 Elsevier Ltd. All rights reserved.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Tetrahedron",
title = "Organocatalyzed Tsuji-Trost reaction: a new method for the closure of five- and six-membered rings",
volume = "65",
number = "50",
pages = "10485-10494",
doi = "10.1016/j.tet.2009.10.006"
}

Vulović, B., Bihelović, F., Matović, R.,& Saičić, R.. (2009). Organocatalyzed Tsuji-Trost reaction: a new method for the closure of five- and six-membered rings. in Tetrahedron
Pergamon-Elsevier Science Ltd, Oxford., 65(50), 10485-10494.
https://doi.org/10.1016/j.tet.2009.10.006

Vulović B, Bihelović F, Matović R, Saičić R. Organocatalyzed Tsuji-Trost reaction: a new method for the closure of five- and six-membered rings. in Tetrahedron. 2009;65(50):10485-10494.
doi:10.1016/j.tet.2009.10.006 .

Vulović, Bojan, Bihelović, Filip, Matović, Radomir, Saičić, Radomir, "Organocatalyzed Tsuji-Trost reaction: a new method for the closure of five- and six-membered rings" in Tetrahedron, 65, no. 50 (2009):10485-10494,
https://doi.org/10.1016/j.tet.2009.10.006 . .

TY  - JOUR
AU  - Bihelović, Filip
AU  - Matović, Radomir
AU  - Vulović, Bojan
AU  - Saičić, Radomir
PY  - 2007
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/4357
AB  - Synergic combination of organotransition metal catalysis and organocatalysis allows, for the first time, the Tsuji-Trost cyclization of aldehydes. A catalytic asymmetric variant of the reaction is also possible.
PB  - American Chemical Society (ACS)
T2  - Organic Letters
T1  - Organocatalyzed cyclizations of π-allylpalladium complexes: A new method for the construction of five- and six-membered rings
VL  - 9
IS  - 24
SP  - 5063
EP  - 5066
DO  - 10.1021/ol7023554
ER  - 

@article{
author = "Bihelović, Filip and Matović, Radomir and Vulović, Bojan and Saičić, Radomir",
year = "2007",
abstract = "Synergic combination of organotransition metal catalysis and organocatalysis allows, for the first time, the Tsuji-Trost cyclization of aldehydes. A catalytic asymmetric variant of the reaction is also possible.",
publisher = "American Chemical Society (ACS)",
journal = "Organic Letters",
title = "Organocatalyzed cyclizations of π-allylpalladium complexes: A new method for the construction of five- and six-membered rings",
volume = "9",
number = "24",
pages = "5063-5066",
doi = "10.1021/ol7023554"
}

Bihelović, F., Matović, R., Vulović, B.,& Saičić, R.. (2007). Organocatalyzed cyclizations of π-allylpalladium complexes: A new method for the construction of five- and six-membered rings. in Organic Letters
American Chemical Society (ACS)., 9(24), 5063-5066.
https://doi.org/10.1021/ol7023554

Bihelović F, Matović R, Vulović B, Saičić R. Organocatalyzed cyclizations of π-allylpalladium complexes: A new method for the construction of five- and six-membered rings. in Organic Letters. 2007;9(24):5063-5066.
doi:10.1021/ol7023554 .

Bihelović, Filip, Matović, Radomir, Vulović, Bojan, Saičić, Radomir, "Organocatalyzed cyclizations of π-allylpalladium complexes: A new method for the construction of five- and six-membered rings" in Organic Letters, 9, no. 24 (2007):5063-5066,
https://doi.org/10.1021/ol7023554 . .

TY  - JOUR
AU  - Bihelović, Filip
AU  - Matović, Radomir
AU  - Vulović, Bojan
AU  - Saičić, Radomir
PY  - 2007
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/890
AB  - Synergic combination of organotransition metal catalysis and organocatalysis allows, for the first time, the Tsuji-Trost cyclization of aldehydes. A catalytic asymmetric variant of the reaction is also possible.
PB  - Amer Chemical Soc, Washington
T2  - Organic Letters
T1  - Organocatalyzed cyclizations of pi-allylpalladium complexes: A new method for the construction of five- and six-membered rings
VL  - 9
IS  - 24
SP  - 5063
EP  - 5066
DO  - 10.1021/ol7023554
ER  - 

@article{
author = "Bihelović, Filip and Matović, Radomir and Vulović, Bojan and Saičić, Radomir",
year = "2007",
abstract = "Synergic combination of organotransition metal catalysis and organocatalysis allows, for the first time, the Tsuji-Trost cyclization of aldehydes. A catalytic asymmetric variant of the reaction is also possible.",
publisher = "Amer Chemical Soc, Washington",
journal = "Organic Letters",
title = "Organocatalyzed cyclizations of pi-allylpalladium complexes: A new method for the construction of five- and six-membered rings",
volume = "9",
number = "24",
pages = "5063-5066",
doi = "10.1021/ol7023554"
}

Bihelović, F., Matović, R., Vulović, B.,& Saičić, R.. (2007). Organocatalyzed cyclizations of pi-allylpalladium complexes: A new method for the construction of five- and six-membered rings. in Organic Letters
Amer Chemical Soc, Washington., 9(24), 5063-5066.
https://doi.org/10.1021/ol7023554

Bihelović F, Matović R, Vulović B, Saičić R. Organocatalyzed cyclizations of pi-allylpalladium complexes: A new method for the construction of five- and six-membered rings. in Organic Letters. 2007;9(24):5063-5066.
doi:10.1021/ol7023554 .

Bihelović, Filip, Matović, Radomir, Vulović, Bojan, Saičić, Radomir, "Organocatalyzed cyclizations of pi-allylpalladium complexes: A new method for the construction of five- and six-membered rings" in Organic Letters, 9, no. 24 (2007):5063-5066,
https://doi.org/10.1021/ol7023554 . .