Vulović, Bojan

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Authority KeyName Variants
orcid::0000-0002-6293-2714
  • Vulović, Bojan (23)
  • Vulović, Ivana (1)
Projects

Author's Bibliography

Određivanje makro-elemenata u zemljištu i odgovarajućim saprobnim gljivama poreklom sa područja Crnog vrha (Niš)

Vulović, Ivana

(2020)

TY  - BOOK
AU  - Vulović, Ivana
PY  - 2020
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/4183
AB  - Određen je sadržaj makro-elemenata (Ca, Mg, K, Na i Fe) po fazama zemljišta da bi se procenila biodostupnost elemenata, i sadržaj makro-elemanta u pečurkama koje rastu na drveću, koje raste na analiziranom zemljištu. Na kraju su izračunati i biokoncentracioni faktori, kako bi se utvrdilo da li analizirane pečurke apsorbuju određene makro-elemente iz datih zemljišta.
T1  - Određivanje makro-elemenata u zemljištu i odgovarajućim saprobnim gljivama poreklom sa područja Crnog vrha (Niš)
SP  - 1
EP  - 26
ER  - 
@thesis{
author = "Vulović, Ivana",
year = "2020",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/4183",
abstract = "Određen je sadržaj makro-elemenata (Ca, Mg, K, Na i Fe) po fazama zemljišta da bi se procenila biodostupnost elemenata, i sadržaj makro-elemanta u pečurkama koje rastu na drveću, koje raste na analiziranom zemljištu. Na kraju su izračunati i biokoncentracioni faktori, kako bi se utvrdilo da li analizirane pečurke apsorbuju određene makro-elemente iz datih zemljišta.",
title = "Određivanje makro-elemenata u zemljištu i odgovarajućim saprobnim gljivama poreklom sa područja Crnog vrha (Niš)",
pages = "1-26"
}
Vulović, I. (2020). Određivanje makro-elemenata u zemljištu i odgovarajućim saprobnim gljivama poreklom sa područja Crnog vrha (Niš).
, 1-26.
Vulović I. Određivanje makro-elemenata u zemljištu i odgovarajućim saprobnim gljivama poreklom sa područja Crnog vrha (Niš). 2020;:1-26
Vulović Ivana, "Određivanje makro-elemenata u zemljištu i odgovarajućim saprobnim gljivama poreklom sa područja Crnog vrha (Niš)" (2020):1-26

Cyclization Reactions of Oxyallyl Cation. A Method for Cyclopentane Ring Formation

Vulović, Bojan; Trmčić, Milena; Matović, Radomir; Saičić, Radomir

(ACS, 2019)

TY  - JOUR
AU  - Vulović, Bojan
AU  - Trmčić, Milena
AU  - Matović, Radomir
AU  - Saičić, Radomir
PY  - 2019
UR  - http://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",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/3819",
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.
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. Organic Letters. 2019;21(23):9618-9621
Vulović Bojan, Trmčić Milena, Matović Radomir, Saičić Radomir, "Cyclization Reactions of Oxyallyl Cation. A Method for Cyclopentane Ring Formation" Organic Letters, 21, no. 23 (2019):9618-9621,
https://doi.org/10.1021/acs.orglett.9b03791 .
1
1

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

Vulović, Bojan; Trmčić, Milena; Matović, Radomir; Saičić, Radomir

(ACS, 2019)

TY  - BOOK
AU  - Vulović, Bojan
AU  - Trmčić, Milena
AU  - Matović, Radomir
AU  - Saičić, Radomir
PY  - 2019
UR  - http://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
ER  - 
@book{
author = "Vulović, Bojan and Trmčić, Milena and Matović, Radomir and Saičić, Radomir",
year = "2019",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/3841",
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"
}
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.
Organic Letters
ACS..
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. Organic Letters. 2019;
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" Organic Letters (2019)

Gold(I)-Catalyzed C-O/C-C Bond-Forming Domino Reactions and Their Synthetic Applications

Bihelović, Filip; Vulović, Bojan; Saičić, Radomir

(Wiley-V C H Verlag Gmbh, Weinheim, 2018)

TY  - JOUR
AU  - Bihelović, Filip
AU  - Vulović, Bojan
AU  - Saičić, Radomir
PY  - 2018
UR  - http://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",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/2156",
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.
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. Israel Journal of Chemistry. 2018;58(5):521-530
Bihelović Filip, Vulović Bojan, Saičić Radomir, "Gold(I)-Catalyzed C-O/C-C Bond-Forming Domino Reactions and Their Synthetic Applications" Israel Journal of Chemistry, 58, no. 5 (2018):521-530,
https://doi.org/10.1002/ijch.201700033 .
2
2
3

Synthesis of Natural Products and the Development of Synthetic Methodology: The Case Study of (-)-Atrop-abyssomicin C

Bihelović, Filip; Vulović, Bojan; Saičić, Radomir

(Natural Products Inc, Westerville, 2017)

TY  - JOUR
AU  - Bihelović, Filip
AU  - Vulović, Bojan
AU  - Saičić, Radomir
PY  - 2017
UR  - http://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
ER  - 
@article{
author = "Bihelović, Filip and Vulović, Bojan and Saičić, Radomir",
year = "2017",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/2512",
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"
}
Bihelović, F., Vulović, B.,& Saičić, R. (2017). Synthesis of Natural Products and the Development of Synthetic Methodology: The Case Study of (-)-Atrop-abyssomicin C.
Natural Product Communications
Natural Products Inc, Westerville., 12(8), 1209-1214.
Bihelović F, Vulović B, Saičić R. Synthesis of Natural Products and the Development of Synthetic Methodology: The Case Study of (-)-Atrop-abyssomicin C. Natural Product Communications. 2017;12(8):1209-1214
Bihelović Filip, Vulović Bojan, Saičić Radomir, "Synthesis of Natural Products and the Development of Synthetic Methodology: The Case Study of (-)-Atrop-abyssomicin C" Natural Product Communications, 12, no. 8 (2017):1209-1214
2
2

Palladium-Catalyzed Cross-Coupling of Silyl Electrophiles with Alkylzinc Halides: A Silyl-Negishi Reaction

Cinderella, Andrew P.; Vulović, Bojan; Watson, Donald A.

(Amer Chemical Soc, Washington, 2017)

TY  - JOUR
AU  - Cinderella, Andrew P.
AU  - Vulović, Bojan
AU  - Watson, Donald A.
PY  - 2017
UR  - http://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",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/2475",
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.
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. Journal of the American Chemical Society. 2017;139(23):7741-7744
Cinderella Andrew P., Vulović Bojan, Watson Donald A., "Palladium-Catalyzed Cross-Coupling of Silyl Electrophiles with Alkylzinc Halides: A Silyl-Negishi Reaction" Journal of the American Chemical Society, 139, no. 23 (2017):7741-7744,
https://doi.org/10.1021/jacs.7b04364 .
9
42
32
37

Heck-Like Reactions Involving Heteroatomic Electrophiles

Vulović, Bojan; Watson, Donald A.

(Wiley-V C H Verlag Gmbh, Weinheim, 2017)

TY  - JOUR
AU  - Vulović, Bojan
AU  - Watson, Donald A.
PY  - 2017
UR  - http://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",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/2525",
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.
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. European Journal of Organic Chemistry. 2017;(34):4996-5009
Vulović Bojan, Watson Donald A., "Heck-Like Reactions Involving Heteroatomic Electrophiles" European Journal of Organic Chemistry, no. 34 (2017):4996-5009,
https://doi.org/10.1002/ejoc.201700485 .
1
17
21
21

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

Cinderella, Andrew P.; Vulović, Bojan; Watson, Donald A.

(Amer Chemical Soc, Washington, 2017)

TY  - BOOK
AU  - Cinderella, Andrew P.
AU  - Vulović, Bojan
AU  - Watson, Donald A.
PY  - 2017
UR  - http://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
ER  - 
@book{
author = "Cinderella, Andrew P. and Vulović, Bojan and Watson, Donald A.",
year = "2017",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/3099",
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"
}
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.
Journal of the American Chemical Society
Amer Chemical Soc, Washington..
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. Journal of the American Chemical Society. 2017;
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" Journal of the American Chemical Society (2017)

Palladium-Catalyzed Cross-Coupling of Monochlorosilanes and Grignard Reagents

Vulović, Bojan; Cinderella, Andrew P.; Watson, Donald A.

(American Chemical Society, 2017)

TY  - JOUR
AU  - Vulović, Bojan
AU  - Cinderella, Andrew P.
AU  - Watson, Donald A.
PY  - 2017
UR  - http://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",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/3923",
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.
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. ACS Catalysis. 2017;7(12):8113-8117
Vulović Bojan, Cinderella Andrew P., Watson Donald A., "Palladium-Catalyzed Cross-Coupling of Monochlorosilanes and Grignard Reagents" ACS Catalysis, 7, no. 12 (2017):8113-8117,
https://doi.org/10.1021/acscatal.7b03465 .
25
20
23

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

Vulović, Bojan; Cinderella, Andrew P.; Watson, Donald A.

(American Chemical Society, 2017)

TY  - BOOK
AU  - Vulović, Bojan
AU  - Cinderella, Andrew P.
AU  - Watson, Donald A.
PY  - 2017
UR  - http://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
ER  - 
@book{
author = "Vulović, Bojan and Cinderella, Andrew P. and Watson, Donald A.",
year = "2017",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/3924",
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"
}
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.
ACS Catalysis
American Chemical Society..
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. ACS Catalysis. 2017;
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" ACS Catalysis (2017)

Palladium-Catalyzed Cross-Coupling of Monochlorosilanes and Grignard Reagents

Vulović, Bojan; Cinderella, Andrew P.; Watson, Donald A.

(American Chemical Society, 2017)

TY  - JOUR
AU  - Vulović, Bojan
AU  - Cinderella, Andrew P.
AU  - Watson, Donald A.
PY  - 2017
UR  - http://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",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/3925",
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.
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. ACS Catalysis. 2017;7(12):8113-8117
Vulović Bojan, Cinderella Andrew P., Watson Donald A., "Palladium-Catalyzed Cross-Coupling of Monochlorosilanes and Grignard Reagents" ACS Catalysis, 7, no. 12 (2017):8113-8117,
https://doi.org/10.1021/acscatal.7b03465 .
25
20
23

Gold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (-)-Gabosine H and (-)-6-epi-Gabosine H

Vulović, Bojan; Kolarski, Dušan; Bihelović, Filip; Matović, Radomir; Gruden-Pavlović, Maja; Saičić, Radomir

(Amer Chemical Soc, Washington, 2016)

TY  - JOUR
AU  - Vulović, Bojan
AU  - Kolarski, Dušan
AU  - Bihelović, Filip
AU  - Matović, Radomir
AU  - Gruden-Pavlović, Maja
AU  - Saičić, Radomir
PY  - 2016
UR  - http://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",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/2290",
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.
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. Organic Letters. 2016;18(15):3886-3889
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" Organic Letters, 18, no. 15 (2016):3886-3889,
https://doi.org/10.1021/acs.orglett.6b01898 .
11
12
11
13

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)

Vulović, Bojan; Kolarski, Dušan; Bihelović, Filip; Matović, Radomir; Gruden-Pavlović, Maja; Saičić, Radomir

(Amer Chemical Soc, Washington, 2016)

TY  - JOUR
AU  - Vulović, Bojan
AU  - Kolarski, Dušan
AU  - Bihelović, Filip
AU  - Matović, Radomir
AU  - Gruden-Pavlović, Maja
AU  - Saičić, Radomir
PY  - 2016
UR  - http://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",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/2327",
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).
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). Organic Letters. 2016;18(19):5186-5187
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)" Organic Letters, 18, no. 19 (2016):5186-5187,
https://doi.org/10.1021/acs.orglett.6b02509 .
2

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

Vulović, Bojan; Kolarski, Dušan; Bihelović, Filip; Matović, Radomir; Gruden-Pavlović, Maja; Saičić, Radomir

(Amer Chemical Soc, Washington, 2016)

TY  - BOOK
AU  - Vulović, Bojan
AU  - Kolarski, Dušan
AU  - Bihelović, Filip
AU  - Matović, Radomir
AU  - Gruden-Pavlović, Maja
AU  - Saičić, Radomir
PY  - 2016
UR  - http://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
ER  - 
@book{
author = "Vulović, Bojan and Kolarski, Dušan and Bihelović, Filip and Matović, Radomir and Gruden-Pavlović, Maja and Saičić, Radomir",
year = "2016",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/3520",
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"
}
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.
Organic Letters
Amer Chemical Soc, Washington..
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. Organic Letters. 2016;
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" Organic Letters (2016)

Synthesis of vinyldihydropyran by cooperative catalysis

Vulović, Bojan; Marić, Ivana; Matović, Radomir; Saičić, Radomir

(Serbian Chemical Soc, Belgrade, 2016)

TY  - JOUR
AU  - Vulović, Bojan
AU  - Marić, Ivana
AU  - Matović, Radomir
AU  - Saičić, Radomir
PY  - 2016
UR  - http://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",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/2388",
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.
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. Journal of the Serbian Chemical Society. 2016;81(12):1335-1343
Vulović Bojan, Marić Ivana, Matović Radomir, Saičić Radomir, "Synthesis of vinyldihydropyran by cooperative catalysis" Journal of the Serbian Chemical Society, 81, no. 12 (2016):1335-1343,
https://doi.org/10.2298/JSC161102103V .
1
1

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

Vulović, Bojan; Marić, Ivana; Matović, Radomir; Saičić, Radomir

(Serbian Chemical Soc, Belgrade, 2016)

TY  - BOOK
AU  - Vulović, Bojan
AU  - Marić, Ivana
AU  - Matović, Radomir
AU  - Saičić, Radomir
PY  - 2016
UR  - http://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
ER  - 
@book{
author = "Vulović, Bojan and Marić, Ivana and Matović, Radomir and Saičić, Radomir",
year = "2016",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/3629",
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"
}
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.
Journal of the Serbian Chemical Society
Serbian Chemical Soc, Belgrade..
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. Journal of the Serbian Chemical Society. 2016;
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" Journal of the Serbian Chemical Society (2016)

Kooperativna kataliza: kombinacija organokatalize i katalize kompleksima prelaznih metala i njena primena u totalnoj sintezi alokainata

Vulović, Bojan

(Универзитет у Београду, Хемијски факултет, 2014)

TY  - BOOK
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  - http://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.
ER  - 
@phdthesis{
author = "Vulović, Bojan",
year = "2014",
url = "http://eteze.bg.ac.rs/application/showtheses?thesesId=3263, https://fedorabg.bg.ac.rs/fedora/get/o:11666/bdef:Content/download, http://vbs.rs/scripts/cobiss?command=DISPLAY&base=70036&RID=47669775, http://nardus.mpn.gov.rs/123456789/5904, http://cherry.chem.bg.ac.rs/handle/123456789/2689",
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."
}
Vulović, B. (2014). Synergistic catalysis: combination of organocatalysis and organotransition-meta catalysis and application in total synthesis of allokainates..
Универзитет у Београду
Универзитет у Београду, Хемијски факултет..
Vulović B. Synergistic catalysis: combination of organocatalysis and organotransition-meta catalysis and application in total synthesis of allokainates.. Универзитет у Београду. 2014;
Vulović Bojan, "Synergistic catalysis: combination of organocatalysis and organotransition-meta catalysis and application in total synthesis of allokainates." Универзитет у Београду (2014)

Kooperativna kataliza: kombinacija organokatalize i katalize kompleksima prelaznih metala i njena primena u totalnoj sintezi alokainata

Vulović, Bojan

(Универзитет у Београду, Хемијски факултет, 2014)

TY  - BOOK
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  - http://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.
ER  - 
@phdthesis{
author = "Vulović, Bojan",
year = "2014",
url = "http://eteze.bg.ac.rs/application/showtheses?thesesId=3263, https://fedorabg.bg.ac.rs/fedora/get/o:11666/bdef:Content/download, http://vbs.rs/scripts/cobiss?command=DISPLAY&base=70036&RID=47669775, http://nardus.mpn.gov.rs/123456789/5904, http://cherry.chem.bg.ac.rs/handle/123456789/2690",
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."
}
Vulović, B. (2014). Synergistic catalysis: combination of organocatalysis and organotransition-meta catalysis and application in total synthesis of allokainates..
Универзитет у Београду
Универзитет у Београду, Хемијски факултет..
Vulović B. Synergistic catalysis: combination of organocatalysis and organotransition-meta catalysis and application in total synthesis of allokainates.. Универзитет у Београду. 2014;
Vulović Bojan, "Synergistic catalysis: combination of organocatalysis and organotransition-meta catalysis and application in total synthesis of allokainates." Универзитет у Београду (2014)

Substrate Stereocontrol in the Intramolecular Organocatalyzed Tsuji-Trost Reaction: Enantioselective Synthesis of Allokainates

Vulović, Bojan; Gruden-Pavlović, Maja; Matović, Radomir; Saičić, Radomir

(Amer Chemical Soc, Washington, 2014)

TY  - JOUR
AU  - Vulović, Bojan
AU  - Gruden-Pavlović, Maja
AU  - Matović, Radomir
AU  - Saičić, Radomir
PY  - 2014
UR  - http://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",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/1475",
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.
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. Organic Letters. 2014;16(1):34-37
Vulović Bojan, Gruden-Pavlović Maja, Matović Radomir, Saičić Radomir, "Substrate Stereocontrol in the Intramolecular Organocatalyzed Tsuji-Trost Reaction: Enantioselective Synthesis of Allokainates" Organic Letters, 16, no. 1 (2014):34-37,
https://doi.org/10.1021/ol4028557 .
7
7
7

Organocatalyzed Tsuji-Trost reaction: a new method for the closure of five- and six-membered rings (vol 65, pg 10485, 2009)

Vulović, Bojan; Bihelović, Filip; Matović, Radomir; Saičić, Radomir

(Pergamon-Elsevier Science Ltd, Oxford, 2010)

TY  - JOUR
AU  - Vulović, Bojan
AU  - Bihelović, Filip
AU  - Matović, Radomir
AU  - Saičić, Radomir
PY  - 2010
UR  - http://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",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/1073",
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).
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). Tetrahedron. 2010;66(17):3275-3275
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)" Tetrahedron, 66, no. 17 (2010):3275-3275,
https://doi.org/10.1016/j.tet.2010.03.013 .
4
7
3

Organocatalyzed Tsuji-Trost reaction: a new method for the closure of five- and six-membered rings

Vulović, Bojan; Bihelović, Filip; Matović, Radomir; Saičić, Radomir

(Pergamon-Elsevier Science Ltd, Oxford, 2009)

TY  - JOUR
AU  - Vulović, Bojan
AU  - Bihelović, Filip
AU  - Matović, Radomir
AU  - Saičić, Radomir
PY  - 2009
UR  - http://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",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/1031",
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.
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. Tetrahedron. 2009;65(50):10485-10494
Vulović Bojan, Bihelović Filip, Matović Radomir, Saičić Radomir, "Organocatalyzed Tsuji-Trost reaction: a new method for the closure of five- and six-membered rings" Tetrahedron, 65, no. 50 (2009):10485-10494,
https://doi.org/10.1016/j.tet.2009.10.006 .
54
43
49

Organocatalyzed cyclizations of π-allylpalladium complexes: A new method for the construction of five- and six-membered rings

Bihelovic, F.; Matović, Radomir; Vulović, Bojan; Saičić, Radomir N.

(American Chemical Society (ACS), 2007)

TY  - JOUR
AU  - Bihelovic, F.
AU  - Matović, Radomir
AU  - Vulović, Bojan
AU  - Saičić, Radomir N.
PY  - 2007
UR  - http://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 = "Bihelovic, F. and Matović, Radomir and Vulović, Bojan and Saičić, Radomir N.",
year = "2007",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/4357",
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"
}
Bihelovic, F., Matović, R., Vulović, B.,& Saičić, R. N. (2007). Organocatalyzed cyclizations of π-allylpalladium complexes: A new method for the construction of five- and six-membered rings.
Organic Letters
American Chemical Society (ACS)., 9(24), 5063-5066.
https://doi.org/10.1021/ol7023554
Bihelovic F, Matović R, Vulović B, Saičić RN. Organocatalyzed cyclizations of π-allylpalladium complexes: A new method for the construction of five- and six-membered rings. Organic Letters. 2007;9(24):5063-5066
Bihelovic F., Matović Radomir, Vulović Bojan, Saičić Radomir N., "Organocatalyzed cyclizations of π-allylpalladium complexes: A new method for the construction of five- and six-membered rings" Organic Letters, 9, no. 24 (2007):5063-5066,
https://doi.org/10.1021/ol7023554 .
107
90
94

Erratum: Organocatalyzed Cyclizations of pi-allylpalladium complexes: A new method for the construction of five- and six-membered rings (vol 9, pg 5064, 2007)

Bihelović, Filip; Matović, Radomir; Vulović, Bojan; Saičić, Radomir

(Amer Chemical Soc, Washington, 2007)

TY  - JOUR
AU  - Bihelović, Filip
AU  - Matović, Radomir
AU  - Vulović, Bojan
AU  - Saičić, Radomir
PY  - 2007
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/894
PB  - Amer Chemical Soc, Washington
T2  - Organic Letters
T1  - Erratum: Organocatalyzed Cyclizations of pi-allylpalladium complexes: A new method for the construction of five- and six-membered rings (vol 9, pg 5064, 2007)
VL  - 9
IS  - 26
SP  - 5649
EP  - 5649
DO  - 10.1021/ol702760g
ER  - 
@article{
author = "Bihelović, Filip and Matović, Radomir and Vulović, Bojan and Saičić, Radomir",
year = "2007",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/894",
publisher = "Amer Chemical Soc, Washington",
journal = "Organic Letters",
title = "Erratum: Organocatalyzed Cyclizations of pi-allylpalladium complexes: A new method for the construction of five- and six-membered rings (vol 9, pg 5064, 2007)",
volume = "9",
number = "26",
pages = "5649-5649",
doi = "10.1021/ol702760g"
}
Bihelović, F., Matović, R., Vulović, B.,& Saičić, R. (2007). Erratum: Organocatalyzed Cyclizations of pi-allylpalladium complexes: A new method for the construction of five- and six-membered rings (vol 9, pg 5064, 2007).
Organic Letters
Amer Chemical Soc, Washington., 9(26), 5649-5649.
https://doi.org/10.1021/ol702760g
Bihelović F, Matović R, Vulović B, Saičić R. Erratum: Organocatalyzed Cyclizations of pi-allylpalladium complexes: A new method for the construction of five- and six-membered rings (vol 9, pg 5064, 2007). Organic Letters. 2007;9(26):5649-5649
Bihelović Filip, Matović Radomir, Vulović Bojan, Saičić Radomir, "Erratum: Organocatalyzed Cyclizations of pi-allylpalladium complexes: A new method for the construction of five- and six-membered rings (vol 9, pg 5064, 2007)" Organic Letters, 9, no. 26 (2007):5649-5649,
https://doi.org/10.1021/ol702760g .
3
3
2

Organocatalyzed cyclizations of pi-allylpalladium complexes: A new method for the construction of five- and six-membered rings

Bihelović, Filip; Matović, Radomir; Vulović, Bojan; Saičić, Radomir

(Amer Chemical Soc, Washington, 2007)

TY  - JOUR
AU  - Bihelović, Filip
AU  - Matović, Radomir
AU  - Vulović, Bojan
AU  - Saičić, Radomir
PY  - 2007
UR  - http://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",
url = "http://cherry.chem.bg.ac.rs/handle/123456789/890",
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.
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. Organic Letters. 2007;9(24):5063-5066
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" Organic Letters, 9, no. 24 (2007):5063-5066,
https://doi.org/10.1021/ol7023554 .
107
90
94