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  - THES
AU  - Jović, Miloš
PY  - 2021
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/4648
AB  - U ovom master radu reakcijom nukleofilne aromatične supstitucije sintetisan je N-(1-fenil-1H-tetrazol-5-il)piridin-2-amin 23, u niskom prinosu, polazeći od 5-bromo-1-fenil-1H-tetrazola 22 i 2-aminopiridina. Nizak prinos verovatno je posledica raspada 5-bromo-1-fenil-1H-tetrazola 22 u baznoj sredini. Primenom Buchwald-Hartwigove reakcije izvršeno je N-arilovanje 5-fenil-1,3,4-tiadiazol-2-amina 21 sa 2-brompiridinom, pri čemu nastaje 5-fenil-N-(piridin-2-il)-1,3,4-tiadiazol-2-amin 24 u niskom prinosu. U ovom slučaju nizak prinos je posledica prisustva 2-aminopiridinskog motiva u polaznom jedinjenju, kao i u proizvodu, koji usled velike koordinacione sposobnosti dovodi do inhibicije katalitičkog ciklusa.
T1  - 2-Aminopiridin u reakcijama C(sp2)-N ukrštenog kuplovanja
SP  - 1
EP  - 24
UR  - https://hdl.handle.net/21.15107/rcub_cherry_4648
ER  - 

@mastersthesis{
author = "Jović, Miloš",
year = "2021",
abstract = "U ovom master radu reakcijom nukleofilne aromatične supstitucije sintetisan je N-(1-fenil-1H-tetrazol-5-il)piridin-2-amin 23, u niskom prinosu, polazeći od 5-bromo-1-fenil-1H-tetrazola 22 i 2-aminopiridina. Nizak prinos verovatno je posledica raspada 5-bromo-1-fenil-1H-tetrazola 22 u baznoj sredini. Primenom Buchwald-Hartwigove reakcije izvršeno je N-arilovanje 5-fenil-1,3,4-tiadiazol-2-amina 21 sa 2-brompiridinom, pri čemu nastaje 5-fenil-N-(piridin-2-il)-1,3,4-tiadiazol-2-amin 24 u niskom prinosu. U ovom slučaju nizak prinos je posledica prisustva 2-aminopiridinskog motiva u polaznom jedinjenju, kao i u proizvodu, koji usled velike koordinacione sposobnosti dovodi do inhibicije katalitičkog ciklusa.",
title = "2-Aminopiridin u reakcijama C(sp2)-N ukrštenog kuplovanja",
pages = "1-24",
url = "https://hdl.handle.net/21.15107/rcub_cherry_4648"
}

Jović, M.. (2021). 2-Aminopiridin u reakcijama C(sp2)-N ukrštenog kuplovanja. , 1-24.
https://hdl.handle.net/21.15107/rcub_cherry_4648

Jović M. 2-Aminopiridin u reakcijama C(sp2)-N ukrštenog kuplovanja. 2021;:1-24.
https://hdl.handle.net/21.15107/rcub_cherry_4648 .

Jović, Miloš, "2-Aminopiridin u reakcijama C(sp2)-N ukrštenog kuplovanja" (2021):1-24,
https://hdl.handle.net/21.15107/rcub_cherry_4648 .

TY  - THES
AU  - Jović, Miloš
PY  - 2020
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/4065
AB  - U opštem delu, prikazan je pregled literature koji obuhvata opšte osobine pirimidina i njegov biomedicinski značaj, primenu Pd-katalizovanih reakcija ukrštenog kuplovanja na 2,4-dihlorpirimidinu za formiranje C(sp2)-C(sp2) i C(sp2)-NH2 veze, kao i reakciju nukleofilne aromatične supstitucije sa aminima.
U našim radovima prikazana je, sinteza N-(1-benzil-1H-tetrazol-5-il)-2-hlorpirimidin-4-amina primenom Buchwald-Hartwigove reakcije, i dalja derivatizacija nukleofilnom aromatičnom supstitucijom sa aminima.
U eksperimentalnom delu, detaljno su opisani sinteza N-(1-benzil-1H-tetrazol-5-il)-2-hlorpirimidin-4-amina kao i procedura za nukleofilnu aromatičnu supstituciju sa 3-(dimetilamino)propil-aminom i pirolidinom.
T1  - Transformacije 2,4-dihlorpirimidina
SP  - 1
EP  - 24
UR  - https://hdl.handle.net/21.15107/rcub_cherry_4065
ER  - 

@misc{
author = "Jović, Miloš",
year = "2020",
abstract = "U opštem delu, prikazan je pregled literature koji obuhvata opšte osobine pirimidina i njegov biomedicinski značaj, primenu Pd-katalizovanih reakcija ukrštenog kuplovanja na 2,4-dihlorpirimidinu za formiranje C(sp2)-C(sp2) i C(sp2)-NH2 veze, kao i reakciju nukleofilne aromatične supstitucije sa aminima.
U našim radovima prikazana je, sinteza N-(1-benzil-1H-tetrazol-5-il)-2-hlorpirimidin-4-amina primenom Buchwald-Hartwigove reakcije, i dalja derivatizacija nukleofilnom aromatičnom supstitucijom sa aminima.
U eksperimentalnom delu, detaljno su opisani sinteza N-(1-benzil-1H-tetrazol-5-il)-2-hlorpirimidin-4-amina kao i procedura za nukleofilnu aromatičnu supstituciju sa 3-(dimetilamino)propil-aminom i pirolidinom.",
title = "Transformacije 2,4-dihlorpirimidina",
pages = "1-24",
url = "https://hdl.handle.net/21.15107/rcub_cherry_4065"
}

Jović, M.. (2020). Transformacije 2,4-dihlorpirimidina. , 1-24.
https://hdl.handle.net/21.15107/rcub_cherry_4065

Jović M. Transformacije 2,4-dihlorpirimidina. 2020;:1-24.
https://hdl.handle.net/21.15107/rcub_cherry_4065 .

Jović, Miloš, "Transformacije 2,4-dihlorpirimidina" (2020):1-24,
https://hdl.handle.net/21.15107/rcub_cherry_4065 .