Pregled bibliografske jedinice broj: 1199903
Mechanochemical catalyst- and additive-free halogenation and imidation of azobenzenes with strong electron-donating substituents
Mechanochemical catalyst- and additive-free halogenation and imidation of azobenzenes with strong electron-donating substituents // 10th International Conference on Mechanochemistry and Mechanical Alloying : Book of Abstracts
Cagliari, Italija, 2022. str. 76-76 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 1199903 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Mechanochemical catalyst- and additive-free
halogenation and imidation of azobenzenes with
strong electron-donating substituents
Autori
Barišić, Dajana ; Pajić, Mario ; Halasz, Ivan ; Babić, Darko ; Ćurić, Manda
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
10th International Conference on Mechanochemistry and Mechanical Alloying : Book of Abstracts
/ - , 2022, 76-76
Skup
10th International Conference on Mechanochemistry and Mechanical Alloying (INCOME2022)
Mjesto i datum
Cagliari, Italija, 06.06.2022. - 10.06.2022
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
mechanochemistry ; halogenation ; imidation ; catalyst-free ; additive-free
Sažetak
Halogenated arenes are important precursors in cross-coupling reactions and components of numerous organic and natural compounds, pharmaceuticals, new materials, etc. Although ball milling methods are widely used for the synthesis of various classes of compounds, their application in the synthesis of halogenated arenes is still scarce. In this work, we present a catalyst- and additive- free protocol for the halogenation of 4, 4’- functionalized electron-rich azobenzenes in a ball mill under NG conditions, using N-halosuccinimides as a halogen source. These transformations resulted in the products halogenated in ortho- position to the electron-donating groups, while the reactions of azobenzenes containing dimethylamino group as substituent with NIS led to imidation products. The protocols described above provide a mild and environmentally friendly approach for the halogenation of Csp2–H bonds and the imidation of Csp3–H bonds of azobenzenes with electron-donating substituents by electrophilic activation using N-halosuccinimides.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
HRZZ-IP-2019-04-9951 - Mehanokemijska aktivacija i funkcionalizacija veze C–H potaknuta paladijem i usmjerena ligandom (MECHEMFUN) (Ćurić, Manda, HRZZ ) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb
Profili:
Ivan Halasz (autor)
Dajana Barišić (autor)
Mario Pajić (autor)
Manda Ćurić (autor)
Darko Babić (autor)