Transition metal-catalyzed synthesis of 13α-estrone derivatives with potential anticancer properties

Synthesis of 3-(N,N-dimethylcarbamoyl)-13α-estrone and its 17-deoxy counterpart has been carried out. The dimethylcarbamoyl directing group enabled the regioselective ortho arylation of the steroidal starting compounds. The microwave-assisted, palladium-catalyzed phenylations led to 2-substituted 13...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Traj Péter
Abdolkhaliq Ali Hazhmat
Németh Anett
Dajcs Sámuel Trisztán
Zupkó István
Mernyák Erzsébet
Testületi szerző: International Symposium on Analytical and Environmental Problems (26.) (2020) (Szeged)
Dokumentumtípus: Könyv része
Megjelent: 2020
Sorozat:Proceedings of the International Symposium on Analytical and Environmental Problems 26
Kulcsszavak:Gyógyszerkémia, Analitikai kémia
Tárgyszavak:
Online Access:http://acta.bibl.u-szeged.hu/74032
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520 3 |a Synthesis of 3-(N,N-dimethylcarbamoyl)-13α-estrone and its 17-deoxy counterpart has been carried out. The dimethylcarbamoyl directing group enabled the regioselective ortho arylation of the steroidal starting compounds. The microwave-assisted, palladium-catalyzed phenylations led to 2-substituted 13α-estrones in a one-pot, tandem process. The Suzuki-Miyaura cross coupling reactions of the carbamates with phenylboronic acid resulted in 3-phenyl-3-deoxy13α-estrone. Certain newly synthesized compounds displayed potent antiproliferative action against human reproductive cancer cell lines of gynecological origin. 
650 4 |a Természettudományok 
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695 |a Gyógyszerkémia, Analitikai kémia 
700 0 1 |a Abdolkhaliq Ali Hazhmat  |e aut 
700 0 1 |a Németh Anett  |e aut 
700 0 1 |a Dajcs Sámuel Trisztán  |e aut 
700 0 1 |a Zupkó István  |e aut 
700 0 1 |a Mernyák Erzsébet  |e aut 
710 |a International Symposium on Analytical and Environmental Problems (26.) (2020) (Szeged) 
856 4 0 |u http://acta.bibl.u-szeged.hu/74032/1/proceedings_of_isaep_2020_338-341.pdf  |z Dokumentum-elérés