Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Prabhakar Kale A"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 20, Iss 1, Pp 2500-2566 (2024)
With the resurgence of electrosynthesis in organic chemistry, there is a significant increase in the number of routes available for late-stage functionalization (LSF) of drugs. Electrosynthetic methods, which obviate the need for hazardous chemical o
Externí odkaz:
https://doaj.org/article/2745ebade9bf424e819040911e05c332
Autor:
Yi, Liang, Kong, Deshen, Prabhakar Kale, Ajit, Alshehri, Rawan, Yue, Huifeng, Gizatullin, Amir, Maity, Bholanath, Kancherla, Rajesh, Cavallo, Luigi, Rueping, Magnus
Publikováno v:
Angewandte Chemie International Edition; 12/16/2024, Vol. 63 Issue 51, p1-9, 9p
Publikováno v:
JACS Au, Vol 1, Iss 7, Pp 1057-1065 (2021)
Externí odkaz:
https://doaj.org/article/29477eaf00a3479eb81d5a0a62edf955
Publikováno v:
Tropical Ecology.
Autor:
Prabhakar Kale, Ajit1 (AUTHOR), Nikolaienko, Pavlo1 (AUTHOR), Smirnova, Kristina1 (AUTHOR), Rueping, Magnus1 (AUTHOR) magnus.rueping@kaust.edu.sa
Publikováno v:
European Journal of Organic Chemistry. 6/25/2021, Vol. 2021 Issue 24, p3496-3500. 5p.
Publikováno v:
European Journal of Organic Chemistry. 26
Publikováno v:
European Journal of Organic Chemistry. 2021:3496-3500
Publikováno v:
JACS Au, Vol 1, Iss 7, Pp 1057-1065 (2021)
A nickel-catalyzed cross-coupling amination with weak nitrogen nucleophiles is described. Aryl halides as well as aryl tosylates can be efficiently coupled with a series of weak N-nucleophiles, including anilines, sulfonamides, sulfoximines, carbamat
Publikováno v:
Chemistry – A European Journal. 25:7177-7184
A hydrogen atom transfer-directed electrochemical intramolecular C-H amination has been developed in which the N-radical species are generated at the anode, and the base required for the reaction is generated at the cathode. A broad range of valuable
Publikováno v:
Organic & Biomolecular Chemistry. 13:10995-11002
A new approach has been developed for the synthesis of substituted 2-alkenyl-3-arylindoles. The strategy comprises palladium-catalyzed dual α-arylation of TES-enol ethers of enones as the key step. This methodology results in products with very good