Chem Catalysis, Journal Year: 2025, Volume and Issue: unknown, P. 101359 - 101359
Published: April 1, 2025
Language: Английский
Chem Catalysis, Journal Year: 2025, Volume and Issue: unknown, P. 101359 - 101359
Published: April 1, 2025
Language: Английский
Organic Letters, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 28, 2025
We have realized a cathodic deoxygenative alkylation between nitro(hetero)arenes and organic halides, employing bis(pinacolato)diboron (B2pin2) LiCl as additives to trap stabilize the generated alkyl radicals carbanions, thereby facilitating efficient N-O cleavage selective C-N bond formation. The protocol offers an economical method for synthesis of multiple aromatic(hetero) amines, without need reactive reductants exclusion air moisture. Notably, is distinguished by scalability, broad functional group compatibility, safe mild conditions, demonstrating practicality in late-stage modification various bioactive compounds.
Language: Английский
Citations
0Chem Catalysis, Journal Year: 2025, Volume and Issue: unknown, P. 101359 - 101359
Published: April 1, 2025
Language: Английский
Citations
0