1.
Org Lett
; 24(38): 6940-6944, 2022 09 30.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36129217
RESUMO
An efficacious method for building fluorovinyl spiro-[imidazole-indene] and α-amino-ß-naphthalenone skeletons synchronously has been shown to consist of Rh(III)-catalyzed C-H functionalization between 2H-imidazoles and difluoromethylene alkynes. This protocol demonstrates a practical and straightforward route for installing fluorine elements in the envisioned position of heterocyclic compounds.