1.
Org Lett
; 26(20): 4212-4217, 2024 May 24.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38743309
RESUMO
An unusual rhodium-catalyzed C-H activation/Lossen rearrangement/oxa-Michael addition tandem cyclization has been achieved along with a tunable well-known C-H activation/[4 + 2] annulation, leading to regio-, chemo-, and diastereoselective access to diverse pentacyclic α-carbolines and ß-carboline-1-one derivatives in moderate to good yields with significant anticancer activity.