1.
Org Biomol Chem
; 22(3): 466-471, 2024 Jan 17.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38099332
RESUMO
A ruthenium-catalyzed C-H alkylation/cyclization sequence is presented to prepare silyl indenes with atom and step-economy. This domino reaction is triggered by acyl silane-directed C-H activation, and an aldehyde controlled the following enol cyclization/condensation other than ß-H elimination. The protocol tolerates a broad substitution pattern, and the further synthetic elaboration of silyl indenes allows access to a diverse range of interesting indene and indanone derivatives.