Silylium-Ion-Promoted (3 + 2) Annulation of Allenylsilanes with Internal Alkynes Involving a Pentadienyl-to-Allyl Cation Electrocyclization

Abstract

A (3 + 2) annulation of allenyl- and, after rapid isomerization, propargylsilanes with internal 1-aryl-1-alkynes to form 4-methylenecyclopentenes is reported. The reaction is initiated by a silylium ion, and the catalytic cycle is subsequently maintained by the self-regeneration of the silylium-ion promoter. Unlike the well-established Danheiser annulation, where the allenylsilane serves as a three-carbon synthon , the present transformation engages the allenylsilane as a two-carbon synthon . Experimental observations and DFT calculations unveil a reaction cascade involving various β-silicon-stabilized carbocations, where a pentadienyl-to-allyl cation electrocyclization is the key step.DFG, 490737079, Hauptgruppen-Metall-vermittelte Hydrierungsreaktionen und KatalyseTU Berlin, Open-Access-Mittel – 202