Conia-ene annulation of the α-cyano ß-TMS-capped alkynyl cycloalkanone system and its synthetic application.

Under catalysis with ZnI(2), an effective annulation process of ω-silylacetylenic α-cyano ketones, leading to the formation of various bicyclic frameworks characterized with a TMS-containing methylenecyclopentane ring, has been developed.

Autoxidative annulation cascade of the α-cyano ß-TMS-capped alkynyl cycloalkanone system.

The autoxidative annulation cascade promoted by an α-cyano ß-TMS-capped alkynyl cycloalkanone system under catalysis with pyridine in one oxygen atmosphere has proven to be highly viable. On the basis of this newly developed protocol, a variety of highly functionalized bicyclic frameworks can be effectively constructed.