Radical modulated regioselective difunctionalization of vinyl enynes: tunable access to naphthalen-1(2H)-ones and allenic alcohols

A novel and efficient radical-modulated difunctionalization of vinyl enynes has been disclosed using TEMPO as a radical regulator. Facile access to structurally diverse 3-bromo-naphthalen-1(2H)-ones and 4-bromo-allenic alcohols was realized via 1,2-addition/1,2-migration or 1,4-addition, respectively. This protocol represents the first example of radical-modulated metal-free difunctionalization of 1,3-enynes with high regioselectivity.

Automated summary

A novel and efficient radical-modulated difunctionalization of vinyl enynes has been achieved using TEMPO as a radical regulator, resulting in structurally diverse products. This represents the first example of metal-free difunctionalization of 1,3-enynes with high regioselectivity.