A photoinduced arene-alkyne [3 + 2] cycloaddition cascade of 1-alkynylnaphthalen-2-ols for tunable synthesis of skeletally diverse bridged hexacycles

Photoinduced arene-alkyne [3 + 2] cycloaddition cascades of 1-alkynylnaphthalen-2-ols without a photosensitizer were developed for the first time, enabling tunable synthesis of skeletally diverse bridged hexacyclic architectures with good yields and complete stereoselectivities through solvent-dependent divergent dearomatized cyclodimerizations. The photocatalysis in N,N-dimethylformamide (DMF) delivered functionalized bicyclo[3.2.1]octane-containing bridged oxa-heterocycles, whereas tetrahydrofuran (THF) oriented high stereoselectivity to offer bridged carbocycles. The reaction pathway generates two classes of complex three-dimensional structures that evolve from the same planar internal alkynes.