Facile synthesis of diverse hetero polyaromatic hydrocarbons (PAHs) via the styryl Diels-Alder reaction of conjugated diynes

The styryl dehydro-Diels-Alder reaction with a conjugated diyne is reported. While typical alkyne-styrene condensation requires elevated temperatures (>160 degrees C), the application of a conjugated diyne allowed for effective transformation under milder conditions (80 degrees C). The thermally stable triazole-gold (TA-Au) catalyst further improved the reaction yields (up to 95%), producing the desired alkynyl-naphthalene in a single step with molecular oxygen as the oxidant. Sequential alkyne activation resulted in various polyaromatic hydrocarbons (PAHs) in excellent yields, highlighting the efficiency of this new strategy for the preparation of PAHs with good functional group tolerance and structural diversity.

Automated summary

The styryl dehydro-Diels-Alder reaction with a conjugated diyne is reported, which allows for effective transformation under milder conditions and produces high yields.