Dearomatization reactions provide rapid access to structurally complex three-dimensional
molecules from simple aromatic compounds. Plenty of reports have demonstrated their …

Electrochemistry, which employs electrons as reagents and avoids the use of traditional
redox reagents, becomes a powerful tool in oxidative dehydrogenation cross-coupling …

The field in dearomatization of aromatic compounds for the construction of spirocycle
compounds has been developed rapidly over the last two decades and it provides …

An electrochemical dearomatizing spirocyclization of alkynes with dimethyl 2-
benzylmalonates for the preparation of spiro [4.5] deca-trienones has been developed. This …

The dearomatization of aromatic compounds is an important synthetic strategy used in
accessing complex three‐dimensional structures from simple aromatic precursors. This …

Visible light mediated functionalizations have significantly expanded the scope of alkynes by
unraveling new mechanistic pathways and enabling their transformation to diverse structural …

Dearomatization reactions involving radical cyclizations can facilitate the synthesis of
complex polycyclic systems that find applications in medicinal chemistry and natural product …

Visible-light-induced dearomatization reaction via energy-transfer mechanism is an
emerging strategy for the synthesis of highly strained polycyclic molecules. Transient, high …

The construction of diverse sp3‐rich skeletal ring systems is of importance to drug discovery
programmes and natural product synthesis. Herein, we report the photocatalytic construction …

Visible light promoted difunctionalization of alkynes is reviewed. The difunctionalization
reaction is achieved by different reagents. Radicals such as carbon (sp 3), carbon (sp 2) …