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 …

Electrochemical dearomative spirocyclization serves as a green and sustainable approach
to convert the flat, two‐dimension aromatic feedstock into the value‐added three‐dimension …

A novel and efficient strategy for trifluoromethylthiolation and dearomatization of activated
alkynes with stable and readily available AgSCF3 has been developed. Reported herein is …

Electrooxidative-induced synthesis of structurally diverse seleno-dibenzocyclohepten-5-
ones and seleno-spiro [5.5] trienones by selenylative carbannulation of biaryl ynones with …

A remarkable growth in hypervalent iodine‐mediated oxidative transformations as
stoichiometric reagents as well as catalysts has been well‐documented due to their …

A mild and convenient visible-light-induced method has been developed for the construction
of 3-sulfonyl and 3-sulfenyl azaspiro [4, 5] trienones through metal-free difunctionalization of …

A strategy to functionalized spiro [4.5] trienones, by domino silver-catalyzed decarboxylative
acylation or alkylation/ipso-cyclization of N-arylpropiolamides with α-keto acids/alkyl …

We developed a green method for the synthesis of spiro [4.5] trienones through an
electrochemical oxidative halocyclization with N-aryl alkynamides. This reaction was …

A novel and green route has been developed for the electrochemical synthesis of spiro [4.5]
trienones through radical‐initiated dearomative spirocyclization of alkynes with diselenides …

An electrochemical monofluoroalkylation cyclization of N-arylacrylamides to synthesize
monofluorinated 2-oxindoles has been developed, which employs common dimethyl 2 …