Evgeniya O. Dorofeeva

TL;DR: In this article, the electrocatalytic reaction smoothly proceeds under neutral and mild conditions with aromatic aldehydes bearing both electron-donating and electron-withdrawing groups.

TL;DR: In this article, the combined electrolysis of barbituric acids and benzylidenemalononitriles or benylidenecyanoacetates in methanol in an undivided cell in the presence of sodium bromide results in efficient MIRC (Michael-initiated ring closure) formation of corresponding spirocyclopropylbarbiturates in 45-93% yield.

TL;DR: In this paper, the most promising methods for the synthesis of functionally substituted cyclopropanes, namely, the electrocatalytic cascade and multicomponent transformations of CH acids and also the joint electrolysis of CH acid and activated alkenes or carbonyl compounds in the presence of alkali metal halides as mediators, are discussed.

TL;DR: In this article, a unique stereoselective cascade electrocatalytic process has been found, which opens an efficient and convenient way to synthesize (R*,R*)-bis(spiro-2,4-dihydro-3H-pyrazol-3-one)cyclopropanes.

TL;DR: In this paper, the synthesis of spirobarbiturates containing furo[2,3-d]pyrimidine scaffold was applied to the formation of medicinally relevant compounds with prominent pharmacological and physiological activity.