The Povarov reaction provides a straightforward and modular entry to 1, 2, 3, 4-
tetrahydroquinolines (THQs). Despite its importance, it was only very recently that several …

Synthesis of substituted 1,2,3,4-tetrahydroquinones by the Povarov reaction. New potentials
of the classical reaction Page 1 Russian Chemical Reviews Synthesis of substituted 1,2,3,4tetrahydroquinones …

An efficient method for the construction of furanobenzodihydropyran skeletons has been
developed through Pd-catalyzed asymmetric decarboxylative cycloaddition of vinylethylene …

Catalytic asymmetric Povarov protocols have undergone an explosive growth, especially in
the last ten years, since the first example was published in 1996. The use of chiral Lewis and …

As demonstrated by earlier successes with enamines, nitrogen-activated C= C double
bonds have considerable potential for use in the construction of various nitrogen-containing …

An efficient natural product inspired diversity oriented syn thesis of tetrahydroquinoline
analogues has been developed using the natural carbohydrate derived solid acid catalyst …

Domino catalysis: We have developed the first enantioselective domino Mannich–
ketalization reaction of o‐hydroxy benzaldimines with electron‐rich alkenes (see scheme) …

A catalytic asymmetric aza-Michael− Michael addition cascade of anilines to nitroolefin
enoates in the presence of chiral bifunctional thiourea catalysts has been disclosed. This …

A methodology is reported for preparing amides using amines as an acyl source. The
protocol involves the visible-light-promoted oxidative amidation of amines with pyrazole to …

An efficient method for the enantio‐and diastereoselective formation of furanochromanones
has been developed via Pd‐catalyzed asymmetric allylic cycloaddition of vinylethylene …