Organocatalytic domino/cascade reactions provide a convenient method for the construction
of complex molecular structures bearing multiple stereocenters in a highly stereoselective …

Can green chemistry be the right reading key to let organocatalyst design take a step
forward towards sustainable catalysis? What if the intriguing chemistry promoted by more …

The prevalence of nitrogen containing heterocycles in natural products and pharmaceuticals
is a doubtless fact. In this review, recent applications of a stereoselective aza-Michael …

Cyrene™ as a bio-alternative dipolar aprotic solvent: a waste minimizing and molar efficient
protocol for the synthesis of amides from acid chlorides and primary amines in the bio …

The asymmetric conjugate addition of carbon and heteroatom nucleophiles to nitroalkenes
is a very interesting tool for the construction of highly functionalized synthetic building …

The asymmetric catalytic 1, 6-addition of p-QMs with racemic oxindoles under the
bifunctional catalysis of C2-symmetric dimeric Cinchona-derived squaramide is described …

The first example of enantioselective S− H insertion reactions of sulfoxonium ylides is
reported. Under the influence of thiourea catalysis, excellent levels of enantiocontrol (up to …

The development of noncovalent halogen bonding (XB) catalysis is rapidly gaining traction,
as isolated reports documented better performance than the well-established hydrogen …

The first example of organocatalytic enantioselective C–H insertion reactions of indoles and
sulfoxonium ylides is reported. Under the influence of phosphoric acid catalysis, levels of …

An unprecedented asymmetric catalytic tandem aminolysis/aza-Michael addition reaction of
spirocyclic para-dienoneimides has been designed and developed through organocatalytic …