The efficacy and synthetic versatility of asymmetric organocatalysis have contributed
enormously to the field of organic synthesis since the early 2000s. As asymmetric …

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

Bifunctional squaramides have emerged as powerful hydrogen‐bonding catalysts for
promoting a wide array of useful asymmetric reactions, which provides convenient methods …

The organocatalytic enantioselective decarboxylative addition of malonic acid half thioesters
to ketimines derived from isatins by using N‐heteroarenesulfonyl cinchona alkaloid amides …

Nitroalkanes and nitroalkenes have been always considered as convenient and readily
available intermediates in organic synthesis, including total synthesis of natural products. 1 …

Catalytic decarboxylative reactions are attractive as biomimetic reactions and
environmentally friendly reaction processes. In this review, the origin and recent …

In this work we introduce a sustainable membrane-based synthesis–separation platform for
enantioselective organocatalysis. An azido derivatized cinchona-squaramide bifunctional …

This review examines recent advances in asymmetric catalytic decarboxylative addition
reactions which have become a powerful method to form C C and C X bond using …

In this study, water was demonstrated to be an exceptionally efficient reaction medium for
the noncovalent, hydrogen-bonding-promoted enantioselective Michael addition of …

A bifunctional squaramide catalyzed sulfa-Michael/aldol cascade reaction between 1, 4-
dithiane-2, 5-diol and chalcones with a low catalyst loading has been developed …