The conjugate addition of nitroalkanes to electron-poor alkenes is a widely used process
which only in the late nineties of the last century has efficiently evolved in its asymmetric …

Highly efficient drug‐delivery tools for membrane‐impermeable compounds, proteins, and
nucleic acids in living cells are useful in the fields of chemical biology and drug discovery …

X-ray crystallography has been applied to the structural analysis of a series of tetrapeptides
that were previously assessed for catalytic activity in an atroposelective bromination …

There has been growing interest in performing organocatalysis within a supramolecular
system as a means of controlling reaction reactivity and stereoselectivity. Here, a protein is …

The isothiourea-catalysed enantioselective Michael addition of 3-aryloxindole and 4-
substituted-dihydropyrazol-3-one pronucleophiles to α, β-unsaturated p-nitrophenyl esters is …

Published data on the preparation methods, properties and chemical transformations of
linear-and cross-conjugated enynones are integrated. The molecular and crystal structures …

A site‐divergent stereoselective Michael reaction system is developed based on the
identification of two distinct catalysts. Cinchonidine‐derived thiourea catalyzes the 1, 4 …

Enzymes are predominantly proteins able to effectively and selectively catalyze highly
complex biochemical reactions in mild reaction conditions. Nevertheless, they are limited to …

Cell-penetrating peptides are receiving increasing attention as drug delivery tools, and the
search for peptides with high cell-penetrating ability and negligible cytotoxicity has become …

Aromatic nitro compounds play a unique role in the synthesis of drugs and pharmaceutically
oriented molecules. This field of organic chemistry continues to be in demand and relevant …