Launching Werner Complexes into the Modern Era of Catalytic Enantioselective Organic Synthesis.

Reactions catalyzed by transition metal complexes almost always entail binding of one or more reactants to the metal center, and nearly every corner of the "chiral pool" has been picked over in efforts to develop enantioselective catalysts. As reported by Alfred Werner in 1911-1912, salts of the formally -symmetric [Co(en)] trication (en = ethylenediamine) were among the first chiral inorganic compounds to be resolved into enantiomers. These air- and water-stable complexes are substitution-inert, so for 100 years they languished without application in organic synthesis.