Olefin migratory insertion into a metal-hydrogen or a metal-carbon bond is
an ubiquitous step in olefin coordination catalysis by transition metal com
plexes. When the catalytic system has element(s) of chirality, and when the
two carbon atoms of the substrate are not symmetry-related, the nature of
the reaction products will be determined by the capacity of the catalytic s
ystem for enantioface selection and by the direction of the insertion. Desp
ite some progress having been made, good control of this important catalyti
c step is far from being realized. Considerations concerning this step are
presented with particular reference to the work of the author in the field
of hydrocarbonylation and olefin (co)polymerization reactions.