Asymmetric catalysis is a major theme
of research in contemporary
synthetic organic chemistry. The discovery of general strategies for
highly enantioselective photochemical reactions, however, has been
a relatively recent development, and the variety of photoreactions
that can be conducted in a stereocontrolled manner is consequently
somewhat limited. Asymmetric photocatalysis is complicated by the
short lifetimes and high reactivities characteristic of photogenerated
reactive intermediates; the design of catalyst architectures that
can provide effective enantiodifferentiating environments for these
intermediates while minimizing the participation of uncontrolled racemic
background processes has proven to be a key challenge for progress
in this field. This review provides a summary of the chiral catalyst
structures that have been studied for solution-phase asymmetric photochemistry,
including chiral organic sensitizers, inorganic chromophores, and
soluble macromolecules. While some of these photocatalysts are derived
from privileged catalyst structures that are effective for both ground-state
and photochemical transformations, others are structural designs unique
to photocatalysis and offer insight into the logic required for highly
effective stereocontrolled photocatalysis.