In this review, we highlight the use of organic photoredox catalysts in a myriad of synthetic transformations with a range of applications. This overview is arranged by catalyst class where the photophysics and electrochemical characteristics of each is discussed to underscore the differences and advantages to each type of single electron redox agent. We highlight both net reductive and oxidative as well as redox neutral transformations that can be accomplished using purely organic photoredox-active catalysts. An overview of the basic photophysics and electron transfer theory is presented in order to provide a comprehensive guide for employing this class of catalysts in photoredox manifolds.

Organic Photoredox Catalysis

N-Heterocyclic Carbenes in Late Transition Metal Catalysis

Asymmetric enamine catalysis.

Reactions that convert carbon–hydrogen (C–H) bonds into carbon–carbon (C–C) or carbon–heteroatom (C–Y) bonds are attractive tools for organic chemists, potentially expediting the synthesis of target molecules through new disconnections in retrosynthetic analysis. Despite extensive inorganic and organometallic study of the insertion of homogeneous metal species into unactivated C–H bonds, practical applications of this technology in organic chemistry are still rare. Only in the past decade have metal-catalyzed C–H functionalization reactions become more widely utilized in organic synthesis.Research in the area of homogeneous transition metal–catalyzed C–H functionalization can be broadly grouped into two subfields. They reflect different approaches and goals and thus have different challenges and opportunities. One approach involves reactions of completely unfunctionalized aromatic and aliphatic hydrocarbons, which we refer to as “first functionalization”. Here the substrates are nonpolar and hydrophobic a...

Weak coordination as a powerful means for developing broadly useful C-H functionalization reactions.

Small-molecule H-bond donors in asymmetric catalysis.

A New Powerful and Practical BLA Catalyst for Highly Enantioselective Diels−Alder Reaction: An Extreme Acceleration of Reaction Rate by Brønsted Acid

Il est possible d'effectuer une addition -1,4 ou -1,2 nucleophile de reactifs organoaluminiques a des acetals chiraux d'enaldehydes ce qui fournit un acces facile a des aldehydes β-substitues ou des alcools allyliques, respectivement, sous forme optiquement active

Unprecedented regio- and stereochemical control in the addition of organoaluminum reagents to chiral α,β-unsaturated acetals

Trimethylsilyl pentafluorophenylbis(trifluoromethanesulfonyl)methide as a super Lewis acid catalyst for the condensation of trimethylhydroquinone with isophytol.

Modification of the Wittig reaction to permit the stereospecific synthesis of certain trisubstituted olefins. Stereospecific synthesis of .alpha.-santalol

Hisashi Yamamoto

Papers

A New Powerful and Practical BLA Catalyst for Highly Enantioselective Diels−Alder Reaction: An Extreme Acceleration of Reaction Rate by Brønsted Acid

Unprecedented regio- and stereochemical control in the addition of organoaluminum reagents to chiral α,β-unsaturated acetals

Trimethylsilyl pentafluorophenylbis(trifluoromethanesulfonyl)methide as a super Lewis acid catalyst for the condensation of trimethylhydroquinone with isophytol.

Modification of the Wittig reaction to permit the stereospecific synthesis of certain trisubstituted olefins. Stereospecific synthesis of .alpha.-santalol

Asymmetric cyclization of unsaturated aldehydes catalyzed by a chiral lewis acid