The emergence of modern photocatalysis, characterized by mildness and selectivity, has
significantly spurred innovative late-stage C–H functionalization approaches that make use …

Direct photocatalyzed hydrogen atom transfer (d-HAT) can be considered a method of
choice for the elaboration of aliphatic C–H bonds. In this manifold, a photocatalyst (PCHAT) …

Photoredox chemistry with organic or transition metal agents has been reviewed in earlier
years, but such is the pace of progress that we will overlap very little with earlier …

Abstract C (sp 3)-rich bicyclic hydrocarbon scaffolds, as exemplified by bicyclo [1.1. 1]
pentanes, play an increasingly high-profile role as saturated bioisosteres of benzenoids in …

Compared with general redox chemistry, electrochemistry using the electron as a potent,
controllable, yet traceless alternative to chemical oxidants/reductants usually offers more …

Herein, we report a new class of electrophotocatalysts, polycyclic aromatic hydrocarbons,
that promote the reduction of unactivated carbonyl compounds to generate versatile ketyl …

Photocatalysis opens up a new window for carbonyl chemistry. Despite a multitude of
photochemical reactions of carbonyl compounds, visible light-induced catalytic asymmetric …

Ketone–olefin coupling reactions are common methods for the formation of carbon–carbon
bonds. This reaction class typically requires stoichiometric or super stoichiometric quantities …

In contrast to the extensive but non-recyclable use of tetraalkoxydiboron (4) compounds as
stoichiometric reagents in diverse reactions, this article reports an atom-economical reaction …

The molecular editing of ketones represents an appealing strategy due to its ability to
maximize the structural diversity of ketone compounds in a straightforward manner …