Photochemical C–H Borylation in Organic Synthesis
Supriya Rej, Stephanie G. E. Amos, Arjan W. Kleij
Abstract
High Resolution Image Download MS PowerPoint Slide Although C–H bond functionalization has been extensively studied since its discovery in 1955, the borylation of organic compounds by activating C–H bonds only became popular since the valuable discovery by Hartwig in 1995 who considered a wider application of these transformations in synthetic organic chemistry. For C–H borylation, catalytic activation of this generally low-reactivity bond can be performed in many ways. Among the approaches reported are the use and application of stoichiometric reagents, thermal activation, and photochemical activation of suitable substrates. Iridium-, ruthenium-, and rhodium-based catalytic protocols using thermal activation have played a crucial role toward the establishment of this area. Photochemical activation, though, has only been scarcely explored despite the fact that it represents a comparably environmentally benign protocol using light as a renewable energy source. In this literature survey, we highlight the recent developments in photochemical C–H borylation from its initial inception up to the latest advancements.