Recently the fruitful merger of organoboron chemistry and photocatalysis has come to the
forefront of organic synthesis, resulting in the development of new technologies to access …

Synthesis of bicyclic scaffolds has attracted growing interest because they are of high
importance in modern pharmaceutical development. Here we report a strategy to access …

Organoboron chemistry has become a cornerstone of modern synthetic methodology. Most
of these reactions use an organoboron starting material that contains just one C (sp 2)–B or …

In pursuit of potent pharmaceutical candidates and to further improve their chemical traits,
small ring systems can serve as a potential starting point. Small ring units have the …

Saturated bicyclic compounds make up a valuable class of building blocks in the
development of agrochemicals and pharmaceuticals. Here, we present the synthesis of …

Cyclopropanes bearing contiguous all-carbon quaternary centers continue to attract
attention due to their bioactivities. However, methods to obtain cyclopropanes with …

Alkenylboronates are versatile building blocks for stereocontrolled synthesis owing to the
traceless nature of the boron group that can be leveraged to achieve highly selective …

Sensitized triplet–triplet annihilation upconversion is a promising strategy to use visible light
for chemical reactions requiring the energy input of UV photons. This strategy avoids unsafe …

A strategy for the photosensitized cycloaddition of alkenylboronates and allylic alcohols by a
temporary coordination is presented. The process allows for the synthesis of a diverse range …

Multicomponent domino reactions via electrochemical annulations have emerged as a
robust strategy for the rapid assembly of heterocyclics. Herein, an electrochemical …