The direct difunctionalization of alkenes, a cheap and abundant feedstock, represents one of
the most attractive strategies for increasing molecular complexity in synthetic organic …

Palladium-catalyzed aerobic oxidation reactions have been the focus of industrial
application and extensive research efforts for nearly 60 years. A significant transition …

1, 2-Dicarbofunctionalization of alkenes has emerged as an efficient synthetic strategy for
preparing substituted molecules by coupling readily available alkenes with electrophiles …

Transition metal (TM)‐catalyzed difunctionalization of unactivated olefins with two carbon‐
based entities is a powerful method to construct complex molecular architectures rapidly …

Alkenes, ethers, and alcohols account for a significant percentage of bulk reagents available
to the chemistry community. The petrochemical, pharmaceutical, and agrochemical …

Multi-site functionalization of molecules provides a potent approach to accessing intricate
compounds. However, simultaneous functionalization of the reactive site and the inert …

The difunctionalization of carbon–carbon double bonds, introducing two novel functional
groups onto both sides of the carbon–carbon bond in one pot, has become more and more …

Transition-metal-catalyzed dicarbofunctionalization of alkenes involving intramolecular Heck
cyclization followed by intermolecular cross-coupling has emerged as a powerful engine for …

Conspectus Efficient construction of ubiquitous carbon–carbon bonds between two
electrophiles has garnered interest in recent decades, particularly if it is mediated by …

The development of catalytic reactions of alkenes transformed the chemical industry in the
mid-20th century. Representative reactions included hydrogenation, oxidation …