Alcohols are abundant and attractive feedstock molecules for organic synthesis. Many
methods for their functionalization require them to first be converted into a more activated …

A robust and practical protocol for preparing alkyl aryl ethers has been developed, which
relies on using two types of ligands to promote Cu-catalyzed alkoxylation of (hetero) aryl …

Abstract A highly effective C− O coupling reaction of (hetero) aryl electrophiles with primary
and secondary alcohols is reported. Catalyzed by a NiII‐aryl complex under long‐wave UV …

Phenols, anilines, and malonates have been arylated under metal‐free conditions with
twelve aryl (phenyl) iodonium salts in a systematic chemoselectivity study. A new “anti‐ortho …

The formation of aryl‐alkyl ether bonds through cross coupling of alcohols with aryl halides
represents a useful strategic departure from classical SN2 methods. Numerous tactics …

The C single bond O bond-forming reactions are important in organic synthesis due to the
presence of these bonds in numerous natural products, biologically important compounds …

An efficient procedure for palladium-catalyzed coupling reactions of (hetero) aryl bromides
and chlorides with primary aliphatic alcohols has been developed. Key to the success is the …

Aryl alkyl ethers are present in many naturally occurring and medicinally relevant
compounds.[1] Copper [2]-and palladiumcatalyzed CÀO bond-forming reactions have …

Decarboxylative Chan–Evans–Lam-type couplings are presented as a new strategy for the
regiospecific construction of diaryl and alkyl aryl ethers starting from easily available …

An efficient Cu-catalyzed one-pot approach for the synthesis of unsymmetrical diaryl
thioethers using potassium ethyl xanthogenate as a thiol surrogate is developed. This new …