As two coexisting and fast-growing research fields in modern synthetic chemistry, the
merging of organocatalysis and C–H bond functionalization is well foreseeable, and the joint …

C− C bond formation is a fundamental transformation in organic synthesis. The development
of new synthetic methodology could be considered as a way of pursuing a novel method for …

Oxygen‐containing heterocycles are an important class of compounds with diverse
biological activities. In recent years, direct α‐C–H functionalization of inexpensive and …

Abstract Manganese‐catalyzed C H functionalization reactions of ketimines set the stage
for the expedient synthesis of cis‐β‐amino acid esters through site‐and regioselective …

The first one‐pot enantioselective oxidative coupling of cyclic benzylic ethers with aldehydes
has been developed. A variety of benzylic ethers were transformed into the corresponding …

The first catalytic asymmetric cross-dehydrogenative coupling of cyclic carbamates and
terminal alkynes has been established. The reaction features high enantiocontrol and …

Manganese‐catalysed reactions have attracted great attention recently due to the high
relative abundance and cheap and eco‐friendly behaviour. Applications of manganese …

A versatile manganese (I) catalyst was employed in C H aminocarbonylation reactions of
heteroarenes with aryl as well as with alkyl isocyanates using a removable directing group …

Acceptorless dehydrogenative coupling reactions has emerged as one of the promising
technique in synthetic organic chemistry to construct carbon‐carbon and carbon‐heteroatom …

Selenides are important structural motifs with a broad range of biological activities and
versatile transformational abilities. In this study, a novel and mild method was developed for …