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 …

Carbon–hydrogen bond functionalizations provide an attractive method for streamlining
organic synthesis, and many strategies have been developed for conducting these …

As one type of chromene, 2H-chromenes represent important oxygen heterocycles, which
not only widely exist in natural products, pharmaceutical agents and biologically relevant …

The oxa-Pictet–Spengler reaction is arguably the most straightforward and modular way to
construct the privileged isochroman motif, but its scope is largely limited to benzaldehyde …

The first organocatalytic enantioselective C H alkenylation and arylation reactions of N‐
carbamoyl tetrahydropyridines and tetrahydro‐β‐carbolines (THCs) are described. The …

Over the past few years, the development of oxidative methodologies towards efficient and
selective direct Csp3–H bond functionalization processes has attracted tremendous …

The cobalt-catalyzed cross-dehydrogenative coupling of (benz) oxazoles and ethers is
described. Access to some important bioactive heteroaryl ether derivatives was achieved …

An oxidative cross-dehydrogenative coupling (CDC) of isoquinolines with methyl arenes has
been developed, allowing for the facile synthesis of a broad range of structurally diverse C1 …

Ligands H4sal-dag (I) and H4Brsal-dag (II) derived from 1, 3-diaminoguanidine and
salicylaldehyde or 5-bromosalicylaldehyde react with one or 2 mol equivalent of vanadium …