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 …

Transition-metal-catalyzed reactions have been studied since the very beginning of the past
century and represent a great success in organic chemistry, along with the birth and growth …

The area of direct asymmetric functionalization of inert C–H bonds has attracted
considerable attention in recent years. To realize this type of challenging but promising …

The addition of a variety of radicals to the double bond of N-(arylsulfonyl) acrylamides can
trigger cyclization/aryl migration/desulfonylation cascades via amidyl radical intermediates …

An unprecedented dioxygen-triggered oxidative radical process was explored using
dioxygen as the solely terminal oxidant, realizing aerobic oxidaitve difunctionalization of …

For green and sustainable chemistry, molecular oxygen is considered as an ideal oxidant
due to its natural, inexpensive, and environmentally friendly characteristics, and therefore …

A comparative mechanistic study of Cu-catalyzed oxidative coupling reactions of N-
phenyltetrahydroisoquinoline with different nucleophiles was conducted. Two previously …

Dearomatization of indoles provides efficient synthetic routes for substituted indolines. In
most cases, indoles serve as nucleophiles. Reported here is an asymmetric dearomatization …

The Cu-catalyzed novel aerobic oxidative esterification reaction of 1, 3-diones for the
synthesis of α-ketoesters has been developed. This method combines C–C σ-bond …

A versatile aerobic catalytic system (I2 and O2/TBHP) for C–H functionalization is reported.
This CDC (cross-dehydrogentive coupling) reaction is compatible with a large number of …