C–H activation has surfaced as an increasingly powerful tool for molecular sciences, with
notable applications to material sciences, crop protection, drug discovery, and …

Diazabicyclo [5.4. 0] undec-7-ene (DBU) has received a significant importance in organic
synthesis during recent years because of its interesting ability to catalyze organic reaction …

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 …

Density functional calculations have provided evidence that a Ag (I)-mediated
deconstructive fluorination of N-benzoylated cyclic amines (LH) with Selectfluor [(F …

DFT calculations have been combined with experiments to study the mechanism of γ-C
(sp3)–H arylation of aliphatic amines promoted by palladium–glyoxylic acid cooperative …

A novel oxidative cross-coupling of benzo [b] thiophene 1, 1-dioxides with arylboronic acids
was reported. The efficient reaction occurred at the C2-position via C–H activation, followed …

An efficient and novel protocol was developed for a Cu‐catalyzed Ullmann‐type aryl alkyl
ether synthesis by reacting various (hetero) aryl halides (Cl, Br, I) with alcohols as active …

An efficient Rh (III)-catalyzed cross-dehydrogenative coupling of N-pyridinylindoles with
benzo [b] thiophene 1, 1-dioxides has been developed through directing-group-assisted C …

A feasible one-pot synthesis of dimerized arene and heteroarene systems was achieved by
employing 2 mol% of Co (II) catalyst 1 along with Zn dust at room temperature in 2–4 h. The …

Regioselective B–H activation of o-carboranes is an effective way for constructing o-
carborane derivatives, which have broad applications in medicine, catalysis and the wider …