The investigation of new oxidative transformations for the synthesis of carbon–heteroatom
and heteroatom–heteroatom bonds is of fundamental importance in the synthesis of …

The iodination of organic compounds is of great importance in synthetic organic chemistry. It
opens comprehensive approaches for the synthesis of various biologically active …

An azidation method for C–N bond formation at benzylic C–H positions is described using
copper-catalyzed visible light photochemistry and the Zhdankin azidoiodinane reagent. The …

Aliphatic amides are selectively functionalized at the γ-and δ-positions through directed
radical 1, 5 and 1, 6 H-abstractions, respectively. The initially formed γ-or δ-lactams are …

A room-temperature, copper-catalyzed amination of primary benzylic C− H bonds with
primary and secondary sulfonamides is described. The reaction is applicable to the coupling …

The first example of a practical and selective azidation of unactivated aliphatic C–H bonds
with easily handled sulfonyl azides as azide source without the use of transition metals has …

Nitrogen-containing compounds, which are found in a wide range of natural products,
material science, and pharmaceuticals, have attracted the interest of many chemists due to …

We report a direct azidation of benzylic C (sp3)− H bonds via an electrochemical process,
which use cheap and durable graphite plates as electrodes, without any external oxidants or …

A double functionalization of vicinal sp 3 C–H bonds has been developed, wherein a β
amine and γ iodide are incorporated onto an aliphatic alcohol in a single operation. This …

Sodium periodate and sodium azide combination has been found to be an excellent reagent
system suitable for the direct diazidation of styrenes, alkenes, benzylic alcohols, and aryl …