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

Organosilicon reagents are highly versatile and privileged scaffolds in modern synthetic
chemistry, largely due to the range of transformations the groups are amenable to. The β …

2, 3-Dichloro-5, 6-dicyano-1, 4-benzoquinone (DDQ) is a highly effective reagent for
promoting C–H bond functionalization. The oxidative cleavage of benzylic and allylic C–H …

Efficient Indirect Electrochemical Synthesis of 2‐Substituted Benzoxazoles using Sodium Iodide
as Mediator - Li - 2013 - Advanced Synthesis & Catalysis - Wiley Online Library Skip to Article …

N‐Heterocycles have been found in a large number of natural products, drug molecules,
and bioactive compounds, and they thereby play a vital role in diverse research disciplines …

The classical Prins cyclization reaction has been one of the most studied reactions during
the last two decades and it has found many applications in key steps of natural product …

An efficient method for the construction of fluorinated benzo [a] quinolizidines from α‐
trifluoromethyl alkenes and dihydroisoquinoline acetic acids using visible light …

Vinyl sulfides react rapidly and efficiently with 2, 3-dichloro-5, 6-dicyano-1, 4-benzoquinone
(DDQ) to form α, β-unsaturated thiocarbenium ions through oxidative carbon–hydrogen …

Chromenes and isochromenes react quickly with 2, 3-dichloro-5, 6-dicyano-1, 4-
benzoquinone (DDQ) to form persistent aromatic oxocarbenium ions through oxidative …

Numerous hydride‐abstracting agents generate the same cationic intermediate, but
substrate features such as intermediate cation stability, oxidation potential, and steric …