Abstract Site-selective C (sp3)–H arylation is an appealing strategy to synthesize complex
arene structures but remains a challenge facing synthetic chemists. Here we report the use …

The CH bond functionalization represents one of the most efficient and straightforward
strategies to diversify the existing molecules. It is the most challenging task to achieve the …

We report a general approach for efficient deuteration of the metabolically labile α-C–H
bonds of widespread amides and amines. Temporarily masking the secondary amine group …

While selective defunctionalizations are valuable in organic synthesis, hydrodeamination of
primary amines poses challenges. Deuterodeamination, analogous to hydrodeamination …

Aryl-substituted aliphatic amines are widely recognized as immensely valuable molecules.
Consequently, the development of practical strategies for the construction of these …

Deuteration, using diverse, readily accessible deuterium reagents, has recently emerged as
a powerful tool for achieving high deuterium content with precise positional control …

Deuterated molecules are of growing interest because of the specific characteristics of
deuterium, such as stronger C‐D bonds being stronger than C‐H bonds. Polyethylene …