Electrochemistry represents one of the most intimate ways of interacting with molecules. This
review discusses advances in synthetic organic electrochemistry since 2000. Enabling …

Conventional methods for carrying out carbon–hydrogen functionalization and carbon–
nitrogen bond formation are typically conducted at elevated temperatures, and rely on …

Imines are versatile synthetic intermediates in a variety of organic transformations and are
essential pharmacophores in numerous biologically active compounds.[1] Great progress …

1, 2-Cyclic sulfamidates undergo efficient and regiospecific nucleophilic cleavage with 2-
bromophenols (and related anilines and thiophenols), followed by Pd (0)-mediated …

In the presence of a catalytic amount of radical initiator AIBN, primary amines are oxidatively
coupled to imines and tertiary amines are cyanated to α-aminonitriles. These “metal-free” …

Recent efforts to design synthetic quinone-based catalysts for the efficient aerobic oxidation
of amines to imines have been inspired by copper amine oxidases (CuAOs), a family of …

An electrochemical N-acylation of carboxylic acids with amines was reported. The
sustainable TBAB electrocatalysis proceeded with excellent chemoselectivity and positional …

Environmentally friendly oxidation of primary aliphatic amines to imines has been
successfully achieved, under metal‐free conditions, by the use of diverse electrogenerated o …

This review includes information for around two last decades on cycloaddition reactions of
enamines with various agents in order to build carbo‐and heterocycles. In addition, the …

Benzimidazole belongs to the top five most commonly used five-membered aromatic
nitrogen heterocycles among US FDA approved pharmaceuticals. Over the last few years, a …