The difunctionalization of carbon–carbon double bonds, introducing two novel functional
groups onto both sides of the carbon–carbon bond in one pot, has become more and more …

Iodine reagents have been identified as economically and ecologically benign alternatives
to transition metals, although their application as molecular catalysts in challenging C H …

The oxidative aminative vicinal difunctionalization of alkenes or related chemical feedstocks
has emerged as sustainable and multipurpose strategies that can efficiently construct two …

This review discusses the origins of iodine-mediated oxidation catalysis and gives a
comprehensive overview on this young field of research. The focus is set on oxidative C–X …

A novel method for the oxidative radical azidation of alkenes relies on an azide in
combination with a hypervalent iodine reagent. A cascade of C N and C C bond‐forming …

A copper-catalyzed aminoazidation of unactivated alkenes is achieved for the synthesis of
versatile unsymmetrical 1, 2-diamine derivatives. This transformation offers an effective …

Copper(II)/Iron(III) Co-catalyzed Intermolecular Diamination of Alkynes: Facile Synthesis of
Imidazopyridines | Organic Letters ACS ACS Publications C&EN CAS Find my institution Log In …

Palladium catalysis has been instrumental in the development of the intramolecular
diamination of alkenes. Reagent combinations of a palladium catalyst and iodosobenzene …

Vicinal diamines constitute one the most important functional motif in organic chemistry
because of its wide occurrence in a variety of biological and pharmaceutical molecules. We …

Conditions for an attractive and productive protocol for the position-selective intramolecular
C–H amination of aliphatic groups (Hofmann–Löffler reaction) are reported employing …