Starting from the early 1990s, the chemistry of polyvalent iodine organic compounds has
experienced an explosive development. This surging interest in iodine compounds is mainly …

Bromination of organic substances is still an important reaction in modern synthetic
chemistry. In view of the increasing demand for sustainable synthetic chemistry, oxidative …

High-Yielding Oxidation of β-Hydroxyketones to β-Diketones Using o-Iodoxybenzoic Acid | The
Journal of Organic Chemistry ACS ACS Publications C&EN CAS Find my institution Log In The …

A mild and rapid (diacetoxyiodo) benzene-mediated formal electrophilic α-azidation of 1, 3-
dicarbonyl compounds using commercially available Bu4NN3 as the azide source is …

This communication describes the first proof of concept for an asymmetric α-cyanation of β-
ketoesters using a hypervalent iodine-based electrophilic cyanide-transfer reagent. A series …

The reaction of β-dicarbonyl compounds (β-ketoesters and β-diketones) with 0.34 molequiv
of trichloro-and tribromoisocyanuric acids produced regioselectively the corresponding α …

A versatile protocol for the synthesis of disubstituted 3-phenylimidazo [1, 2-a] pyridines by
coupling 2-aminopyridine with phenylacetophenones, phenylacetones, or β-tetralone has …

An electrochemical strategy to the assembly of tricyclic spiro dihydrofuran scaffold via the
reaction of aryl aldehyde and dimedone has been developed successfully. This protocol has …

The chemistry of hypervalent iodine compounds has been experiencing considerable
attention of organic chemists during the past few years. Hypervalent iodine reagents have …

In this work, we present a solvent‐controlled regioselective method for α‐monobromination,
dibromination or imidation of 1, 3‐diketones with N‐bromosuccinimide under simple …