The preparation, structure, and chemistry of hypervalent iodine compounds are reviewed
with emphasis on their synthetic application. Compounds of iodine possess reactivity similar …

The chemistry of hypervalent iodine reagents has now become quite valuable due to the
reactivity of these compounds under mild reaction conditions and their resemblance in …

We describe an eco-friendly, practical and operationally simple procedure for the bis
(methoxypropyl) ether-promoted oxidation of aromatic alcohols into aromatic carboxylic …

Oxidative cleavage of a variety of olefins to the corresponding ketones/carboxylic acids is
shown to occur in a facile manner with 3, 4, 5, 6-tetramethyl-2-iodobenzoic acid (TetMe …

Visible light-mediated facile synthesis of heteroarenes, namely, isoquinolines,
benzothiazoles, and quinazolines, is demonstrated by employing isocyanides and …

Hypervalent iodine (III and V) compounds exhibit positional isomerization through
pseudorotation or twisting; the latter have been invoked for the stability as well as the …

This work demonstrates the preparation of zinc cobalt oxide materials (ZCO-1, ZCO-2, and
ZCO-3) via thermal annealing of novel zinc cobalt acetate hydroxide precursors prepared in …

Several reactions mended by hypervalent iodine reagents have been developed in aqueous
media recently. The evolution of reactions using hypervalent iodine reagents in aqueous …

IBX is an indispensable reagent in contemporary organic oxidation chemistry, despite its
explosive and insoluble attributes. The latter drawbacks can be overcome if a more reactive …

A variety of olefins is shown to be cleaved oxidatively to the corresponding acids with oxone
as the reagent. The simple methodology that works well for a range of alkenes, ie, styrenes …