Asymmetric organocatalytic oxidations have been witnessed to an impressive development
in the last years thanks to the establishment of important chiral hypervalent iodines (III/V) …

The implementation of chiral iodine catalysis has tremendously been developed in the field
of asymmetric synthesis over the past decade. It enables the stereoselective creation of C–O …

Chiral hypervalent iodine chemistry has been steadily increasing in importance in recent
years. This review catalogues enantioselective transformations triggered by chiral …

Molecular structures of the most prominent chiral non‐racemic hypervalent iodine (III)
reagents to date have been elucidated for the first time. The formation of a chirally induced …

In this review are compiled the different possible transformations using environmentally
benign chiral hypervalent iodine reagents and catalysts. Herein is presented an overview of …

Hypervalent iodine reagents are unusually effective promoters of transformations that would
be difficult, perhaps impossible, to accomplish otherwise. Low toxicity, a favorable safety …

Chiral aryliodine (III) reagents have provided an advanced concept for enantioselective
synthesis and catalysis. With the advent of chiral iodine (I/III) catalysis, many different …

The enantioselective oxidative dearomatization of phenols and their analogues is a key
reaction for the synthesis of several natural products.[1] Conventionally, enantioselective …

Conspectus The quest for the development of new protocols that provide general conditions
for oxidative carbon–nitrogen bond formation has grown over recent years. Within this …

A remarkable growth in hypervalent iodine‐mediated oxidative transformations as
stoichiometric reagents as well as catalysts has been well‐documented due to their …