Chiral hypervalent iodines: active players in asymmetric synthesis

A Parra - Chemical Reviews, 2019 - ACS Publications
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) …

Chemistry of polyvalent iodine

VV Zhdankin, PJ Stang - Chemical reviews, 2008 - ACS Publications
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 …

Hypervalent iodine (III) fluorinations of alkenes and diazo compounds: new opportunities in fluorination chemistry

SV Kohlhepp, T Gulder - Chemical Society Reviews, 2016 - pubs.rsc.org
The fluorination of organic molecules is a rapidly evolving and exciting field in synthesis,
which still poses huge challenges despite the advances made in the past decades …

Hypervalent iodine chemistry in synthesis: Scope and new directions

T Wirth - Angewandte Chemie International Edition, 2005 - Wiley Online Library
The impressive development of hypervalent iodine chemistry in recent years is reflected by
the number of publications in this area. Although the synthesis of the first hypervalent iodine …

Vicinal difunctionalization of alkenes with iodine (III) reagents and catalysts

RM Romero, TH Wöste, K Muñiz - 2014 - recercat.cat
Hypervalent iodine (III) reagents have been known for over a century, and their reaction
profile is still actively investigated. Recent years have seen impressive improvements in the …

Unlocking the Friedel-Crafts arylation of primary aliphatic alcohols and epoxides driven by hexafluoroisopropanol

S Zhang, M Vayer, F Noel, VD Vuković, A Golushko… - Chem, 2021 - cell.com
Alcohols and epoxides are arguably ideal electrophiles for the Friedel-Crafts alkylation,
since they are widely available, require no pre-activation, and produce no stoichiometric …

Structurally defined molecular hypervalent iodine catalysts for intermolecular enantioselective reactions

S Haubenreisser, TH Wöste, C Martínez… - Angewandte Chemie …, 2016 - Wiley Online Library
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 …

Hypervalent iodine reactions utilized in carbon–carbon bond formations

IFD Hyatt, L Dave, N David, K Kaur… - Organic & …, 2019 - pubs.rsc.org
Advances in hypervalent iodine chemistry have put the field on the precipice of a second
golden age; the first being pioneered in the 1990s. During that period, C–C bond forming …

[PDF][PDF] Hypervalent iodine (III) reagents in organic synthesis.

VV Zhdankin - ARKIVOC: Online Journal of Organic Chemistry, 2009 - Citeseer
This review summarizes the chemistry of hypervalent iodine (III) compounds with emphasis
of their synthetic applications. The preparation and reactions of (difluoroiodo) …

Mild Silver‐Mediated Geminal Difluorination of Styrenes Using an Air‐and Moisture‐Stable Fluoroiodane Reagent

NO Ilchenko, BOA Tasch, KJ Szabó - Angewandte Chemie, 2014 - Wiley Online Library
An air‐and moisture‐stable fluoroiodane in the presence of AgBF4 is suitable for selective
geminal difluorination of styrenes under mild reaction conditions. One of the C F bonds is …