Journey describing applications of oxone in synthetic chemistry

H Hussain, IR Green, I Ahmed - Chemical reviews, 2013 - ACS Publications
The existence of a peroxygen acid of sulfur was recognized nearly one and half centuries
ago, 1, 2 but it was not until 1898 that Caro 3 demonstrated the existence of two such acids …

Bromide oxidation: A safe strategy for electrophilic brominations

R Van Kerrebroeck, T Horsten… - European Journal of …, 2022 - Wiley Online Library
Bromination of organic substances is still an important reaction in modern synthetic
chemistry. In view of the increasing demand for sustainable synthetic chemistry, oxidative …

Scope and selectivity in palladium-catalyzed directed C–H bond halogenation reactions

D Kalyani, AR Dick, WQ Anani, MS Sanford - Tetrahedron, 2006 - Elsevier
Palladium-catalyzed ligand directed C–H activation/halogenation reactions have been
extensively explored. Both the nature of the directing group and the substitution pattern on …

Oxidative Dearomative Coupling of Electron-Deficient Arenols Using Hypohalite Catalysis

T Kato, N Sahara, S Akagawa, M Uyanik… - Organic …, 2024 - ACS Publications
We developed performant in situ hypohalite, especially hypobromite, catalysis for the
oxidative dearomatization of low-reactivity electron-deficient arenols. The reaction scope …

An environmentally friendly protocol for oxidative halocyclization of tryptamine and tryptophol derivatives

J Xu, R Tong - Green Chemistry, 2017 - pubs.rsc.org
An environmentally friendly and efficient protocol (KX/oxone) for oxidative halocyclization of
tryptamine/tryptophol derivatives was developed and demonstrated with 28 examples and …

Visible Light-Induced Oxidative Chlorination of Alkyl sp3 C–H Bonds with NaCl/Oxone at Room Temperature

M Zhao, W Lu - Organic letters, 2017 - ACS Publications
A visible light-induced monochlorination of cyclohexane with sodium chloride (5: 1) has
been successfully accomplished to afford chlorocyclohexane in excellent yield by using …

Halocarbocyclization versus dihalogenation: substituent directed iodine (III) catalyzed halogenations

M Stodulski, A Goetzinger, SV Kohlhepp… - Chemical …, 2014 - pubs.rsc.org
The nucleophilicity of the substituents in iodobenzene pre-catalysts have a huge impact on
product selectivity in iodine (III) triggered halogenations, steering the reactivity from solely …

A solvent-free catalytic protocol for the Achmatowicz rearrangement

G Zhao, R Tong - Green Chemistry, 2019 - pubs.rsc.org
Reported here is the development of an environmentally friendly catalytic (KBr/oxone) and
solvent-free protocol for the Achmatowicz rearrangement (AchR). Different from all previous …

(Diacetoxyiodo) benzene-lithium bromide as a convenient electrophilic Br+ source

DC Braddock, G Cansell, SA Hermitage - Synlett, 2004 - thieme-connect.com
A mild and versatile procedure for the bromination of olefins and activated arenes by in situ
generation of 'Br+'using (diacetoxyiodo) benzene and lithium bromide is presented. The …

PhI (OAc) 2/NaX-mediated halogenation providing access to valuable synthons 3-haloindole derivatives

V Himabindu, SP Parvathaneni, VJ Rao - New Journal of Chemistry, 2018 - pubs.rsc.org
This paper describes a mild phenyliodine diacetate mediated method for selective
chlorination, bromination, and iodination of indole C–H bonds using sodium halide as a …