Stabilization of Ethynyl-Substituted Aryl-λ3-Iodanes by Tethered N-Heterocylces

22 February 2022, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

A systematic investigation of ethynyl N-heterocycle-substituted-λ3-iodanes (ENHIs) is presented. In a straightforward one-pot synthesis these novel reagents can be obtained in high yields bearing a variety of N-heterocycles. Their reactivity as electrophilic alkyne group transfer reagents was benchmarked in well-established as well as novel inter- and intramolecular group transfer reactions and compared to literature-known ethynyl benziodoxolones.

Keywords

Hypervalent Iodine
Heterocycles
Iodonium Salts
One-Pot Reactions
Group Transfer Reactions
Iodane

Supplementary materials

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Title
Stabilization of Ethynyl-Substituted Aryl-λ3-Iodanes by Tethered N-Heterocylces
Description
This article describes novel EBX-derived N-heterocycle-stabilized alkynyl-iodonium salts and -iodanes.
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