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Beilstein Journal of Organic Chemistry
Article . 2018 . Peer-reviewed
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Beilstein Journal of Organic Chemistry
Article
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Imide arylation with aryl(TMP)iodonium tosylates

Authors: Souradeep Basu; Alexander H Sandtorv; David R Stuart;

Imide arylation with aryl(TMP)iodonium tosylates

Abstract

Herein, we describe the synthesis of N-aryl phthalimides by metal-free coupling of potassium phthalimide with unsymmetrical aryl(TMP)iodonium tosylate salts. The aryl transfer from the iodonium moiety occurs under electronic control with the electron-rich trimethoxyphenyl group acting as a competent dummy ligand. The yields of N-aryl phthalimides are moderate to high and the coupling reaction is compatible with electron-deficient and sterically encumbered aryl groups.

Related Organizations
Keywords

hypercoordinate iodine, metal-free, QD241-441, Letter, C–N coupling, diaryliodonium, Science, Q, Organic chemistry, arylation

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    Top 10%
    influence
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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
26
Top 10%
Average
Top 10%
Green
Published in a Diamond OA journal
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