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Preparation of iodonium ylides: probing the fluorination of 1,3-dicarbonyl compounds with a fluoroiodane

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journal contribution
posted on 2015-01-27, 12:30 authored by Gemma C. Geary, Eric G. Hope, Kuldip Singh, Alison M. Stuart
The isolation of iodonium ylide 8, from the reaction of fluoroiodane 1 with ethyl 3-oxo-3-phenylpropanoate 5 in the presence of potassium fluoride, provides strong evidence that 1,3-dicarbonyl compounds undergo an addition reaction with fluoroiodane 1 to form an iodonium intermediate which can be deprotonated to generate an iodonium ylide. In the presence of TREAT-HF, however, the iodonium intermediate reacts to form the 2-fluoro-1,3-dicarbonyl product and we propose that fluoroiodane 1 simulates electrophilic fluorination via an addition/substitution mechanism. Further evidence to support this mechanism was obtained by successfully reacting the isolated iodonium ylide 8 with TREAT-HF, hydrochloric acid, acetic acid and p-toluenesulfonic acid to form the 2-fluoro-, 2-chloro-, 2-acetyl- and 2-tosyl-1,3-ketoesters respectively.

History

Citation

G. C. Geary, E. G. Hope, K. Singh and A. M. Stuart, RSC Adv., 2015, DOI: 10.1039/C4RA15733H.

Author affiliation

/Organisation/COLLEGE OF SCIENCE AND ENGINEERING/Department of Chemistry

Version

  • AM (Accepted Manuscript)

Published in

G. C. Geary

Publisher

Royal Society of Chemistry

eissn

2046-2069

Copyright date

2014

Available date

2016-01-22

Publisher version

http://pubs.rsc.org/en/Content/ArticleLanding/2015/RA/C4RA15733H#!divAbstract

Language

en

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