Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/31501
Title: Preparation of iodonium ylides: probing the fluorination of 1,3-dicarbonyl compounds with a fluoroiodane
Authors: Geary, Gemma C.
Hope, Eric G.
Singh, Kuldip
Stuart, Alison M.
First Published: 22-Jan-2015
Publisher: Royal Society of Chemistry
Citation: G. C. Geary, E. G. Hope, K. Singh and A. M. Stuart, RSC Adv., 2015, DOI: 10.1039/C4RA15733H.
Abstract: 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.
DOI Link: 10.1039/c4ra15733h
eISSN: 2046-2069
Links: http://pubs.rsc.org/en/Content/ArticleLanding/2015/RA/C4RA15733H#!divAbstract
http://hdl.handle.net/2381/31501
Version: Post-print
Status: Peer-reviewed
Type: Journal Article
Rights: Copyright the author 2014. Version of record: http://pubs.rsc.org/en/Content/ArticleLanding/2015/RA/C4RA15733H
Appears in Collections:Published Articles, Dept. of Chemistry

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