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dc.contributor.authorGeary, Gemma C.-
dc.contributor.authorHope, Eric G.-
dc.contributor.authorStuart, Alison M.-
dc.identifier.citationAngewandte Chemie International Edition, 2015 (Early View, In press)en
dc.descriptionThe file associated with this record is under a 12-month embargo from publication in accordance with the publisher Copyright transfer agreement, available at The full text may be available through the publisher links provided above.en
dc.description.abstractA new class of fluorinated lactones was prepared by the intramolecular fluorocyclizations of unsaturated carboxylic acids by using the stable fluoroiodane reagent in combination with AgBF4 . This unique reaction incorporates a cyclization, an aryl migration, and a fluorination all in one step. The fluoroiodane reagent, prepared easily from fluoride, can also be used without a metal catalyst to give moderate yields within just 1 hour, thus demonstrating that it is a suitable reagent for developing new (18) F-labelled radiotracers for PET imaging.en
dc.publisherWiley-VCH Verlagen
dc.rightsCopyright © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. This is the accepted version of the following article: Geary, G. C., Hope, E. G. and Stuart, A. M. (2015), Intramolecular Fluorocyclizations of Unsaturated Carboxylic Acids with a Stable Hypervalent Fluoroiodane Reagent. Angew. Chem. Int. Ed.. doi:10.1002/anie.201507790, which has been published in final form at doi: 10.1002/anie.201507790en
dc.subjecthypervalent compoundsen
dc.titleIntramolecular Fluorocyclizations of Unsaturated Carboxylic Acids with a Stable Hypervalent Fluoroiodane Reagenten
dc.typeJournal Articleen
dc.type.subtypeJOURNAL ARTICLE-
pubs.organisational-group/Organisation/COLLEGE OF SCIENCE AND ENGINEERINGen
pubs.organisational-group/Organisation/COLLEGE OF SCIENCE AND ENGINEERING/Department of Chemistryen
Appears in Collections:Published Articles, Dept. of Chemistry

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