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A valuable upgrade to the portfolio of cycloaddition reactions

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CycloANIEtext1.pdf (441.4Kb)
Date
09/06/2016
Author
Walton, John C.
Keywords
Carbocycles
Copper
Cyclotrimerization
Radicals
Synthetic methods
QD Chemistry
NDAS
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Abstract
Recently Antonchick and Manna described a unique annulation that knits together three acetophenones to construct cyclopropanes. The cascade is mediated by organo-copper and free radical species and amounts to the first known [1+1+1] cyclotrimerization. It works well for ketones having electron-deficient or electron-rich substituents in their aryl rings.
Citation
Walton , J C 2016 , ' A valuable upgrade to the portfolio of cycloaddition reactions ' , Angewandte Chemie International Edition , vol. 55 , no. 25 , pp. 7034-7036 . https://doi.org/10.1002/anie.201602891
Publication
Angewandte Chemie International Edition
Status
Peer reviewed
DOI
https://doi.org/10.1002/anie.201602891
ISSN
1521-3773
Type
Journal article
Rights
© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. This work is made available online in accordance with the publisher’s policies. This is the author created, accepted version manuscript following peer review and may differ slightly from the final published version. The final published version of this work is available at https://dx.doi.org/10.1002/anie.201602891
Description
The author thanks EaStCHEM for financial support.
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  • University of St Andrews Research
URI
http://hdl.handle.net/10023/10696

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