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Please use this identifier to cite or link to this item: https://dspace.lboro.ac.uk/2134/18334

Title: Organocatalytic asymmetric domino Michael-Henry reaction for the synthesis of substituted bicyclo[3.2.1]octan-2-ones
Authors: Tsakos, Michail
Elsegood, Mark R.J.
Kokotos, Christoforos G
Issue Date: 2013
Publisher: © Royal Society of Chemistry
Citation: TSAKOS, M., ELSEGOOD, M.R.J. and KOKOTOS, C.G., 2013. Organocatalytic asymmetric domino Michael-Henry reaction for the synthesis of substituted bicyclo[3.2.1]octan-2-ones. Chemical Communications, 49 (22), pp.2219-2221
Abstract: The first organocatalytic asymmetric reaction between 1,4-cyclohexanedione and nitroalkenes have been studied, affording bicyclo[3.2.1]octane derivatives containing four continuous stereogenic centres. The products were obtained through a domino Michael-Henry process as a single diastereoisomer with excellent enantioselectivities.
Description: This paper was submitted for publication in the journal "Chemical Communications" and the definitive version can be found at: http://dx.doi.org/10.1039/c3cc39165e
Version: Accepted for publication
DOI: 10.1039/c3cc39165e
URI: https://dspace.lboro.ac.uk/2134/18334
Publisher Link: http://dx.doi.org/10.1039/c3cc39165e
ISSN: 1359-7345
Appears in Collections:Published Articles (Chemistry)

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