Cinnamoylphenethylamine 1H-NMR chemical shifts: a concise reference for ubiquitous compounds.

Nat Prod Commun

Department of Chemistry, University of Copenhagen, Universitetsparken 5, DK-2100, Denmark.

Published: August 2010

1H-NMR data of 25 cinnamoylphenethylamine derivates were recorded and compared in order to assign signals unequivocally without additional spectroscopic data. The spectra provide a key for the rapid identification of these ubiquitous natural products. The compounds isomerize rapidly in UV light, producing a characteristic upfield shift of the olefinic protons consistent with distorted planarity of the cis cinnamate, and this requires special attention during preparative work.

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