Source:http://linkedlifedata.com/resource/pubmed/id/20839631
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
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pubmed:dateCreated |
2010-9-15
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pubmed:abstractText |
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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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
1934-578X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
5
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1259-62
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pubmed:meshHeading | |
pubmed:year |
2010
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pubmed:articleTitle |
Cinnamoylphenethylamine 1H-NMR chemical shifts: a concise reference for ubiquitous compounds.
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pubmed:affiliation |
Department of Chemistry, University of Copenhagen, Universitetsparken 5, DK-2100, Denmark.
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pubmed:publicationType |
Journal Article
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