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肉桂酰苯乙胺的1H-NMR化学位移:常见化合物的简明参考。

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

作者信息

Pedersen Hans A, Steffensen Stine K, Christophersen Carsten

机构信息

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

出版信息

Nat Prod Commun. 2010 Aug;5(8):1259-62.

Abstract

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.

摘要

记录并比较了25种肉桂酰苯乙胺衍生物的1H-NMR数据,以便在无需额外光谱数据的情况下明确归属信号。这些光谱为快速鉴定这些普遍存在的天然产物提供了关键依据。这些化合物在紫外光下会迅速异构化,导致烯烃质子产生特征性的高场位移,这与顺式肉桂酸酯平面性扭曲一致,在制备工作过程中需要特别注意这一点。

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