ArticleJournal of natural products2021
Toward a Systematic Nomenclature for (Neo)Lignanamides.
Article in Journal of natural products, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed.
- Natural Strategies to Preserve Alcohol-Free Beer: Phenolamide Dimers with Anti-Yeast Potential.Journal of agricultural and food chemistry · 2026Article
- Comprehensive review on cannabis seed phenolic compounds from extraction to functional applications.Journal of cannabis research · 2026Review
- Comment on "Three New Dimers and Two Monomers of Phenolic Amides from the Fruits ofJournal of agricultural and food chemistry · 2024Article
- Biomimetic Enzymatic Oxidative Coupling of Barley Phenolamides: Hydroxycinnamoylagmatines.Journal of agricultural and food chemistry · 2022Article
- Facile Amidation of Non-Protected Hydroxycinnamic Acids for the Synthesis of Natural Phenol Amides.Molecules (Basel, Switzerland) · 2022Article
- Defense mechanisms involving secondary metabolism in the grass family.Journal of pesticide science · 2021Article
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Authors and funding
10 authors.
Funding
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Abstract
Phenylalkenoic acid amides, often referred to as phenol amides or hydroxycinnamic acid amides, are bioactive phytochemicals, whose bioactivity can be enhanced by coupling to form dimers or oligomers. Phenylalkenoic acid amides consist of a (hydroxy)cinnamic acid derivative (i.e., the phenylalkenoic acid subunit) linked to an amine-containing compound (i.e., the amine subunit) via an amide bond. The phenylalkenoic acid moiety can undergo oxidative coupling, either catalyzed by oxidative enzymes or due to autoxidation, which leads to the formation of (neo)lignanamides. Dimers described in the literature are often named after the species in which the compound was first discovered; however, the naming of these compounds lacks a systematic approach. We propose a new nomenclature, inspired by the existing system used for hydroxycinnamic acid dimers and lignin. In the proposed systematic nomenclature for (neo)lignanamides, compound names will be composed of three-letter codes and prefixes denoting the subunits, and numbers that indicate the carbon atoms involved in the linkage between the monomeric precursors. The proposed nomenclature is consistent, future-proof, and systematic.
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