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Chromatographic and Mass Spectrometric Characterization of Phenanthrenes Supported by Quantum Chemical Calculations and Their Quantitation in Herb

https://doi.org/10.2139/ssrn.4756165
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Positive and negative ions of the amino acid histidine formed in low‐energy electron collisions
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Re‐examination of the anion derivatives of isoflavones by radical fragmentation in negative electrospray ionization tandem mass spectrometry: experimental and computational studies
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Antibacterial screening of Juncaceae species native to the Carpathian Basin against resistant strains and LC-MS investigation of phenanthrenes responsible for the effect
inferredcites →https://doi.org/10.1016/j.fitote.2018.09.007openalex-extracted
Three new phenanthrenes with antimicrobial activities from the aerial parts of Juncus effusus
inferredcites →https://doi.org/10.1016/j.foodchem.2012.05.074openalex-extracted
Synthesis and antioxidant activity of hydroxylated phenanthrenes as cis-restricted resveratrol analogues
inferredcites →https://doi.org/10.1016/j.phytochem.2007.12.005openalex-extracted
Natural phenanthrenes and their biological activity
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Focusing on the 5F-MDMB-PICA, 4F-MDMB-BICA synthetic cannabinoids and their primary metabolites in analytical and pharmacological aspects
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Bond Dissociation Energies of Metallo-supramolecular Building Blocks: Insight from Fragmentation of Selectively Self-Assembled Heterometallic Metallo-supramolecular Aggregates
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Gerardiins A–L and Structurally Related Phenanthrenes from the Halophyte Plant Juncus gerardii and Their Cytotoxicity against Triple-Negative Breast Cancer Cells
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Phenanthrenes fromJuncus inflexuswith Antimicrobial Activity against Methicillin-ResistantStaphylococcus aureus
inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00619openalex-extracted
Phenanthrenes: A Promising Group of Plant Secondary Metabolites
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Comparative mechanisms of reaction of K-region and non-K-region arene oxides of phenanthrene
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Theoretical Study of X−H Bond Energetics (X = C, N, O, S): Application to Substituent Effects, Gas Phase Acidities, and Redox Potentials
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Prediction of organic homolytic bond dissociation enthalpies at near chemical accuracy with sub-second computational cost
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Self-Consistent Molecular-Orbital Methods. IX. An Extended Gaussian-Type Basis for Molecular-Orbital Studies of Organic Molecules
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MetFrag relaunched: incorporating strategies beyond in silico fragmentation
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Phenanthrene Dimers: Promising Source of Biologically Active Molecules
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Phenanthrenes from Juncus Compressus Jacq. with Promising Antiproliferative and Anti-HSV-2 Activities
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A Mass Spectrometry-Based Approach for Characterization of Red, Blue, and Purple Natural Dyes
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