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(±)-Paeoveitol, a Pair of New Norditerpene Enantiomers from Paeonia veitchii
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/hlca.200590007openalex-snapshot
Three Novel 24,30-Dinortriterpenoids, Paeonenoides A-C, fromPaeonia veitchii
inferredcites →https://doi.org/10.1016/0031-9422(95)00526-9openalex-snapshot
Monoterpene glycosides from Paeonia suffruticosa
inferredcites →https://doi.org/10.1016/j.jep.2008.07.008openalex-snapshot
Antidepressant-like effect of peony glycosides in mice
inferredcites →https://doi.org/10.1016/j.phytochem.2008.02.016openalex-snapshot
Monoterpene glycosides from Paeonia hybrida
inferredcites →https://doi.org/10.1016/s0006-3223(02)01643-8openalex-snapshot
Is there a role for 5-HT1A agonists in the treatment of depression?
inferredcites →https://doi.org/10.1016/s0031-9422(97)00683-3openalex-snapshot
A monoterpene glucoside from Paeonia peregrina roots
inferredcites →https://doi.org/10.1016/s0040-4020(01)88953-5openalex-snapshot
Chemical studies on the oriental plant drugs—XXXIII
inferredcites →https://doi.org/10.1021/ja064550uopenalex-snapshot
The Boat-Shaped Polyketide Resistoflavin Results from Re-Facial Central Hydroxylation of the Discoid Metabolite Resistomycin
inferredcites →https://doi.org/10.1021/np9001898openalex-snapshot
Monoterpenes from Paeonia albiflora and Their Inhibitory Activity on Nitric Oxide Production by Lipopolysaccharide-Activated Microglia
inferredcites →https://doi.org/10.1055/s-2006-957692openalex-snapshot
Antihyperglycemic Effects of Paeoniflorin and 8-Debenzoylpaeoniflorin, Glucosides from the Root ofPaeonia lactiflora
inferredcites →https://doi.org/10.1248/cpb.33.3838openalex-snapshot
Metabolism of paeoniflorin and related compounds by human intestinal bacteria.
inferredcites →https://doi.org/10.2515/therapie:2005065openalex-snapshot
Serotonin 5-HT2C Receptors as a Target for the Treatment of Depressive and Anxious States: Focus on Novel Therapeutic Strategies
inferredcites →https://doi.org/10.3389/fphar.2011.00010openalex-snapshot
Anti-Inflammatory and Immunomodulatory Effects of Paeonia Lactiflora Pall., a Traditional Chinese Herbal Medicine
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4666804openalex-extracted
Inverse Electron Demand Diels-Alder Reaction in Total Synthesis of Bioactive Natural Products
inferred← citeshttps://doi.org/10.1002/chin.201426195openalex-snapshot
ChemInform Abstract: (.+‐.)‐Paeoveitol, a Pair of New Norditerpene Enantiomers from Paeonia veitchii.
inferred← citeshttps://doi.org/10.1002/cmdc.202100782openalex-snapshot
Synthesis of Dihydrobenzofuro[3,2‐b]chromenes as Potential 3CLpro Inhibitors of SARS‐CoV‐2: A Molecular Docking and Molecular Dynamics Study
inferred← citeshttps://doi.org/10.1002/ejoc.201701481openalex-snapshot
Stereoselective Intramolecular Dearomatizative [4+2] Cycloaddition of Linked Ethynylnaphthol–Benzofuran Systems
inferred← citeshttps://doi.org/10.1007/978-3-032-09901-3_1openalex-snapshot
The Diels–Alder Reaction as a Key Step in Natural Product Synthesis
inferred← citeshttps://doi.org/10.1007/978-981-99-7329-3_3openalex-snapshot
Classification of Diverse Novel Diterpenoids
inferred← citeshttps://doi.org/10.1007/s00044-022-02973-0openalex-snapshot
Synthesis and biological evaluation of (+)-paeoveitol derivatives as novel antidepressants
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.104783openalex-snapshot
Paeonone A, a novel nonanortriterpenoid from the roots of Paeonia lactiflora
inferred← citeshttps://doi.org/10.1016/j.fitote.2015.07.015openalex-snapshot
Paeoveitols A–E from Paeonia veitchii
inferred← citeshttps://doi.org/10.1016/j.fitote.2025.106638openalex-snapshot
Cabreuvanols A-C, three new cassane-derived diterpenes from Myrocarpus frondosus and their anti-inflammatory effects
inferred← citeshttps://doi.org/10.1016/j.jep.2020.113708openalex-snapshot
Genus Paeonia: A comprehensive review on traditional uses, phytochemistry, pharmacological activities, clinical application, and toxicology
inferred← citeshttps://doi.org/10.1016/j.tchem.2024.100066openalex-snapshot
Inverse electron demand Diels-Alder reaction in total synthesis of bioactive natural products
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.03.037openalex-snapshot
A vicarious, one-pot synthesis of benzo- and naphthofurans: Applications to the syntheses of stereumene B and paeoveitols
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00087openalex-snapshot
Structures and Biological Evaluation of Monoterpenoid Glycosides from the Roots of Paeonia lactiflora
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b01736openalex-snapshot
A Total Synthesis of Paeoveitol
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02228openalex-snapshot
Biomimetic Total Synthesis of Paeoveitol
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b03801openalex-snapshot
Catalytic Asymmetric Total Synthesis of (+)- and (−)-Paeoveitol via a Hetero-Diels–Alder Reaction
inferred← citeshttps://doi.org/10.1039/c4ob00228hopenalex-snapshot
Water-promoted ortho-selective monohydroxymethylation of phenols in the NaBO 2 system
inferred← citeshttps://doi.org/10.1039/d0cs01124jopenalex-snapshot
Recent applications of asymmetric organocatalytic annulation reactions in natural product synthesis
inferred← citeshttps://doi.org/10.1039/d2md00156jopenalex-snapshot
Synthesis and biological evaluation of paeoveitol D derivatives as new melatonin receptor agonists with antidepressant activities
inferred← citeshttps://doi.org/10.1051/e3sconf/202124503068openalex-snapshot
Applications of chiral spirocyclic phosphoric acid in the synthesis of natural products
inferred← citeshttps://doi.org/10.1055/a-1532-4763openalex-snapshot
Recent Applications of the Diels–Alder Reaction in the Synthesis of Natural Products (2017–2020)
inferred← citeshttps://doi.org/10.1080/00397911.2022.2119414openalex-snapshot
A scalable and diversity-oriented synthesis of (±)-paeoveitols
inferred← citeshttps://doi.org/10.1080/10286020.2014.922553openalex-snapshot
Two new sesquiterpenoid glycosides from Nicotiana tabacum
inferred← citeshttps://doi.org/10.3390/molecules27041279openalex-snapshot
Natural Enantiomers: Occurrence, Biogenesis and Biological Properties
inferred← citeshttps://doi.org/10.3390/molecules29010060openalex-snapshot
A Comprehensive Review of the Classification, Sources, Phytochemistry, and Pharmacology of Norditerpenes
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