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Mollanol A, a Diterpenoid with a New C-Nor-D-homograyanane Skeleton from the Fruits of Rhododendron molle
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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/cbdv.201000188openalex-snapshot
Lyonin A, a New 9,10‐Secograyanotoxin from Lyonia ovalifolia
inferredcites →https://doi.org/10.1007/s11101-013-9299-zopenalex-snapshot
Grayanoids from the Ericaceae family: structures, biological activities and mechanism of action
inferredcites →https://doi.org/10.1016/0031-9422(91)85015-ropenalex-snapshot
Grayanoid diterpene insect antifeedants and insecticides from Rhododendron molle
inferredcites →https://doi.org/10.1016/j.cell.2008.07.021openalex-snapshot
XBP1 Links ER Stress to Intestinal Inflammation and Confers Genetic Risk for Human Inflammatory Bowel Disease
inferredcites →https://doi.org/10.1016/s0040-4039(01)82168-7openalex-snapshot
Stereostructure of grayanol A and B, diterpenoids of leucothoe grayana
inferredcites →https://doi.org/10.1016/s0040-4039(01)98631-9openalex-snapshot
Crystal and molecular structure of grayanotoxin - I, C22H36O7
inferredcites →https://doi.org/10.1021/ja00197a050openalex-snapshot
Kalmanol, a pharmacologically active diterpenoid with a new ring skeleton from Kalmia angustifolia L
inferredcites →https://doi.org/10.1021/ja9533454openalex-snapshot
Studies Directed to the Synthesis of the Unusual Cardiotoxic Agent Kalmanol. Enantioselective Construction of the Advanced Tetracyclic 7-Oxy-5,6-dideoxy Congener
inferredcites →https://doi.org/10.1021/np050261sopenalex-snapshot
Iridoid Glycosides and Grayanane Diterpenoids from the Roots of Craibiodendron henryi
inferredcites →https://doi.org/10.1021/np500074qopenalex-snapshot
Diterpenoids from the Flowers of Rhododendron molle
inferredcites →https://doi.org/10.1021/ol1002797openalex-snapshot
Highly Acylated Diterpenoids with a New 3,4-Secograyanane Skeleton from the Flower Buds ofRhododendron molle
inferredcites →https://doi.org/10.1021/ol1007982openalex-snapshot
Novel Polyesterified 3,4-seco-Grayanane Diterpenoids as Antifeedants from Pieris formosa
inferredcites →https://doi.org/10.1021/ol202147ropenalex-snapshot
Determining a Synthetic Approach to Pierisformaside C
inferredcites →https://doi.org/10.1021/ol401254eopenalex-snapshot
Mollolide A, a Diterpenoid with a New 1,10:2,3-Disecograyanane Skeleton from the Roots of Rhododendron molle
inferredcites →https://doi.org/10.1021/ol401292yopenalex-snapshot
Micranthanone A, a New Diterpene with an Unprecedented Carbon Skeleton from Rhododendron micranthum
inferredcites →https://doi.org/10.1074/jbc.m212133200openalex-snapshot
Distinct Sites Regulating Grayanotoxin Binding and Unbinding to D4S6 of Nav1.4 Sodium Channel as Revealed by Improved Estimation of Toxin Sensitivity
inferredcites →https://doi.org/10.1246/cl.1972.783openalex-snapshot
LEUCOTHOL A, AN ANTHRADITERPENOID FROM LEUCOTHOE GRAYANA MAX.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112524zenodo-depositor-declared
Meroterpenoids with diverse structures and anti-inflammatory activities from Rhododendron anthopogonoides
inferred← citeshttps://doi.org/10.1002/chem.201900807openalex-snapshot
Rapid Access to Oxa‐Bridged Bicyclic Skeletons through Gold‐Catalyzed Tandem Rearrangement Reaction
inferred← citeshttps://doi.org/10.1002/chin.201508268openalex-snapshot
ChemInform Abstract: Mollanol A, a Diterpenoid with a New C‐Nor‐D‐homograyanane Skeleton from the Fruits of Rhododendron molle.
inferred← citeshttps://doi.org/10.1002/cjoc.202100077openalex-snapshot
Epoxymicranthols A—N, 5, 9‐Epoxygrayanane Diterpenoids as Potent Analgesics from Rhododendron micranthum
inferred← citeshttps://doi.org/10.1002/cjoc.202400898openalex-snapshot
Total Syntheses of Highly Oxidized Natural Products†
inferred← citeshttps://doi.org/10.1007/978-981-99-7329-3_3openalex-snapshot
Classification of Diverse Novel Diterpenoids
inferred← citeshttps://doi.org/10.1016/b978-0-443-23754-6.00009-4openalex-snapshot
Progress in the study of natural grayanane diterpenoids
inferred← citeshttps://doi.org/10.1016/j.apsb.2019.10.013openalex-snapshot
Antinociceptive grayanane-derived diterpenoids from flowers of Rhododendron molle
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.103794openalex-snapshot
Structurally diverse diterpenoids from Pieris japonica as potent analgesics
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.104870openalex-snapshot
Structurally diverse diterpenoids with eight carbon skeletons from Rhododendron micranthum and their antinociceptive effects
inferred← citeshttps://doi.org/10.1016/j.bioorg.2023.106374openalex-snapshot
Highly oxygenated grayanane diterpenoids with structural diversity from the flowers of Rhododendron dauricum and their analgesic activities
inferred← citeshttps://doi.org/10.1016/j.cclet.2017.02.020openalex-snapshot
Three new dimeric diterpenes from Rhododendron molle
inferred← citeshttps://doi.org/10.1016/j.cclet.2023.109229openalex-snapshot
Strategies for constructing seven-membered rings: Applications in natural product synthesis
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.01.079openalex-snapshot
An overview of grayanane diterpenoids and their biological activities from the Ericaceae family in the last seven years
inferred← citeshttps://doi.org/10.1016/j.fitote.2018.12.007openalex-snapshot
Diverse epoxy grayanane diterpenoids with analgesic activity from the roots of Pieris formosa
inferred← citeshttps://doi.org/10.1016/j.fitote.2024.106017openalex-snapshot
Nivalones C F, four new meroterpenoids from Rhododendron nivale
inferred← citeshttps://doi.org/10.1016/j.fitote.2026.107116openalex-snapshot
Grayanane diterpenoids from Rhododendron molle: Structural diversity, mechanisms of antinociceptive action, and structure-activity relationships
inferred← citeshttps://doi.org/10.1016/j.jep.2022.115581openalex-snapshot
The efficacy and toxicity of grayanoids as analgesics: A systematic review
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113425openalex-snapshot
Unprecedented diterpene skeletons isolated from vascular plants in the last twenty years (2001–2021)
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113545openalex-snapshot
Eudesmane−type sesquiterpenes from the rhizomes of Atractylodes macrocephala and their bioactivities
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113899openalex-snapshot
An updated review of the genus Rhododendron since 2010: Traditional uses, phytochemistry, and pharmacology
inferred← citeshttps://doi.org/10.1016/j.tet.2016.12.060openalex-snapshot
Isopimarane and nor-diterpene glucosides from the twigs and leaves of Lyonia ovalifolia
inferred← citeshttps://doi.org/10.1016/j.tet.2022.132892openalex-snapshot
Analgesic grayanoids from Craibiodendron henryi
inferred← citeshttps://doi.org/10.1016/j.tet.2025.134901openalex-snapshot
Applications of Conia-ene reaction in total synthesis of natural products
inferred← citeshttps://doi.org/10.1016/j.tetlet.2024.155160openalex-snapshot
Five decades of endeavor towards total syntheses of grayanane diterpenoids
inferred← citeshttps://doi.org/10.1021/acs.jafc.7b03461openalex-snapshot
Structural Diversity and Biological Activity of the Genus Pieris Terpenoids
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00456openalex-snapshot
Antinociceptive Grayanoids from the Roots of Rhododendron molle
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00799openalex-snapshot
Anti-inflammatory Grayanane Diterpenoids from the Leaves of Rhododendron molle
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00095openalex-snapshot
Grayanane Diterpenoids from the Leaves of Rhododendron auriculatum and Their Analgesic Activities
inferred← citeshttps://doi.org/10.1021/acs.joc.1c01648openalex-snapshot
Straightforward Stereoselective Synthesis of Seven-Membered Oxa-Bridged Rings through In Situ Generated Cycloheptenol Derivatives
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02800openalex-snapshot
Five Pairs of Meroterpenoid Enantiomers from Rhododendron capitatum
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b02515openalex-snapshot
Two Enantiomeric Pairs of Meroterpenoids from Rhododendron capitatum
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01863openalex-snapshot
Rhodomollanol A, a Highly Oxygenated Diterpenoid with a 5/7/5/5 Tetracyclic Carbon Skeleton from the Leaves of Rhododendron molle
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b02633openalex-snapshot
Rhodomollacetals A–C, PTP1B Inhibitory Diterpenoids with a 2,3:5,6-Di-seco-grayanane Skeleton from the Leaves of Rhododendron molle
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b00606openalex-snapshot
Mollebenzylanols A and B, Highly Modified and Functionalized Diterpenoids with a 9-Benzyl-8,10-dioxatricyclo[5.2.1.01,5]decane Core from Rhododendron molle
inferred← citeshttps://doi.org/10.1021/jacs.6c03596openalex-snapshot
Enantioselective Total Syntheses of Grayanoid (−)-Mollfoliagein A and (−)-Rhodomollein XXV
inferred← citeshttps://doi.org/10.1038/s41598-017-06320-xopenalex-snapshot
Rhodoterpenoids A‒C, Three New Rearranged Triterpenoids from Rhododendron latoucheae by HPLC‒MS‒SPE‒NMR
inferred← citeshttps://doi.org/10.1038/srep36752openalex-snapshot
Rhodomollins A and B, two Diterpenoids with an Unprecedented Backbone from the Fruits of Rhododendron molle
inferred← citeshttps://doi.org/10.1039/c5np00087dopenalex-snapshot
Diterpenoids of terrestrial origin
inferred← citeshttps://doi.org/10.1039/c6np00059bopenalex-snapshot
Diterpenoids of terrestrial origin
inferred← citeshttps://doi.org/10.1039/c7ra08635kopenalex-snapshot
Biological and chemical guided isolation of 3,4-secograyanane diterpenoids from the roots of Pieris formosa
inferred← citeshttps://doi.org/10.1039/d0ob00160kopenalex-snapshot
Toward the total synthesis of grayanane diterpene mollanol A by a Prins [3 + 2] strategy
inferred← citeshttps://doi.org/10.1039/d5ra09257dopenalex-snapshot
Total synthesis of natural products facilitated by prins reaction: a review
inferred← citeshttps://doi.org/10.1055/a-2103-9925openalex-snapshot
The Total Synthesis of Mollanol A by a Convergent Strategy
inferred← citeshttps://doi.org/10.13005/bbra/2939openalex-snapshot
Research Progress on the Identification and Pharmacological Activity of the Active Components of the Rhododendron Species
inferred← citeshttps://doi.org/10.3184/003685016x14720691270831openalex-snapshot
From ‘Mad Honey’ to Hypotensive Agents, the Grayanoid Diterpenes
inferred← citeshttps://doi.org/10.3389/fphar.2026.1772696openalex-snapshot
A review of Rhododendron molle: traditional uses, clinical applications, phytochemistry, pharmacology, toxicology, pharmacokinetics and quality control
inferred← citeshttps://doi.org/10.3390/molecules22091431openalex-snapshot
New Antifeedant Grayanane Diterpenoids from the Flowers of Pieris formosa
inferred← citeshttps://doi.org/10.70675/4bf5e5f4zeddbz4ea7z8eeaze6b7153e69deopenalex-snapshot
Synthèse totale collective de terpénoïdes complexes, vers les grayananes et les kalmanes
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