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Kalmanol, a pharmacologically active diterpenoid with a new ring skeleton from Kalmia angustifolia L

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inferred← citeshttps://doi.org/10.2139/ssrn.4526894openalex-extracted
Radical Induced Synthesis of Bicyclo[3.3.0]Octane Via Photochemical Irradiation
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Synthetic Studies to exo‐Ring‐Junction based Fused 5/5/n‐Tricyclic Systems: Access to A, B, C‐Ring System of Longeracinphyllin A, Himalenine D, and Daphnipaxiamine A.
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Total Synthesis of (+)‐Kalmanol
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Convergent Total Synthesis of Kalmanol
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Total Synthesis of (+)‐Kalmanol
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Convergent Total Synthesis of Kalmanol
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Pierisformotoxins A – D, Polyesterified Grayanane Diterpenoids from Pieris formosa and Their cAMP‐Decreasing Activities
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ChemInform Abstract: Kalmanol, a Pharmacologically Active Diterpenoid with a New Ring Skeleton from Kalmia angustifolia L.
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Discovery of Kalmane Diterpenoids as Potent Analgesics from the Flowers of Rhododendron dauricum
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Diversity‐Oriented Approach to Carbocycles and Heterocycles through Ring‐Rearrangement Metathesis, Fischer Indole Cyclization, and Diels–Alder Reaction as Key Steps
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Pyrolaceae
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Grayanoids from the Ericaceae family: structures, biological activities and mechanism of action
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Grayanoid diterpene insect antifeedants and insecticides from Rhododendron molle
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The [4 + 4] cycloaddition and its strategic application in natural product synthesis
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Construction of polyfunctionalized seven-membered rings by the cyclization of 2,3-epoxy alcohols
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Antinociceptive grayanane-derived diterpenoids from flowers of Rhododendron molle
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Diterpenoids with diverse carbon skeletons from the roots of Pieris formosa and their analgesic and antifeedant activities
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.bse.2020.104129openalex-snapshot
Chemical constituents from the leaves of Lyonia ovalifolia var. hebecarpa
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An overview of grayanane diterpenoids and their biological activities from the Ericaceae family in the last seven years
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Diverse epoxy grayanane diterpenoids with analgesic activity from the roots of Pieris formosa
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The efficacy and toxicity of grayanoids as analgesics: A systematic review
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Grayanane and leucothane diterpenoids from the leaves of Rhododendron micranthum
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Studies on the synthetic utility of [6+3] cycloaddition of pentafulvenes with 3-oxidopyrylium betaines: efficient synthesis of fused ring cyclooctanoids
inferred← citeshttps://doi.org/10.1016/j.tet.2023.133384openalex-snapshot
Asymmetric synthesis of a versatile 1,2,3-trisubstituted cyclopentane synthetic building block
inferred← citeshttps://doi.org/10.1016/s0040-4020(00)00789-4openalex-snapshot
Oxygen-Directed Carbocyclizations of Epoxides
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)80982-0openalex-snapshot
Stereocontrolled syntheses of hydroxylated tricyclic systems by a new annulation of 2-cyclohexen-1-one
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The synthesis of carbocyclic eight-membered rings
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On palladium catalyzed cyclizations to medium sized carbocycles
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An efficient approach to bridged-bicyclic rings via intramolecular diazo ketone insertion
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Bioinspired Total Synthesis of Natural Products
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Highly Oxygenated Grayanane Diterpenoids from Flowers of Pieris japonica and Structure–Activity Relationships of Antifeedant Activity against Pieris brassicae
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.5c01252openalex-snapshot
Bioinspired Chemical Transformations of Grayanotoxin III to Kalmanol, seco -Rhodomollone, and Rhodomolleins XXIII and XXIV
inferred← citeshttps://doi.org/10.1021/acs.joc.3c00365openalex-snapshot
Enantioselective Total Syntheses of Grayanane Diterpenoids and (+)-Kalmanol: Evolution of the Bridgehead Carbocation-Based Cyclization and Late-Stage Functional Group Manipulation Strategies
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c00885openalex-snapshot
Forging the Tetracyclic Core Framework of Rhodomolleins XIV and XLII: A Ring-Distortion Approach
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Synthesis of Polyquinane Natural Products: An Update
inferred← citeshttps://doi.org/10.1021/cr9800356openalex-snapshot
Progress in the Construction of Cyclooctanoid Systems: New Approaches and Applications to Natural Product Syntheses
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inferred← citeshttps://doi.org/10.1021/ja044542iopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ja204289qopenalex-snapshot
From Highly Enantioselective Catalytic Reaction of 1,3-Diynes with Aldehydes to Facile Asymmetric Synthesis of Polycyclic Compounds
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1021/jo951994sopenalex-snapshot
Cyclization to Stereoisomeric Hexahydro-3,6-pentaleno[1,6-cd]pyran- 1(3H)-ones. A Model Study Explains the Preference for Trans Products
inferred← citeshttps://doi.org/10.1021/jo980986jopenalex-snapshot
Oxygen-Directed Carbocyclizations of 2,3-Epoxy Alcohols: Stereoselective Construction of Polyfunctionalized Seven-Membered Rings by 7-Endo-Tet Ring Closures
inferred← citeshttps://doi.org/10.1021/np500074qopenalex-snapshot
Diterpenoids from the Flowers of Rhododendron molle
inferred← citeshttps://doi.org/10.1021/ol1002797openalex-snapshot
Highly Acylated Diterpenoids with a New 3,4-Secograyanane Skeleton from the Flower Buds ofRhododendron molle
inferred← citeshttps://doi.org/10.1021/ol401292yopenalex-snapshot
Micranthanone A, a New Diterpene with an Unprecedented Carbon Skeleton from Rhododendron micranthum
inferred← citeshttps://doi.org/10.1021/ol5020653openalex-snapshot
Mollanol A, a Diterpenoid with a New C-Nor-D-homograyanane Skeleton from the Fruits of Rhododendron molle
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/c7ra08635kopenalex-snapshot
Biological and chemical guided isolation of 3,4-secograyanane diterpenoids from the roots of Pieris formosa
inferred← citeshttps://doi.org/10.1039/c9ra01736dopenalex-snapshot
Micranthanosides I and II, two novel 1,10-secograyanane diterpenoids and their antinociceptive analogues from the leaves and twigs of Rhododendron micranthum
inferred← citeshttps://doi.org/10.1076/phbi.36.4.237.4583openalex-snapshot
Survey of Secondary Plant Metabolites with Cardiovascular Activity
inferred← citeshttps://doi.org/10.1080/10286020903436519openalex-snapshot
New grayanol diterpenoid and new phenolic glucoside from the flowers ofPieris formosa
inferred← citeshttps://doi.org/10.1139/y07-108openalex-snapshot
Medicinal plants of Cree communities (Québec, Canada): antioxidant activity of plants used to treat type 2 diabetes symptomsThis article is one of a selection of papers published in this special issue (part 2 of 2) on the Safety and Efficacy of Natural Health Products.
inferred← citeshttps://doi.org/10.3184/003685016x14720691270831openalex-snapshot
From ‘Mad Honey’ to Hypotensive Agents, the Grayanoid Diterpenes
inferred← citeshttps://doi.org/10.3390/antiox10091373openalex-snapshot
Antioxidant, Anti-Inflammatory, and Anti-Aging Potential of a Kalmia angustifolia Extract and Identification of Some Major Compounds
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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