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Hyperuralones A and B, New Acylphloroglucinol Derivatives with Intricately Caged Cores from Hypericum uralum
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1439-7633(20011203)2:12<873::aid-cbic873>3.0.co;2-aopenalex-snapshot
Diels-Alderases
inferredcites →https://doi.org/10.1002/anie.199602891openalex-snapshot
Pericyclic Reactions in Biological Systems—Does Nature Know About the Diels—Alder Reaction?
inferredcites →https://doi.org/10.1002/anie.200200534openalex-snapshot
Chemistry and Biology of Biosynthetic Diels–Alder Reactions
inferredcites →https://doi.org/10.1002/anie.201103873openalex-snapshot
The Chemistry of the Polycyclic Polyprenylated Acylphloroglucinols
inferredcites →https://doi.org/10.1016/0031-9422(88)80148-1openalex-snapshot
Nemorosonol, a derivative of tricyclo-[4.3.1.03,7]-Decane-7-hydroxy-2,9-dione from Clusia nemorosa
inferredcites →https://doi.org/10.1016/0031-9422(93)85248-popenalex-snapshot
Nemorosonol, a derivative of tricyclo-[4.3.1.03,7]-Decane-7-hydroxy-2,9-dione from Clusia nemorosa
inferredcites →https://doi.org/10.1016/j.tet.2005.05.091openalex-snapshot
Further rearranged prenylxanthones and benzophenones from Garcinia bracteata
inferredcites →https://doi.org/10.1021/cr0500582openalex-snapshot
Polycyclic Polyprenylated Acylphloroglucinols
inferredcites →https://doi.org/10.1021/ja003216+openalex-snapshot
Lovastatin Nonaketide Synthase Catalyzes an Intramolecular Diels−Alder Reaction of a Substrate Analogue
inferredcites →https://doi.org/10.1021/ja1057828openalex-snapshot
Catalytic Enantioselective Alkylative Dearomatization−Annulation: Total Synthesis and Absolute Configuration Assignment of Hyperibone K
inferredcites →https://doi.org/10.1021/ja312150dopenalex-snapshot
Enantioselective Total Synthesis of Hyperforin
inferredcites →https://doi.org/10.1021/ja5060302openalex-snapshot
Rapid Synthesis of Polyprenylated Acylphloroglucinol Analogs via Dearomative Conjunctive Allylic Annulation
inferredcites →https://doi.org/10.1021/jm0209782openalex-snapshot
Biosynthesis of Hyperforin in Hypericum perforatum
inferredcites →https://doi.org/10.1021/jp0275802openalex-snapshot
Systematic Investigation of Modern Quantum Chemical Methods to Predict Electronic Circular Dichroism Spectra
inferredcites →https://doi.org/10.1021/ol050960wopenalex-snapshot
Biyouyanagin A, an Anti-HIV Agent from Hypericum chinense L. var. salicifolium
inferredcites →https://doi.org/10.1021/ol101380aopenalex-snapshot
Biomimetic Synthesis of Polycyclic Polyprenylated Acylphloroglucinol Natural Products Isolated from Hypericum papuanum
inferredcites →https://doi.org/10.1021/ol302524qopenalex-snapshot
Biomimetic Total Synthesis of (±)-Garcibracteatone
inferredcites →https://doi.org/10.1021/ol500808popenalex-snapshot
New Acylphloroglucinol Derivatives with Diverse Architectures from Hypericum henryi
inferredcites →https://doi.org/10.1021/ol9028435openalex-snapshot
How an Enzyme Might Accelerate an Intramolecular Diels−Alder Reaction: Theozymes for the Formation of Salvileucalin B
inferredcites →https://doi.org/10.1039/b305068hopenalex-snapshot
Enzymatic catalysis of the Diels–Alder reaction in the biosynthesis of natural products
inferredcites →https://doi.org/10.1039/b600518gopenalex-snapshot
Phloroglucinol compounds of natural origin
inferredcites →https://doi.org/10.1039/b914364popenalex-snapshot
Phloroglucinol compounds of natural origin: Synthetic aspects
inferredcites →https://doi.org/10.1039/c2cc32352dopenalex-snapshot
Hypercohin A, a new polycyclic polyprenylated acylphloroglucinol possessing an unusual bicyclo[5.3.1]hendecane core from Hypericum cohaerens
inferredcites →https://doi.org/10.1039/c2ob25827gopenalex-snapshot
Concerted, highly asynchronous, enzyme-catalyzed [4 + 2] cycloaddition in the biosynthesis of spinosyn A; computational evidence
inferredcites →https://doi.org/10.1074/jbc.m003119200openalex-snapshot
Detailed Reaction Mechanism of Macrophomate Synthase
inferredcites →https://doi.org/10.1246/bcsj.78.537openalex-snapshot
Involvement of the Diels–Alderases in the Biosynthesis of Natural Products
inferredcites →https://doi.org/10.2174/1385272802666220128214243openalex-snapshot
Diels-Aider Type Natural Products - Structures and Biosynthesis
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.2021.112771zenodo-depositor-declared
Structurally diverse polyprenylated acylphloroglucinols from Hypericum uralum Buch.-Ham. ex D. Don
inferred← citeshttps://doi.org/10.1002/cjoc.202400248openalex-snapshot
Hyperlanins A and B, Two Highly Rearranged Meroterpenoids from Hypericum lancasteri
inferred← citeshttps://doi.org/10.1002/cjoc.202400739openalex-snapshot
Hyperkouytones A—O, New Polyprenylated Acylphloroglucinols from Hypericum kouytchense with Multidrug Resistance Reversal Activity
inferred← citeshttps://doi.org/10.1007/978-981-99-7329-3_7openalex-snapshot
Classification of Diverse Novel Phloroglucinols
inferred← citeshttps://doi.org/10.1007/s11426-016-0052-4openalex-snapshot
Polyprenylated acylphloroglucinols from the fruits of Hypericum henryi
inferred← citeshttps://doi.org/10.1007/s13659-019-00229-wopenalex-snapshot
Dearomatized Isoprenylated Acylphloroglucinol Derivatives with Potential Antitumor Activities from Hypericum henryi
inferred← citeshttps://doi.org/10.1007/s13659-019-0206-1openalex-snapshot
Diverse Polyphenols from Hypericum faberi
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.03.025openalex-snapshot
Hyperpatulols A–I, spirocyclic acylphloroglucinol derivatives with anti-migration activities from the flowers of Hypericum patulum
inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.106005openalex-snapshot
Diverse polycyclic polyprenylated acylphloroglucinols with anti-neuroinflammatory activity from Hypericum beanii
inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.109134openalex-snapshot
Polycyclic Polyprenylated Acylphloroglucinols from Hypericum Hookerianum with their immunosuppressive activities
inferred← citeshttps://doi.org/10.1016/j.bmcl.2017.09.001openalex-snapshot
Polycyclic polyprenylated acylphloroglucinol derivatives from Hypericum scabrum
inferred← citeshttps://doi.org/10.1016/j.cclet.2016.11.014openalex-snapshot
Hyperisampsins N and O, two new benzoylated phloroglucinol derivatives from Hypericum sampsonii
inferred← citeshttps://doi.org/10.1016/j.cplett.2020.138206openalex-snapshot
Physical mechanism and electric-magnetic interaction in ECD and ROA: Visualization methods on chirality
inferred← citeshttps://doi.org/10.1016/j.fitote.2016.10.014openalex-snapshot
Chiral separation and absolute configurations of two pairs of racemic polyprenylated benzophenones from Hypericum sampsonii
inferred← citeshttps://doi.org/10.1016/j.fitote.2017.12.020openalex-snapshot
Hyperattenins L and M, two new polyprenylated acylphloroglucinols with adamantyl and homoadamantyl core structures from Hypericum attenuatum
inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105249openalex-snapshot
Bioactive polycyclic polyprenylated acylphloroglucinols from Hypericum scabrum
inferred← citeshttps://doi.org/10.1016/j.fitote.2026.107251openalex-snapshot
Bioactive polycyclic polyprenylated acylphloroglucinols from Hypericum maclarenii
inferred← citeshttps://doi.org/10.1016/j.hermed.2026.101100openalex-snapshot
Gynaecological healing: exploring traditional ethno-medicinal plants of Himachal Pradesh, India
inferred← citeshttps://doi.org/10.1016/j.phytochem.2018.08.002openalex-snapshot
Structural diversity and biological activities of phloroglucinol derivatives from Hypericum species
inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114561openalex-snapshot
Hyperwilsol A, a highly modified 2-nor-polycyclic polyprenylated acylphloroglucinol possessing an unusual 6/6/5/5 spirotetracyclic skeleton from Hypericum wilsonii
inferred← citeshttps://doi.org/10.1016/j.phytol.2020.09.016openalex-snapshot
Antimicrobial polycyclic polyprenylated acylphoroglucinols from Mesua ferrea flower
inferred← citeshttps://doi.org/10.1016/j.tet.2016.04.025openalex-snapshot
Unusual adamantane type polyprenylated acylphloroglucinols with an oxirane unit and their structural transformation from Hypericum hookerianum
inferred← citeshttps://doi.org/10.1016/j.tet.2016.06.035openalex-snapshot
Hyperhexanone A, a crucial intermediate from bicyclo[3.3.1]- to cyclohexanone monocyclic-polycyclic polyprenylated acylphloroglucinols
inferred← citeshttps://doi.org/10.1016/j.tet.2016.12.042openalex-snapshot
homo-adamantane type polyprenylated acylphloroglucinols from Hypericum pseudohenryi
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.02.056openalex-snapshot
Two new adamantyl-like polyprenylated acylphloroglucinols from Hypericum attenuatum choisy
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.08.033openalex-snapshot
Hypercohin K, a polycyclic polyprenylated acylphloroglucinol with an unusual spiro-fused cyclopropane ring from Hypericum cohaerens
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.11.058openalex-snapshot
Hyperjapones F–I, terpenoid polymethylated acylphloroglucinols from Hypericum japonicum
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.04.044openalex-snapshot
seco-Polycyclic polyprenylated acylphloroglucinols with unusual carbon skeletons from Hypericum ascyron
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.09.071openalex-snapshot
Spirocyclic polycyclic polyprenylated acylphloroglucinols from the ethyl acetate fraction of Hypericum henryi
inferred← citeshttps://doi.org/10.1016/s1875-5364(24)60599-6openalex-snapshot
Hyparillums A and B: polycyclic polyprenylated acylphloroglucinols from Hypericum patulum
inferred← citeshttps://doi.org/10.1021/acs.chemrev.7b00551openalex-snapshot
Research Progress of Polycyclic Polyprenylated Acylphloroglucinols
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c01202openalex-snapshot
Diverse Polycyclic Polyprenylated Acylphloroglucinol Congeners with Anti-Nonalcoholic Steatohepatitis Activity from Hypericum forrestii
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00057openalex-snapshot
Polycyclic Polyprenylated Acylphloroglucinol Congeners Possessing Diverse Structures from Hypericum henryi
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00066openalex-snapshot
Hypermongones A–J, Rare Methylated Polycyclic Polyprenylated Acylphloroglucinols from the Flowers of Hypericum monogynum
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00667openalex-snapshot
Polycyclic Polyprenylated Derivatives from Hypericum uralum: Neuroprotective Effects and Antidepressant-like Activity of Uralodin A
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00830openalex-snapshot
1,9-seco-Bicyclic Polyprenylated Acylphloroglucinols from Hypericum uralum
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00754openalex-snapshot
Skeleton Reassignment of Type C Polycyclic Polyprenylated Acylphloroglucinols
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b01006openalex-snapshot
Prenylated Acylphloroglucinols from Hypericum faberi
inferred← citeshttps://doi.org/10.1021/acs.joc.6b01016openalex-snapshot
Visible-Light-Promoted Oxidative [4 + 2] Cycloadditions of Aryl Silyl Enol Ethers
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c01745openalex-snapshot
Total Synthesis of a PPAP, Nemorosonol, Using a Tandem Michael Addition–Intramolecular Aldol Reaction
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00100openalex-snapshot
Hypersubones A and B, New Polycyclic Acylphloroglucinols with Intriguing Adamantane Type Cores from Hypericum subsessile
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00588openalex-snapshot
Two Unusual Polycyclic Polyprenylated Acylphloroglucinols, Including a Pair of Enantiomers from Garcinia multiflora
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00650openalex-snapshot
Hyperjapones A–E, Terpenoid Polymethylated Acylphloroglucinols from Hypericum japonicum
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02725openalex-snapshot
Hypatulins A and B, Meroterpenes from Hypericum patulum
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b04022openalex-snapshot
Norascyronones A and B, 2,3,4-nor-Polycyclic Polyprenylated Acylphloroglucinols from Hypericum ascyron
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00388openalex-snapshot
Garsubelone A, the First Dimeric Polycyclic Polyprenylated Acylphloroglucinols with Complicated Heptacyclic Architecture from Garcinia subelliptica
inferred← citeshttps://doi.org/10.1021/acsomega.3c04947openalex-snapshot
Garbractin A, a Polycyclic Polyprenylated Acylphloroglucinol with a 4,11-dioxatricyclo[4.4.2.01,5]Dodecane Skeleton from Garcinia bracteata Fruits
inferred← citeshttps://doi.org/10.1021/jf505982fopenalex-snapshot
Characterization of Phenolic Constituents Inhibiting the Formation of Sulfur-Containing Volatiles Produced during Garlic Processing
inferred← citeshttps://doi.org/10.1021/np5009784openalex-snapshot
Friedel–Crafts Alkylation of Acylphloroglucinols Catalyzed by a Fungal Indole Prenyltransferase
inferred← citeshttps://doi.org/10.1021/ol5030579openalex-snapshot
Bioactive Acylphloroglucinols with Adamantyl Skeleton from Hypericum sampsonii
inferred← citeshttps://doi.org/10.1038/srep14772openalex-snapshot
Hyperisampsins H–M, Cytotoxic Polycyclic Polyprenylated Acylphloroglucinols from Hypericum sampsonii
inferred← citeshttps://doi.org/10.1039/c5ra26332hopenalex-snapshot
Hypersampsones S–W, new polycyclic polyprenylated acylphloroglucinols from Hypericum sampsonii
inferred← citeshttps://doi.org/10.1039/c6qo00620eopenalex-snapshot
Furanmonogones A and B: two rearranged acylphloroglucinols with a 4,5-seco-3(2H)-furanone core from the flowers of Hypericum monogynum
inferred← citeshttps://doi.org/10.1039/c6ra08805hopenalex-snapshot
Polycyclic polyprenylated acylphloroglucinols: natural phosphodiesterase-4 inhibitors from Hypericum sampsonii
inferred← citeshttps://doi.org/10.1039/c6ra17885eopenalex-snapshot
Sampbenzophenones A–G, prenylated benzoylphloroglucinol derivatives from Hypericum sampsonii
inferred← citeshttps://doi.org/10.1039/c7ra01543gopenalex-snapshot
Adamantyl derivatives and rearranged benzophenones from Garcinia xanthochymus fruits
inferred← citeshttps://doi.org/10.1039/c7ra05947gopenalex-snapshot
Norsampsone E, an unprecedented decarbonyl polycyclic polyprenylated acylphloroglucinol with a homoadamantyl core from Hypericum sampsonii
inferred← citeshttps://doi.org/10.1039/c8ra05322gopenalex-snapshot
Hyperelatosides A–E, biphenyl ether glycosides from Hypericum elatoides , with neurotrophic activity
inferred← citeshttps://doi.org/10.1080/02652048.2019.1631400openalex-snapshot
Potential antioxidant and anti-inflammatory action of Hypericum hookerianum extracts in a liposome system evaluated with zebrafish embryos
inferred← citeshttps://doi.org/10.3390/molecules24193568openalex-snapshot
Cytotoxic Xanthones from Hypericum stellatum, an Ethnomedicine in Southwest China
inferred← citeshttps://doi.org/10.3390/plants12071500openalex-snapshot
Cytotoxic and Antibacterial Prenylated Acylphloroglucinols from Hypericum olympicum L.
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.82.1184openalex-snapshot
Total Synthesis of Fused Natural Products
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