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Hunterines A–C, Three Unusual Monoterpenoid Indole Alkaloids from Hunteria zeylanica
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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/anie.201505198openalex-snapshot
Biomimetic Total Syntheses of (−)‐Leucoridines A and C through the Dimerization of (−)‐Dihydrovalparicine
inferredcites →https://doi.org/10.1002/anie.201710943openalex-snapshot
Total Syntheses of the Monoterpenoid Indole Alkaloids (±)‐Alstoscholarisine B and C
inferredcites →https://doi.org/10.1007/s10600-010-9494-8openalex-snapshot
Indole alkaloids from leaves and stems of Hunteria zeylanica
inferredcites →https://doi.org/10.1016/j.phytochem.2014.07.023openalex-snapshot
Phytochemical genomics of the Madagascar periwinkle: Unravelling the last twists of the alkaloid engine
inferredcites →https://doi.org/10.1016/j.tetlet.2016.03.019openalex-snapshot
Polyneuridine aldehyde: structure, stability overviews and a plausible origin of flavopereirine
inferredcites →https://doi.org/10.1016/j.tetlet.2017.05.094openalex-snapshot
Meloslines A and B, two novel indole alkaloids from Alstonia scholaris
inferredcites →https://doi.org/10.1016/s0014-2999(97)01097-2openalex-snapshot
Inhibitory effects of corymine, an alkaloidal component from the leaves of Hunteria zeylanica, on glycine receptors expressed in Xenopus oocytes
inferredcites →https://doi.org/10.1016/s0031-9422(00)89602-8openalex-snapshot
Indole alkaloids fromTabernaemontana glandulosa
inferredcites →https://doi.org/10.1016/s0040-4039(00)95417-0openalex-snapshot
A biomimetic entry in the hexacyclic tuboxenin ring system methylene-indolines, indolenines and indoleniniums, XXII
inferredcites →https://doi.org/10.1021/acs.jnatprod.5b00051openalex-snapshot
Ervatamines A–I, Anti-inflammatory Monoterpenoid Indole Alkaloids with Diverse Skeletons fromErvatamia hainanensis
inferredcites →https://doi.org/10.1021/acs.jnatprod.5b01035openalex-snapshot
Indole Alkaloids from Hunteria zeylanica
inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00011openalex-snapshot
Melokhanines A–J, Bioactive Monoterpenoid Indole Alkaloids with Diverse Skeletons from Melodinus khasianus
inferredcites →https://doi.org/10.1021/acs.joc.8b01371openalex-snapshot
Ervadivamines A and B, Two Unusual Trimeric Monoterpenoid Indole Alkaloids from Ervatamia divaricata
inferredcites →https://doi.org/10.1021/acs.orglett.5b03583openalex-snapshot
Alstoscholarisines H–J, Indole Alkaloids from Alstonia scholaris: Structural Evaluation and Bioinspired Synthesis of Alstoscholarisine H
inferredcites →https://doi.org/10.1021/acs.orglett.7b00983openalex-snapshot
Total Syntheses of Naucleamides A–C and E, Geissoschizine, Geissoschizol, (E)-Isositsirikine, and 16-epi-(E)-Isositsirikine
inferredcites →https://doi.org/10.1021/acs.orglett.7b02445openalex-snapshot
Tabercorymines A and B, Two Vobasinyl–Ibogan-Type Bisindole Alkaloids from Tabernaemontana corymbosa
inferredcites →https://doi.org/10.1021/acs.orglett.7b02463openalex-snapshot
Gelsekoumidines A and B: Two Pairs of Atropisomeric Bisindole Alkaloids from the Roots of Gelsemium elegans
inferredcites →https://doi.org/10.1021/acs.orglett.8b03592openalex-snapshot
Alstoscholactine and Alstolaxepine, Monoterpenoid Indole Alkaloids with γ-Lactone-Bridged Cycloheptane and Oxepane Moieties from Alstonia scholaris
inferredcites →https://doi.org/10.1021/acs.orglett.9b00230openalex-snapshot
Alstonlarsines A–D, Four Rearranged Indole Alkaloids from Alstonia scholaris
inferredcites →https://doi.org/10.1021/cr000665jopenalex-snapshot
The Assignment of Absolute Configuration by NMR
inferredcites →https://doi.org/10.1021/ja00538a043openalex-snapshot
Structure of goniomine, an alkaloid of a new type biogenetically related to indole alkaloids. X-ray analysis of dihydrogoniomine
inferredcites →https://doi.org/10.1021/jo1006762openalex-snapshot
Bisnicalaterines B and C, Atropisomeric Bisindole Alkaloids fromHunteria zeylanica, Showing Vasorelaxant Activity
inferredcites →https://doi.org/10.1021/np1001187openalex-snapshot
Leucoridines A−D, Cytotoxic Strychnos−Strychnos Bisindole Alkaloids from Leuconotis
inferredcites →https://doi.org/10.1021/np500240bopenalex-snapshot
Iboga-Type Alkaloids from Ervatamia officinalis
inferredcites →https://doi.org/10.1021/ol1000022openalex-snapshot
Melotenine A, a Cytotoxic Monoterpenoid Indole Alkaloid from Melodinus tenuicaudatus
inferredcites →https://doi.org/10.1021/ol301745bopenalex-snapshot
Ilelic Acids A and B, Two Unusual Triterpenes with a Seven-Membered Ring from Ilex latifolia
inferredcites →https://doi.org/10.1021/ol500231copenalex-snapshot
Palladium-Catalyzed Direct Arylation of Indoles with Cyclohexanones
inferredcites →https://doi.org/10.1021/ol5029223openalex-snapshot
Indole Alkaloids with New Skeleton Activating Neural Stem Cells
inferredcites →https://doi.org/10.1021/ol9018826openalex-snapshot
Melohenines A and B, Two Unprecedented Alkaloids from Melodinus henryi
inferredcites →https://doi.org/10.1039/b512615kopenalex-snapshot
Chemistry and biology of monoterpene indole alkaloid biosynthesis
inferredcites →https://doi.org/10.1039/c4gc00840eopenalex-snapshot
Brønsted acid ionic liquid catalyzed facile synthesis of 3-vinylindoles through direct C3 alkenylation of indoles with simple ketones
inferredcites →https://doi.org/10.1039/c6ra16762dopenalex-snapshot
Melohemsines A-I, melodinus-type alkaloids from Melodinus hemsleyanus
inferredcites →https://doi.org/10.1107/s0108767399004262openalex-snapshot
Absolute structure and absolute configuration
inferredcites →https://doi.org/10.1126/science.aat4100openalex-snapshot
Missing enzymes in the biosynthesis of the anticancer drug vinblastine in Madagascar periwinkle
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.2022.113280zenodo-depositor-declared
Triterpenoids from the fruits of Melia azedarach L. and their cytotoxic activities
inferred← citeshttps://doi.org/10.1002/chem.202404501openalex-snapshot
Bioinspired Synthesis of (−)‐Hunterine A: Deciphering the Key Step in the Biogenetic Pathway
inferred← citeshttps://doi.org/10.1007/s11101-024-10015-3openalex-snapshot
Exploring plant-derived bisindole alkaloids: a comprehensive review of sources, phytochemistry and cytotoxicity
inferred← citeshttps://doi.org/10.1016/j.fitote.2020.104685openalex-snapshot
New cytotoxic secondary metabolites against human pancreatic cancer cells from the Hypericum perforatum endophytic fungus Aspergillus terreus
inferred← citeshttps://doi.org/10.1016/j.fitote.2023.105430openalex-snapshot
The current scenario of naturally occurring indole alkaloids with anticancer potential
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113678openalex-snapshot
Monoterpenoid indole alkaloid adducts and dimers from Melodinus fusiformis
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114245openalex-snapshot
Kopsileuconines A−D: Bisindole alkaloids with cytotoxic activity from Kopsia hainanensis
inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114550openalex-snapshot
Mavacurane–aspidospermane bisindole alkaloids from Hunteria zeylanica: structural elucidation and revision, bioinspired semisynthesis and cytotoxicity
inferred← citeshttps://doi.org/10.1016/s1875-5364(19)30113-xopenalex-snapshot
Four new corynanthe-type alkaloids from the roots of Alstonia scholaris
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00925openalex-snapshot
Structurally Diverse Indole Alkaloids with Vasorelaxant Activity from Melodinus hemsleyanus
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b01151openalex-snapshot
Bioactive Limonoids and Triterpenoids from the Fruits of Melia azedarach
inferred← citeshttps://doi.org/10.1021/acs.joc.0c01448openalex-snapshot
Hunzeylanines A–E, Five Bisindole Alkaloids Tethered with a Methylene Group from the Roots of Hunteria zeylanica
inferred← citeshttps://doi.org/10.1021/acs.joc.3c00369openalex-snapshot
Alashanines A–C, Three Quinone-Terpenoid Alkaloids from Syringa pinnatifolia with Cytotoxic Potential by Activation of ERK
inferred← citeshttps://doi.org/10.1021/acs.joc.3c00765openalex-snapshot
Resolving a Natural Product Cold Case: Elucidation of Fusapyrone Structure and Absolute Configuration and Demonstration of Their Fungal Biofilm Disrupting Properties
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c04075openalex-snapshot
Photocatalyzed Dearomative [2 + 2] Cycloaddition of Indoles with Alkynes to Access Cyclobutene-Fused Indolines
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c04997openalex-snapshot
Hunterlanines A–F, Neuroprotective Monoterpenoid Indole Alkaloid Heterodimers from Hunteria zeylanica
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b04398openalex-snapshot
Chalcone-Based Pyridinium Salts and Their Diastereoselective Dearomatization To Access Bibridged Benzoazepines
inferred← citeshttps://doi.org/10.1021/jacs.3c13590openalex-snapshot
Enantioselective Total Synthesis of (−)-Hunterine A Enabled by a Desymmetrization/Rearrangement Strategy
inferred← citeshttps://doi.org/10.1021/jacs.4c06569openalex-snapshot
Merging Ring-Opening 1,2-Metallate Shift with Asymmetric C(sp3)–H Borylation of Aziridines
inferred← citeshttps://doi.org/10.1039/d0qo00751jopenalex-snapshot
Alstolarines A and B, two unusual monoterpenoid indole alkaloids with an acetal moiety from Alstonia scholaris
inferred← citeshttps://doi.org/10.1039/d4gc04126gopenalex-snapshot
Electrochemically enabled dearomative [2 + 2] cycloadditions of indoles with alkynes to access cyclobutene-fused indolines
inferred← citeshttps://doi.org/10.1039/d5ra04921kopenalex-snapshot
A review on the sulfur ylide-mediated Corey–Chaykovsky reaction: a powerful approach to natural product synthesis
inferred← citeshttps://doi.org/10.1039/d6ra05651bopenalex-snapshot
Molecular rearrangements as powerful tools in diversity-oriented natural products synthesis: a review
inferred← citeshttps://doi.org/10.1080/10286020.2020.1844675openalex-snapshot
Survey of natural products reported by Asian research groups in 2019
inferred← citeshttps://doi.org/10.1080/14786419.2026.2652068openalex-snapshot
Unlocking the cytotoxic potential of Apocynaceae monoterpene indole and bis -indole alkaloids: a review
inferred← citeshttps://doi.org/10.2174/9798898810276125010007openalex-snapshot
Efficient Synthesis of Quinone-Based Glycohybrids
inferred← citeshttps://doi.org/10.3762/bjoc.21.164openalex-snapshot
The application of desymmetric enantioselective reduction of cyclic 1,3-dicarbonyl compounds in the total synthesis of terpenoid and alkaloid natural products
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