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Bioactive Terpenoids from the Fruits of Aphanamixis grandifolia
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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.197903631openalex-snapshot
Circular Dichroism and Absolute Conformation: Application of Qualitative MO Theory to Chiroptical Phenomena
inferredcites →https://doi.org/10.1002/cjoc.201200309openalex-snapshot
Four New Limonoids from Aphanamixis grandifolia
inferredcites →https://doi.org/10.1002/hlca.200790080openalex-snapshot
Chemical Constituents of Polyalthia nemoralis
inferredcites →https://doi.org/10.1007/bf01949897openalex-snapshot
The structure of amoorastatone and the cytotoxic limonoid 12-hydroxyamoorastatin
inferredcites →https://doi.org/10.1016/j.bmc.2011.01.007openalex-snapshot
Chisopanins A–K, 11 new protolimonoids from Chisocheton paniculatus and their anti-inflammatory activities
inferredcites →https://doi.org/10.1016/j.phytochem.2003.08.020openalex-snapshot
Ring A-seco mosquito larvicidal limonoids from Turraea wakefieldii
inferredcites →https://doi.org/10.1016/j.phytochem.2010.08.017openalex-snapshot
Cytotoxic tirucallane C26 triterpenoids from the stem barks of Aphanamixis grandifolia
inferredcites →https://doi.org/10.1016/j.phytochem.2012.05.017openalex-snapshot
2,3-Seco- and 3,4-seco-tirucallane triterpenoid derivatives from the stems of Aphanamixis grandifolia Blume
inferredcites →https://doi.org/10.1016/j.phytol.2011.05.003openalex-snapshot
Limonoids from the fruits of Melia toosendan
inferredcites →https://doi.org/10.1016/j.tet.2012.03.083openalex-snapshot
Aphanalides A–H, ring A-seco limonoids from the fruits of Aphanamixis polystachya
inferredcites →https://doi.org/10.1016/j.tetlet.2012.01.061openalex-snapshot
A pair of tirucallane C27-triterpenoid cyclopentenone epimers from the stem barks of Aphanamixis grandifolia
inferredcites →https://doi.org/10.1016/s0031-9422(00)00482-9openalex-snapshot
ent-Pimarane derivatives from Dysoxylum hainanense
inferredcites →https://doi.org/10.1016/s0040-4020(02)00679-8openalex-snapshot
Three new apo-tirucallols with six-membered hemiacetal from Meliaceae
inferredcites →https://doi.org/10.1016/s0040-4039(01)86149-9openalex-snapshot
Evodulone, a new tetranortriterpenoid from carapa procera
inferredcites →https://doi.org/10.1021/ja00476a065openalex-snapshot
Antineoplastic agents. 57. Isolation and structure of aphanastatin
inferredcites →https://doi.org/10.1021/ja00492a051openalex-snapshot
Antineoplastic agents. 61. Isolation and structure of amoorastatin
inferredcites →https://doi.org/10.1021/jf205362dopenalex-snapshot
The Limonoids and Their Antitobacco Mosaic Virus (TMV) Activities from Munronia unifoliolata Oliv.
inferredcites →https://doi.org/10.1021/jo010136vopenalex-snapshot
Determination of Absolute Configuration of Acyclic 1,2-Diols with Mo2(OAc)4. 1. Snatzke's Method Revisited
inferredcites →https://doi.org/10.1021/jo062445xopenalex-snapshot
Practical Method for the Absolute Configuration Assignment of tert / tert 1,2-Diols Using Their Complexes with Mo 2 (OAc) 4
inferredcites →https://doi.org/10.1021/np0702842openalex-snapshot
Agladupols A–E, Triterpenoids from Aglaia duperreana
inferredcites →https://doi.org/10.1021/np2006296openalex-snapshot
Tirucallane-Type Triterpenoids from Dysoxylum lenticellatum
inferredcites →https://doi.org/10.1021/np990322kopenalex-snapshot
New Terpenoids from Maytenus blepharodes
inferredcites →https://doi.org/10.1021/ol902565sopenalex-snapshot
Structure Determination of Grandifotane A from Khaya grandifoliola by NMR, X-ray Diffraction, and ECD Calculation
inferredcites →https://doi.org/10.1107/s0108767383001762openalex-snapshot
On enantiomorph-polarity estimation
inferredcites →https://doi.org/10.1177/1934578x1100600304openalex-snapshot
Melidianolic Acid A and B, New Antimalarial Acyclic Diterpenes from Aphanamixis grandifolia
inferredcites →https://doi.org/10.1248/cpb.55.1442openalex-snapshot
Apotirucallane and Tirucallane Triterpenoids from Cedrela sinensis
inferredcites →https://doi.org/10.1248/cpb.c12-00332openalex-snapshot
Polystanins A–D, Four New Protolimonoids from the Fruits of Aphanamixis polystachya
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Triterpenoids from the fruits of Melia azedarach L. and their cytotoxic activities
inferred← citeshttps://doi.org/10.1002/ejoc.201700795openalex-snapshot
Aphapolins A and B: Two Nemoralisin Diterpenoids Isolated from Aphanamixis polystachya (Wall.) R. Parker
inferred← citeshttps://doi.org/10.1007/s00706-018-2152-8openalex-snapshot
Facile synthesis of 3(2H)-furanones
inferred← citeshttps://doi.org/10.1007/s00709-019-01411-0openalex-snapshot
Plant triterpenoid saponins: biosynthesis, in vitro production, and pharmacological relevance
inferred← citeshttps://doi.org/10.1007/s10600-025-04566-wopenalex-snapshot
A New Terpenoid from the Leaves of Aphanamixis polystachya
inferred← citeshttps://doi.org/10.1007/s11101-013-9317-1openalex-snapshot
Constituents from Aphanamixis species and their biological activities
inferred← citeshttps://doi.org/10.1007/s11101-025-10110-zopenalex-snapshot
Diterpenoid compounds derived from meliaceae plants and biological activities
inferred← citeshttps://doi.org/10.1007/s13659-014-0006-6openalex-snapshot
Diterpenoids and Limonoids from the Leaves and Twigs of Swietenia mahagoni
inferred← citeshttps://doi.org/10.1007/s13659-020-00274-wopenalex-snapshot
Four New Limonoids from the Barks of Toona ciliata
inferred← citeshttps://doi.org/10.1007/s13659-025-00531-wopenalex-snapshot
Nitrogen-containing secondary metabolites from Meliaceae Family and their biological activity: a review
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Polyketides with potential bioactivities from the mangrove-derived fungus Talaromyces sp. WHUF0362
inferred← citeshttps://doi.org/10.1016/b978-0-08-100017-5.00007-8openalex-snapshot
Five-Membered Ring Systems
inferred← citeshttps://doi.org/10.1016/j.bse.2025.105200openalex-snapshot
Limonoid- and tirucallane-type triterpenoids from the twigs and leaves of Toona ciliata (Meliaceae) and their chemotaxonomic significance
inferred← citeshttps://doi.org/10.1016/j.cclet.2020.09.028openalex-snapshot
Aphamines A–C, dimeric acyclic diterpene enantiomers from Aphanamixis polystachya
inferred← citeshttps://doi.org/10.1016/j.fitote.2013.10.014openalex-snapshot
Chemical constituents from Aphanamixis grandifolia
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104431openalex-snapshot
Two novel nornemoralisin-type diterpenoids from Aphanamixis polystachya (Wall.) R. Parker
inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105192openalex-snapshot
Diverse acyclic diterpene derivatives from Aphanamixis sinensis
inferred← citeshttps://doi.org/10.1016/j.phyplu.2022.100323openalex-snapshot
Identification of phytoconstituents from the aerial parts of Aphanamixis polystachya and evaluation of their anticancer activities
inferred← citeshttps://doi.org/10.1016/j.phytochem.2019.04.008openalex-snapshot
Twelve formyl phloroglucinol meroterpenoids from the leaves of Eucalyptus robusta
inferred← citeshttps://doi.org/10.1016/j.phytol.2013.07.003openalex-snapshot
Ring A rearranged limonoids from the fruits of Aphanamixis grandifolia and their cytotoxicity evaluation
inferred← citeshttps://doi.org/10.1016/j.phytol.2014.02.005openalex-snapshot
New acyclic diterpenoids from the fruits of Aphanamixis grandifolia and structure revision of nemoralisin B
inferred← citeshttps://doi.org/10.1016/j.phytol.2023.08.019openalex-snapshot
New nornemoralisin and nemoralisin diterpenoids from Aphanamixis polystachya
inferred← citeshttps://doi.org/10.1016/j.tet.2014.07.006openalex-snapshot
Diverse prieurianin-type limonoid derivatives from the fruits of Aphanamixis grandifolia and their absolute configuration determination
inferred← citeshttps://doi.org/10.1016/j.tet.2015.02.028openalex-snapshot
Cytotoxic flavonol-diamide [3+2] adducts from the leaves of Aglaia odorata
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00008openalex-snapshot
Synergistic Antifungal Meroterpenes and Dioxolanone Derivatives from the Endophytic Fungus Guignardia sp.
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.9b00787openalex-snapshot
Orthogonal Method for Double-Bond Placement via Ozone-Induced Dissociation Mass Spectrometry (OzID-MS)
inferred← citeshttps://doi.org/10.1021/acs.joc.3c00885openalex-snapshot
Successive Promotion of Formal [3+2] Cycloaddition of Aryl Methyl Ketones by I2 and Zn: Access to 2-Hydroxy-4-morpholin-2,5-diarylfuran-3(2H)-ones with a Quaternary Carbon Center
inferred← citeshttps://doi.org/10.1021/acs.joc.5b00356openalex-snapshot
Copper-Catalyzed [4 + 1] Annulation between α-Hydroxy Ketones and Nitriles: An Approach to Highly Substituted 3(2H)-Furanones
inferred← citeshttps://doi.org/10.1021/jf404726zopenalex-snapshot
Two Novel Anti-Inflammatory 21-Nordammarane Saponins from Tetraploid Jiaogulan (Gynostemma pentaphyllum)
inferred← citeshttps://doi.org/10.1021/jo500318wopenalex-snapshot
Semisynthesis of Libiguin A and Its Analogues by Trans-Lactonization of Phragmalin
inferred← citeshttps://doi.org/10.1021/jo501117kopenalex-snapshot
Total Synthesis of Aphadilactones A–D
inferred← citeshttps://doi.org/10.1021/ol402516popenalex-snapshot
Aphanamenes A and B, Two New Acyclic Diterpene [4 + 2]-Cycloaddition Adducts from Aphanamixis grandifolia
inferred← citeshttps://doi.org/10.1038/s41598-017-13923-xopenalex-snapshot
Small Molecule Accurate Recognition Technology (SMART) to Enhance Natural Products Research
inferred← citeshttps://doi.org/10.1039/c4cc02541eopenalex-snapshot
Broadening the scope of Baeyer–Villiger monooxygenase activities toward α,β-unsaturated ketones: a promising route to chiral enol-lactones and ene-lactones
inferred← citeshttps://doi.org/10.1039/c5ob00674kopenalex-snapshot
Anti-inflammatory diterpene dimers from the root barks of Aphanamixis grandifolia
inferred← citeshttps://doi.org/10.1039/c5ob02296gopenalex-snapshot
Antimalarial diterpenoid dimers of a new carbon skeleton from Aphanamixis grandifolia
inferred← citeshttps://doi.org/10.1039/c8ob02736fopenalex-snapshot
Ciliatasecones A–C, three rearranged limonoids from Toona ciliata var. yunnanensis
inferred← citeshttps://doi.org/10.1039/d0qo01331eopenalex-snapshot
Diverse prieurianin-type limonoids with oxygen-bridged caged skeletons from two Aphanamixis species: discovery and biomimetic conversion
inferred← citeshttps://doi.org/10.1039/d2np00015fopenalex-snapshot
Research progress of meliaceous limonoids from 2011 to 2021
inferred← citeshttps://doi.org/10.1080/10286020.2015.1061511openalex-snapshot
Guanacastane-type diterpenoids from the insect-associated fungus Verticillium dahliae
inferred← citeshttps://doi.org/10.1080/10408398.2022.2033953openalex-snapshot
Minor tropical fruits as a potential source of bioactive and functional foods
inferred← citeshttps://doi.org/10.1080/14786419.2025.2565265openalex-snapshot
Undescribed isoprenoids obtained from Dictamnus dasycarpus Turcz and their cytotoxic activities
inferred← citeshttps://doi.org/10.1080/14786419.2026.2682379openalex-snapshot
Rocaglamides from Aglaia odorata and nemoralisin-type diterpenoids from Aglaia lawii
inferred← citeshttps://doi.org/10.1177/1934578x241302564openalex-snapshot
Phytochemical, Pharmacological and Medicinal Properties of Carapa procera, Trichilia monadelpha, Spathodea campanulata and Gymnosporia senegalensis
inferred← citeshttps://doi.org/10.1360/ssc-2025-0149openalex-snapshot
Progress in the study of non-limonoid natural products of the Meliaceae family
inferred← citeshttps://doi.org/10.2174/1385272827666221017141255openalex-snapshot
Isolation and Bioactivities of Limonoids from Meliaceae Family: A Review
inferred← citeshttps://doi.org/10.26434/chemrxiv-2022-2bpb9-v2openalex-snapshot
Chemistry and Biology of Novel Meliaceae Limonoids
inferred← citeshttps://doi.org/10.26434/chemrxiv-2022-2bpb9-v3openalex-snapshot
Chemistry and Biology of Novel Meliaceae Limonoids
inferred← citeshttps://doi.org/10.3390/molecules27020435openalex-snapshot
The Untargeted Phytochemical Profile of Three Meliaceae Species Related to In Vitro Cytotoxicity and Anti-Virulence Activity against MRSA Isolates
inferred← citeshttps://doi.org/10.3390/molecules27092966openalex-snapshot
Untargeted Metabolomic Approach to Determine the Regulatory Pathways on Salicylic Acid-Mediated Stress Response in Aphanamixis polystachya Seedlings
inferred← citeshttps://doi.org/10.3762/bxiv.2023.47.v1openalex-snapshot
Undescribed triterpenoids obtained from Dictamnus dasycarpus Turcz and their anti-proliferation activities
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