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Turrapubesins A and B, First Examples of Halogenated and Maleimide-Bearing Limonoids in Nature from Turraea pubescens
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-3-662-04201-4openalex-snapshot
Structure Determination of Organic Compounds
inferredcites →https://doi.org/10.1016/0031-9422(92)90003-9openalex-snapshot
Biological activity of limonoids from the rutales
inferredcites →https://doi.org/10.1016/0031-9422(96)00276-2openalex-snapshot
2-Ethyl-3-methylmaleimide N-β-d-glucopyranoside from the leaves of mangosteen (Garcinia mangostana)
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.2004.06.019openalex-snapshot
Limonoids from Turraea floribunda (Meliaceae)
inferredcites →https://doi.org/10.1016/j.phytochem.2005.02.017openalex-snapshot
Secondary metabolites of slime molds (myxomycetes)
inferredcites →https://doi.org/10.1016/s0031-9422(03)00028-1openalex-snapshot
Tetranortriterpenoid derivatives from Turraea parvifolia (Meliaceae)
inferredcites →https://doi.org/10.1016/s0305-1978(03)00034-6openalex-snapshot
Limonoids from Turraea parvifolia (Meliaceae)
inferredcites →https://doi.org/10.1021/ja00339a031openalex-snapshot
Additivity relation in the amplitudes of exciton-split circular dichroism curves arising from interactions between different chromophores and its application in structural studies
inferredcites →https://doi.org/10.1021/ja00339a032openalex-snapshot
Crown thiaether chemistry. Crystal structure of 1,4,7,10,13,16-hexathiacyclooctadecane, the hexathia analog of 18-crown-6
inferredcites →https://doi.org/10.1021/ja00408a062openalex-snapshot
Additivity relation found in the amplitudes of exciton-split circular dichroism curves of pyranose benzoates
inferredcites →https://doi.org/10.1021/ja00782a043openalex-snapshot
Absolute configuration of natural (+)-abscisic acid
inferredcites →https://doi.org/10.1021/ja00782a044openalex-snapshot
Absolute configuration of (+)-trans-abscisic acid as determined by a quantitative application of the exciton chirality method
inferredcites →https://doi.org/10.1021/jf049474yopenalex-snapshot
New Mosquito Larvicidal Tetranortriterpenoids from Turraea wakefieldii and Turraea floribunda
inferredcites →https://doi.org/10.1021/jo961789sopenalex-snapshot
Didemnimides A−D: Novel, Predator-Deterrent Alkaloids from the Caribbean Mangrove Ascidian Didemnum conchyliatum
inferredcites →https://doi.org/10.1021/np030293kopenalex-snapshot
Five New Maleic and Succinic Acid Derivatives from the Mycelium of Antrodia c amphorata and Their Cytotoxic Effects on LLC Tumor Cell Line
inferredcites →https://doi.org/10.1021/np980409qopenalex-snapshot
A Cyclized Didemnimide Alkaloid from the Caribbean Ascidian Didemnum conchyliatum
inferredcites →https://doi.org/10.1093/jnci/82.13.1107openalex-snapshot
New Colorimetric Cytotoxicity Assay for Anticancer-Drug Screening
inferredcites →https://doi.org/10.1107/s0108767383001762openalex-snapshot
On enantiomorph-polarity estimation
inferredcites →https://doi.org/10.2174/1385272003375941openalex-snapshot
The Chemistry of the Meliaceae and Ptaeroxylaceae of Southern and Eastern Africa and Madagascar
inferredcites →https://doi.org/10.7164/antibiotics.53.765openalex-snapshot
TAN-1813, a Novel Ras-Farnesyltransferase Inhibitor Produced by Phoma sp. Taxonomy, Fermentation, Isolation and Biological Activities In Vitro and In Vivo.
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.2021.112661zenodo-depositor-declared
Toonaones A−I, limonoids with NLRP3 inflammasome inhibitory activity from Toona ciliata M. Roem
inferred← citeshttps://doi.org/10.1002/chin.200701180openalex-snapshot
Turrapubesins A (I) and B (II), First Examples of Halogenated and Maleimide‐Bearing Limonoids in Nature from Turraea pubescens.
inferred← citeshttps://doi.org/10.1002/hlca.200890055openalex-snapshot
Cytotoxic Terpenoids from Turraea pubescens
inferred← citeshttps://doi.org/10.1002/hlca.200890254openalex-snapshot
Limonoids from the Twigs and Leaves of Chukrasia tabularis
inferred← citeshttps://doi.org/10.1007/978-981-99-7329-3_6openalex-snapshot
Classification of Diverse Novel Limonoids
inferred← citeshttps://doi.org/10.1007/s11224-011-9818-8openalex-snapshot
Spectroscopic characterizations, X-ray studies, and electronic circular dichroism calculations of two alkaloid triterpenoids
inferred← citeshttps://doi.org/10.1007/s11427-020-1799-yopenalex-snapshot
Natural product sciences: an integrative approach to the innovations of plant natural products
inferred← citeshttps://doi.org/10.1007/s13659-025-00531-wopenalex-snapshot
Nitrogen-containing secondary metabolites from Meliaceae Family and their biological activity: a review
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.11428-3openalex-snapshot
Oxiranes and Oxirenes: Fused-ring Derivatives☆
inferred← citeshttps://doi.org/10.1016/b978-008044992-0.00104-8openalex-snapshot
Oxiranes and Oxirenes: Fused-ring Derivatives
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104363openalex-snapshot
Toonaolides A–X, limonoids from Toona ciliata: Isolation, structural elucidation, and bioactivity against NLRP3 inflammasome
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.2019.104244openalex-snapshot
Phenolic cyclobutantetraol esters from Scindapsus officinalis (Roxb.) Schott
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104294openalex-snapshot
New eremophilane-type sesquiterpenes and maleimide-bearing compounds from Carpesium abrotanoides L.
inferred← citeshttps://doi.org/10.1016/j.foodchem.2011.09.021openalex-snapshot
Biological activities of flavonoids from pathogenic-infected Astragalus adsurgens
inferred← citeshttps://doi.org/10.1016/j.indcrop.2020.112275openalex-snapshot
Diverse limonoids from barks of Toona ciliata var. yunnanensis and their biological activities
inferred← citeshttps://doi.org/10.1016/j.indcrop.2021.113533openalex-snapshot
The bioactive limonoids from Toona ciliate as NLRP3 inflammasome inhibitors
inferred← citeshttps://doi.org/10.1016/j.phytochem.2008.01.018openalex-snapshot
Structural elucidation of limonoids and steroids from Trichilia connaroides
inferred← citeshttps://doi.org/10.1016/j.phytochem.2010.06.010openalex-snapshot
Mulavanins A–E: Limonoids from Munronia delavayi
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112282openalex-snapshot
Highly oxygenated and rearranged limonoids from the stem barks of Entandrophragma utile
inferred← citeshttps://doi.org/10.1016/j.tet.2007.05.107openalex-snapshot
Eight new limonoids from Turraea pubescens
inferred← citeshttps://doi.org/10.1016/j.tet.2015.09.025openalex-snapshot
B-seco-29-nor-Limonoids from the stem barks of Toona ciliate var. yunnanensis
inferred← citeshttps://doi.org/10.1016/j.tet.2016.09.061openalex-snapshot
Limonoids with modified furan rings from root barks of Toona sinensis
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.08.066openalex-snapshot
Swiemahogins A and B, two novel limonoids from Swietenia mahogani
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.10.055openalex-snapshot
Two rare limonoids from the stem barks of Entandrophragma utile
inferred← citeshttps://doi.org/10.1016/s1875-5364(09)60008-xopenalex-snapshot
Natural Products Chemistry Research 2006's Progress in China
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.4c00313openalex-snapshot
Isolation, Characterization, and Antiproliferative Activity of Terpenoids from the Tropical Plant Turraea delphinensis
inferred← citeshttps://doi.org/10.1021/cr9004023openalex-snapshot
Meliaceous Limonoids: Chemistry and Biological Activities
inferred← citeshttps://doi.org/10.1021/jf3049774openalex-snapshot
Limonoids from the Fruits of Aphanamixis polystachya (Meliaceae) and Their Biological Activities
inferred← citeshttps://doi.org/10.1021/np070345wopenalex-snapshot
Nortriterpenoids from Chukrasia tabularis var. velutina
inferred← citeshttps://doi.org/10.1021/np070476xopenalex-snapshot
Limonoids and Sesquiterpenoids from Amoora tsangii
inferred← citeshttps://doi.org/10.1021/np100150nopenalex-snapshot
Mesendanins A−J, Limonoids from the Leaves and Twigs of Melia toosendan
inferred← citeshttps://doi.org/10.1021/np100307fopenalex-snapshot
Tirucallane-Type Alkaloids from the Bark of Dysoxylum laxiracemosum
inferred← citeshttps://doi.org/10.1021/np400276qopenalex-snapshot
Bioactive Limonoid and Triterpenoid Constituents of Turraea pubescens
inferred← citeshttps://doi.org/10.1021/np401089hopenalex-snapshot
C-17 Lactam-Bearing Limonoids from the Twigs and Leaves of Amoora tsangii
inferred← citeshttps://doi.org/10.1021/np800242wopenalex-snapshot
Cadinane Sesquiterpenes from the Leaves of Eupatorium adenophorum
inferred← citeshttps://doi.org/10.1021/np9002806openalex-snapshot
Farinomalein, a Maleimide-Bearing Compound from the Entomopathogenic Fungus Paecilomyces farinosus
inferred← citeshttps://doi.org/10.1021/ol3008149openalex-snapshot
Aphanamixoid A, a Potent Defensive Limonoid, with a New Carbon Skeleton from Aphanamixis polystachya
inferred← citeshttps://doi.org/10.1021/ol400875nopenalex-snapshot
Two New Highly Oxygenated and Rearranged Limonoids from Phyllanthus cochinchinensis
inferred← citeshttps://doi.org/10.1021/ol402318mopenalex-snapshot
Laevinoids A and B: Two Diterpenoids with an Unprecedented Backbone from Croton laevigatus
inferred← citeshttps://doi.org/10.1021/ol800415nopenalex-snapshot
Cipadonoid A, a Novel Limonoid with an Unprecedented Skeleton, from Cipadessa cinerasecns
inferred← citeshttps://doi.org/10.1021/ol800885hopenalex-snapshot
Chuktabrins A and B, Two Novel Limonoids from the Twigs and Leaves of Chukrasia tabularis
inferred← citeshttps://doi.org/10.1021/ol802678sopenalex-snapshot
Two Limonoids, Khayalenoids A and B with an Unprecedented 8-Oxa-tricyclo[4.3.2.02,7]undecane Motif, from Khaya senegalensis
inferred← citeshttps://doi.org/10.1021/ol902565sopenalex-snapshot
Structure Determination of Grandifotane A from Khaya grandifoliola by NMR, X-ray Diffraction, and ECD Calculation
inferred← citeshttps://doi.org/10.1038/aps.2012.105openalex-snapshot
Discovery of structurally diverse and bioactive compounds from plant resources in China
inferred← citeshttps://doi.org/10.1039/c7qo00678kopenalex-snapshot
Rearranged limonoids with unique 6/5/6/5 tetracarbocyclic skeletons from Toona ciliata and biomimetic structure divergence
inferred← citeshttps://doi.org/10.1039/d1ce01488aopenalex-snapshot
High temperature molecular-based phase transition compounds with tunable and switchable dielectric properties
inferred← citeshttps://doi.org/10.1080/00032719.2017.1327536openalex-snapshot
Fragmentation Study of Limonoids from Turraae pubescens by Electrospray Ionization Quadrupole Time-of-flight Mass Spectrometry
inferred← citeshttps://doi.org/10.1248/cpb.59.1003openalex-snapshot
Limonoids and Triterpenoids from the Seeds of Melia azedarach
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/10.3762/bjoc.10.15openalex-snapshot
Synthesis of the B-seco limonoid core scaffold
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