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Rocaglamides, Glycosides, and Putrescine Bisamides from Aglaia dasyclada

https://doi.org/10.1021/np0102354
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1016/0040-4020(96)00322-5openalex-snapshot
New nitrogenous and aromatic derivatives from Aglaia argentea and A. forbesii
inferredcites →https://doi.org/10.1016/s0031-9422(00)00205-3openalex-snapshot
Insecticidal rocaglamide derivatives from Aglaia spectabilis (Meliaceae)
inferredcites →https://doi.org/10.1016/s0031-9422(00)94986-0openalex-snapshot
Insecticidal 1H-cyclopentatetrahydro[b]benzofurans from Aglaia odorata
inferredcites →https://doi.org/10.1016/s0031-9422(96)00763-7openalex-snapshot
Insecticidal rocaglamide derivatives from Aglaia duppereana
inferredcites →https://doi.org/10.1016/s0031-9422(97)00253-7openalex-snapshot
Insecticidal rocaglamide derivatives from Aglaia elliptica and A. harmsiana
inferredcites →https://doi.org/10.1016/s0031-9422(98)00751-1openalex-snapshot
An insecticidal rocaglamide derivatives and related compounds from Aglaia odorata (Meliaceae)
inferredcites →https://doi.org/10.1016/s0031-9422(99)00185-5openalex-snapshot
Thapsakins: possible biogenetic intermediates towards insecticidal cyclopenta[b]benzofurans from Aglaia edulis
inferredcites →https://doi.org/10.1016/s0031-9422(99)00327-1openalex-snapshot
New insecticidal rocaglamide derivatives from flowers of Aglaia duperreana (Meliaceae)
inferredcites →https://doi.org/10.1016/s0031-9422(99)00519-1openalex-snapshot
Three putrescine bisamides from the leaves of Aglaia grandis
inferredcites →https://doi.org/10.1021/np9801965openalex-snapshot
Bisamides, Lignans, Triterpenes, and Insecticidal Cyclopenta[b]benzofurans from Aglaia Species
inferredcites →https://doi.org/10.1021/np990242gopenalex-snapshot
New Insecticidal Rocaglamide Derivatives from the Roots of Aglaia duperreana

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.2020.112540zenodo-depositor-declared
Phytochemistry and biological activities of Aglaia species
inferred← citeshttps://doi.org/10.1002/cbdv.202101008openalex-snapshot
Three New Aglain Derivatives from Aglaia odorata Lour. and Their Cytotoxic Activities
inferred← citeshttps://doi.org/10.1002/slct.201601639openalex-snapshot
Ni‐Catalyzed Synthesis of Methylenebisamides: Dual Role of DMSO Both as Methylene Source and Oxidant
inferred← citeshttps://doi.org/10.1002/vjch.202400102openalex-snapshot
The genus Aglaia: Diversity in chemical structure and biological activity
inferred← citeshttps://doi.org/10.1007/978-3-7091-0748-5_1openalex-snapshot
Chemistry and Biology of Rocaglamides (= Flavaglines) and Related Derivatives from Aglaia Species (Meliaceae)
inferred← citeshttps://doi.org/10.1007/s10600-019-02656-0openalex-snapshot
Chromone Alkaloids: Structural Features, Distribution in Nature, and Biological Activity
inferred← citeshttps://doi.org/10.1007/s11101-021-09761-5openalex-snapshot
Comparative phytochemistry of flavaglines (= rocaglamides), a group of highly bioactive flavolignans from Aglaia species (Meliaceae)
inferred← citeshttps://doi.org/10.1007/s12272-026-01613-0openalex-snapshot
Glycosides in Meliaceae and Rutaceae sources: phytochemistry and pharmacological activities
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/bs.alkal.2016.04.001openalex-snapshot
Flavoalkaloids—Isolation, Biological Activity, and Total Synthesis
inferred← citeshttps://doi.org/10.1016/j.bjp.2014.11.009openalex-snapshot
Phytochemicals and antimicrobial potentials of mahogany family
inferred← citeshttps://doi.org/10.1016/j.bse.2011.12.022openalex-snapshot
Chemical constituents from Aglaia odorata Lour
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.141472openalex-snapshot
Iron-catalyzed direct N-methylation of N‑methoxy benzamides: A solvent-free approach to bisamides utilizing the methoxy group as a “build-in” methylene donor
inferred← citeshttps://doi.org/10.1016/j.phytochem.2007.10.015openalex-snapshot
Amide-esters from Aglaia tenuicaulis – First representatives of a class of compounds structurally related to bisamides and flavaglines
inferred← citeshttps://doi.org/10.1016/j.tet.2015.04.030openalex-snapshot
Rhodium-catalyzed asymmetric intramolecular addition of arylboronic acids to ketones: catalytic enantioselective access to 3-hydroxy-2,3-dihydrobenzofurans bearing a tetrasubstituted carbon stereocenter
inferred← citeshttps://doi.org/10.1016/j.tet.2020.131257openalex-snapshot
Anti-inflammatory flavagline glycosides and putrescine bisamides from Aglaia perviridis leaves
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.01.043openalex-snapshot
Turtschamide, a cytotoxic putrescine bisamide from Corydalis turtschaninovii
inferred← citeshttps://doi.org/10.1016/s0040-4020(02)00014-5openalex-snapshot
A novel tandem reaction of 3-substituted coumarins with two equivalents of dimethylsulfoxonium ylide to 2-substituted cyclopenta[b]benzofuran-3-ol derivatives
inferred← citeshttps://doi.org/10.1016/s0040-4039(02)01180-2openalex-snapshot
New methoxylated aryltetrahydronaphthalene lignans and a norlignan from Aglaia cordata
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c00646openalex-snapshot
Visible-Light-Induced Radical Cascade Cross-Coupling via C(sp3)–H Activation and C–N/N–O Cleavage: Feasible Access to Methylenebisamide Derivatives
inferred← citeshttps://doi.org/10.1021/jo040120fopenalex-snapshot
Silvestrol and Episilvestrol, Potential Anticancer Rocaglate Derivatives from Aglaia silvestris
inferred← citeshttps://doi.org/10.1021/np0304417openalex-snapshot
Cytotoxic Constituents of the Twigs and Leaves ofAglaiarubiginosa
inferred← citeshttps://doi.org/10.1021/np034057lopenalex-snapshot
Aglacins I−K, Three Highly Methoxylated Lignans from Aglaia cordata
inferred← citeshttps://doi.org/10.1021/np060428xopenalex-snapshot
Cytotoxic Flavaglines and Bisamides from Aglaia edulis
inferred← citeshttps://doi.org/10.1021/np070184wopenalex-snapshot
Putrescine Bisamides from Aglaia gigantea
inferred← citeshttps://doi.org/10.1021/np3007588openalex-snapshot
Bioactive Flavaglines and Other Constituents Isolated from Aglaia perviridis
inferred← citeshttps://doi.org/10.1039/c004927aopenalex-snapshot
Constituents of Amoora cucullata with TRAIL resistance-overcoming activity
inferred← citeshttps://doi.org/10.1080/10286020.2015.1057575openalex-snapshot
Two new lignans from twigs of Aglaia odorata
inferred← citeshttps://doi.org/10.1080/14786419.2022.2114472openalex-snapshot
New dammarane-type triterpenoids from Aglaia elliptica (C.DC.) blume
inferred← citeshttps://doi.org/10.1248/cpb.54.1344openalex-snapshot
Potent Cytotoxic Rocaglamide Derivatives from the Fruits of Amoora cucullata
inferred← citeshttps://doi.org/10.1248/cpb.58.1116openalex-snapshot
Cucullamide, a New Putrescine Bisamide from Amoora cucullata
inferred← citeshttps://doi.org/10.1248/cpb.c15-00732openalex-snapshot
Bio-active Natural Products with TRAIL-Resistance Overcoming Activity
inferred← citeshttps://doi.org/10.20884/1.jm.2017.12.2.361openalex-snapshot
A Cytotoxic Rocaglate Compound from The Stembark of Aglaia argentea (Meliaceae)
inferred← citeshttps://doi.org/10.2147/bctt.s429721openalex-snapshot
Evaluation of Cytotoxicity of the Methanolic Extract of Red Sea Marine Sponge Xestospongia Testudinaria and Its Related Compounds Against MCF-7 Human Breast Cancer Cells
inferred← citeshttps://doi.org/10.7454/mss.v19i1.4476openalex-snapshot
Flavonoid Compounds from the Bark of Aglaia eximia (Meliaceae)
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