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Putrescine Bisamides from Aglaia gigantea
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/0031-9422(82)85208-4openalex-snapshot
Structure and stereochemistry of (−)-odorinol, an antileukemic diamide from Aglaia odorata
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/s0040-4020(02)00751-2openalex-snapshot
Synthesis and structure elucidation of open-chained putrescine-bisamides from Aglaia species
inferredcites →https://doi.org/10.1016/s0040-4039(01)93688-3openalex-snapshot
Constituents of thai medicinal plants - iv new nitrogenous compounds - odorine and odorinol
inferredcites →https://doi.org/10.1021/ja00011a006openalex-snapshot
High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids
inferredcites →https://doi.org/10.1021/np0102354openalex-snapshot
Rocaglamides, Glycosides, and Putrescine Bisamides from Aglaia dasyclada
inferredcites →https://doi.org/10.1021/np0202475openalex-snapshot
New Chemical Constituents of Euphorbia q uinquecostata and Absolute Configuration Assignment by a Convenient Mosher Ester Procedure Carried Out in NMR Tubes
inferredcites →https://doi.org/10.1021/np50094a004openalex-snapshot
Bisamides from Aglaia Species: Structure Analysis and Potential to Reverse Drug Resistance with Cultured Cells
inferredcites →https://doi.org/10.1021/np9801965openalex-snapshot
Bisamides, Lignans, Triterpenes, and Insecticidal Cyclopenta[b]benzofurans from Aglaia Species
inferredcites →https://doi.org/10.1055/s-2000-9783openalex-snapshot
Phytotoxic Compounds from Xanthocephalum gymnospermoides var. eradiatum1
inferredcites →https://doi.org/10.1127/entom.gen/15/1991/265openalex-snapshot
Contact Toxicity and Feeding Inhibitory Activity of Chromenes from Asteraceae against Spodoptera littoralis (Lepidoptera: Noctuidae)
inferredcites →https://doi.org/10.1248/bpb.24.1282openalex-snapshot
Cancer Chemopreventive Activity of Odorine and Odorinol from Aglaia odorata.
inferredcites →https://doi.org/10.2174/1385272013375049openalex-snapshot
Chemistry and Biological Activity of Rocaglamide Derivatives and Related Compounds in Aglaia Species (Meliaceae)
inferredcites →https://doi.org/10.2174/187152006777698123openalex-snapshot
Potential of Cyclopenta[b]benzofurans from Aglaia Species in Cancer Chemotherapy
inferredcites →https://doi.org/10.7164/antibiotics.57.537openalex-snapshot
Determination of the Absolute Configuration of Synerazol
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/slct.201601639openalex-snapshot
Ni‐Catalyzed Synthesis of Methylenebisamides: Dual Role of DMSO Both as Methylene Source and Oxidant
inferred← citeshttps://doi.org/10.1002/slct.201701081openalex-snapshot
Acryl Activation by Intramolecular Hydrogen Bond: Morita Baylis Hillman Reaction of Acrylamide with Broad Substrate Scope
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/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/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.aihch.2015.04.001openalex-snapshot
De Novo Synthesis of 3-Pyrrolin-2-Ones
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.2022.133184openalex-snapshot
A straightforward synthesis of methylenebisamides from amides and DMSO with a substoichiometric amount of (COCl)2
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.phytol.2015.07.003openalex-snapshot
New bisamide compounds from the bark of Aglaia eximia (Meliaceae)
inferred← citeshttps://doi.org/10.1016/j.tet.2017.08.002openalex-snapshot
Acrylamide in Rauhut-Currier reaction; intramolecular isomerization of activated alkenes for quinolone synthesis
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.01.043openalex-snapshot
Turtschamide, a cytotoxic putrescine bisamide from Corydalis turtschaninovii
inferred← citeshttps://doi.org/10.1021/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/np3007588openalex-snapshot
Bioactive Flavaglines and Other Constituents Isolated from Aglaia perviridis
inferred← citeshttps://doi.org/10.1039/c5ra21801bopenalex-snapshot
Ammonium persulfate activated DMSO as a one-carbon synthon for the synthesis of methylenebisamides and other applications
inferred← citeshttps://doi.org/10.1055/s-0039-1690031openalex-snapshot
DMSO-Mediated Synthesis of Methylene-Bridged Unsymmetrical Bisamides in the Presence of AcOH
inferred← citeshttps://doi.org/10.1139/cjc-2018-0181openalex-snapshot
Selectfluor-mediated oxidative methylenation of amide with N,N-dimethylpropanamide for N,N′-methylenebisamide synthesis
inferred← citeshttps://doi.org/10.1248/cpb.58.1116openalex-snapshot
Cucullamide, a New Putrescine Bisamide from Amoora cucullata
inferred← citeshttps://doi.org/10.22146/ijc.64502openalex-snapshot
Phytochemistry and Pharmacology of Munronia Genus (Meliaceae)
inferred← citeshttps://doi.org/10.3762/bjoc.10.9openalex-snapshot
Total synthesis of (+)-grandiamide D, dasyclamide and gigantamide A from a Baylis–Hillman adduct: A unified biomimetic approach
inferred← citeshttps://doi.org/10.4172/2161-0444.1000167openalex-snapshot
Synthesis of Putrescine Bisamides as Antimicrobial and Anti-Inflammatory Agents
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