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Total Synthesis of the Potent Anticancer Aglaia Metabolites (−)-Silvestrol and (−)-Episilvestrol and the Active Analogue (−)-4′-Desmethoxyepisilvestrol
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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.198201553openalex-snapshot
Advances in Selective Chemical Syntheses of Complex Oligosaccharides
inferredcites →https://doi.org/10.1002/anie.200462172openalex-snapshot
Cu(OTf)2 as an Efficient and Dual‐Purpose Catalyst in the Regioselective Reductive Ring Opening of Benzylidene Acetals
inferredcites →https://doi.org/10.1002/anie.200702700openalex-snapshot
Total Synthesis of (−)‐Episilvestrol and (−)‐Silvestrol
inferredcites →https://doi.org/10.1002/anie.200702707openalex-snapshot
Enantioselective Synthesis of the Complex Rocaglate (−)‐Silvestrol
inferredcites →https://doi.org/10.1002/ejoc.200400891openalex-snapshot
A Highly Efficient Synthesis of Rocaglaols by a Novel α‐Arylation of Ketones
inferredcites →https://doi.org/10.1002/jccs.200100097openalex-snapshot
The Host/Guest Type of Excited‐State Proton Transfer; a General Review
inferredcites →https://doi.org/10.1002/prac.19983400305openalex-snapshot
Structure and Reactions of Glycopyranoside Derived Dialdehydes
inferredcites →https://doi.org/10.1016/0014-2999(92)90156-xopenalex-snapshot
PAF antagonism in vitro and in vivo by aglafoline from Aglaia elliptifolia Merr
inferredcites →https://doi.org/10.1016/j.tetlet.2004.11.057openalex-snapshot
Biomimetic synthesis of the novel 1,4-dioxanyloxy fragment of silvestrol and episilvestrol
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(98)00751-1openalex-snapshot
An insecticidal rocaglamide derivatives and related compounds from Aglaia odorata (Meliaceae)
inferredcites →https://doi.org/10.1016/s0040-4020(98)01015-1openalex-snapshot
Unprecedented concentration dependent chemical shift variation in1H-NMR studies: A caveat in the investigations of molecular recognition and structure elucidation
inferredcites →https://doi.org/10.1016/s0040-4039(00)00021-6openalex-snapshot
A new analogue of rocaglamide by an oxidative dihydrofuran synthesis
inferredcites →https://doi.org/10.1016/s0040-4039(00)73983-9openalex-snapshot
A biomimetic approach to the synthesis of rocaglamide based on a photochemical [2+2] cycloaddition of a cinnamate unit to a flavone.
inferredcites →https://doi.org/10.1016/s0040-4039(01)01807-xopenalex-snapshot
Total synthesis of (±)-rocaglamide and some aryl analogues
inferredcites →https://doi.org/10.1016/s0040-4039(99)00706-6openalex-snapshot
Synthesis of the carbocyclic analogue of (±)-Rocaglamide
inferredcites →https://doi.org/10.1021/ja00113a013openalex-snapshot
Studies on the Synthesis of Aureolic Acid Antibiotics: Highly Stereoselective Synthesis of Aryl 2-Deoxy-.beta.-glycosides via the Mitsunobu Reaction and Synthesis of the Olivomycin A-B Disaccharide
inferredcites →https://doi.org/10.1021/ja00180a081openalex-snapshot
An unusual oxidative cyclization. A synthesis and absolute stereochemical assignment of (-)-rocaglamide
inferredcites →https://doi.org/10.1021/ja00219a035openalex-snapshot
Directed reduction of .beta.-hydroxy ketones employing tetramethylammonium triacetoxyborohydride
inferredcites →https://doi.org/10.1021/ja044798oopenalex-snapshot
A Biomimetic Approach to the Rocaglamides Employing Photogeneration of Oxidopyryliums Derived from 3-Hydroxyflavones
inferredcites →https://doi.org/10.1021/ja062621jopenalex-snapshot
Enantioselective Photocycloaddition Mediated by Chiral Brønsted Acids: Asymmetric Synthesis of the Rocaglamides
inferredcites →https://doi.org/10.1021/ja993366oopenalex-snapshot
Stereochemical Reversal of Nucleophilic Substitution Reactions Depending upon Substituent: Reactions of Heteroatom-Substituted Six-Membered-Ring Oxocarbenium Ions through Pseudoaxial Conformers
inferredcites →https://doi.org/10.1021/jo00015a008openalex-snapshot
Radical-mediated intramolecular [3-atom + 2-atom] addition and the synthesis of (.+-.)-rocaglamide: model studies
inferredcites →https://doi.org/10.1021/jo00020a003openalex-snapshot
A highly stereoselective synthesis of aryl 2-deoxy-.beta.-glycosides via the Mitsunobu reaction
inferredcites →https://doi.org/10.1021/jo00026a020openalex-snapshot
Epoxidation of flavones by dimethyldioxirane
inferredcites →https://doi.org/10.1021/jo00211a029openalex-snapshot
Diels-Alder approach to bicyclic .alpha.-hydroxy ketones. Facile ketol rearrangements of strained .alpha.-hydroxy ketones
inferredcites →https://doi.org/10.1021/jo00262a022openalex-snapshot
A synthetic approach to rocaglamide via reductive cyclization of .delta.-keto nitriles
inferredcites →https://doi.org/10.1021/jo01311a040openalex-snapshot
Epoxidation of alkenes by dioxirane intermediates generated in the reaction of potassium caroate with ketones
inferredcites →https://doi.org/10.1021/jo040008hopenalex-snapshot
Silvestrol and Episilvestrol, Potential Anticancer Rocaglate Derivatives from Aglaia silvestris.
inferredcites →https://doi.org/10.1021/jo040120fopenalex-snapshot
Silvestrol and Episilvestrol, Potential Anticancer Rocaglate Derivatives from Aglaia silvestris
inferredcites →https://doi.org/10.1021/jp013840oopenalex-snapshot
Proton Transfer in 3-Hydroxyflavone Studied by High-Resolution 10 K Laser-Excited Shpol'skii Spectroscopy
inferredcites →https://doi.org/10.1021/np970163+openalex-snapshot
Cytotoxic and Antiplatelet Aggregation Principles from Aglaia elliptifolia
inferredcites →https://doi.org/10.1021/ol0479904openalex-snapshot
Stereoselective Synthesis of (±)-Rocaglaol Analogues
inferredcites →https://doi.org/10.1021/ol0513793openalex-snapshot
Stereospecific Synthesis of (±)-1,2-Anhydro Methyl Rocaglate
inferredcites →https://doi.org/10.1021/ol801435jopenalex-snapshot
Stereoselective Synthesis of the Rocaglamide Skeleton via a Silyl Vinylketene Formation/[4 + 1] Annulation Sequence
inferredcites →https://doi.org/10.1039/c39820001150openalex-snapshot
X-Ray crystal structure of rocaglamide, a novel antileulemic 1H-cyclopenta[b]benzofuran from Aglaia elliptifolia
inferredcites →https://doi.org/10.1039/c39870000025openalex-snapshot
A novel 1,3-dithiane-based cyclopenta-annellation procedure: synthesis of the rocaglamide skeleton
inferredcites →https://doi.org/10.1039/p19850000799openalex-snapshot
Lithiation in flavones, chromones, coumarins, and benzofuran derivatives
inferredcites →https://doi.org/10.1039/p19920002657openalex-snapshot
Synthesis of the novel anti-leukaemic tetrahydrocyclopenta[b]benzofuran, rocaglamide and related synthetic studies
inferredcites →https://doi.org/10.1039/p29820000071openalex-snapshot
n-π Interaction between an oxygen lone pair and π-electrons in cyclic allylic alcohols and ethers; carbon-13 nuclear magnetic resonance spectra, catalytic hydrogenation, and CNDO/2 calculations
inferredcites →https://doi.org/10.1055/s-1981-29317openalex-snapshot
The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products
inferredcites →https://doi.org/10.1055/s-1999-2771openalex-snapshot
Sequential Anionic 1,3 Ester Shifts and Intramolecular Stille Couplings: A New Protocol for the Concise Assembly of Functionalized Polycyclic Dienes
inferredcites →https://doi.org/10.1080/07328308408057898openalex-snapshot
1-O-Alkylation of D-Glucopyranose
inferredcites →https://doi.org/10.1246/bcsj.68.2401openalex-snapshot
A Practical Synthesis of Mannosaminyl-β(1→4)-glucosyl-α(1→2)-rhamnose, the Trisaccharide Repeating Unit of a Streptococcus pneumoniae Capsular Polysaccharide
inferredcites →https://doi.org/10.1246/cl.1992.707openalex-snapshot
A Practical, Highly Stereoselective Synthesis of the Trisaccharide Repeating Unit of a Streptococcus pneumoniae Polysaccharide
inferredcites →https://doi.org/10.1246/cl.2007.566openalex-snapshot
Di-2-methoxyethyl Azodicarboxylate (DMEAD): An Inexpensive and Separation-friendly Alternative Reagent for the Mitsunobu Reaction
inferredcites →https://doi.org/10.2174/1385272013375049openalex-snapshot
Chemistry and Biological Activity of Rocaglamide Derivatives and Related Compounds in Aglaia Species (Meliaceae)
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/ange.201002845openalex-snapshot
Photochemische Reaktionen als Schlüsselschritte in der Naturstoffsynthese
inferred← citeshttps://doi.org/10.1002/ange.201003212openalex-snapshot
Biomimetic Photocycloaddition of 3‐Hydroxyflavones: Synthesis and Evaluation of Rocaglate Derivatives as Inhibitors of Eukaryotic Translation
inferred← citeshttps://doi.org/10.1002/ange.201501374openalex-snapshot
Synthesis of Each Enantiomer of Rocaglamide by Means of a Palladium(0)‐Catalyzed Nazarov‐Type Cyclization
inferred← citeshttps://doi.org/10.1002/anie.201002845openalex-snapshot
Photochemical Reactions as Key Steps in Natural Product Synthesis
inferred← citeshttps://doi.org/10.1002/anie.201003212openalex-snapshot
Biomimetic Photocycloaddition of 3‐Hydroxyflavones: Synthesis and Evaluation of Rocaglate Derivatives as Inhibitors of Eukaryotic Translation
inferred← citeshttps://doi.org/10.1002/anie.201501374openalex-snapshot
Synthesis of Each Enantiomer of Rocaglamide by Means of a Palladium(0)‐Catalyzed Nazarov‐Type Cyclization
inferred← citeshttps://doi.org/10.1002/aoc.4464openalex-snapshot
Applications of Mitsunobu Reaction in total synthesis of natural products
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Installation of Amine Moieties into a Polycyclic Anodic Product Derived from 2,4‐Dimethylphenol
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Total Synthesis of the Antiviral Natural Product Houttuynoid B
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The Evolution of the Total Synthesis of Rocaglamide
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Simplified Silvestrol Analogues with Potent Cytotoxic Activity
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Reduction of Alkynyl α‐Hydroxy Esters: Stereoselective α‐Ketol Rearrangement
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Recent Advances in the Synthesis of Flavaglines, a Family of Potent Bioactive Natural Compounds Originating from Traditional Chinese Medicine
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The Search for Anticancer Agents from Tropical Plants
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Chemistry and Biology of Rocaglamides (= Flavaglines) and Related Derivatives from Aglaia Species (Meliaceae)
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Comparative phytochemistry of flavaglines (= rocaglamides), a group of highly bioactive flavolignans from Aglaia species (Meliaceae)
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Five-Membered Ring Systems: Furans and Benzofurans
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Five-Membered Ring Systems
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5.08 Thermal and Metal-Induced [3+2] Cycloadditions
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The rocaglate CR-31-B (−) inhibits SARS-CoV-2 replication at non-cytotoxic, low nanomolar concentrations in vitro and ex vivo
inferred← citeshttps://doi.org/10.1016/j.biopha.2024.117047openalex-snapshot
Silvestrol, a potent anticancer agent with unfavourable pharmacokinetics: Current knowledge on its pharmacological properties and future directions for the development of novel drugs
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Recent advances in the biology and chemistry of the flavaglines
inferred← citeshttps://doi.org/10.1016/j.bmcl.2015.12.045openalex-snapshot
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Five-Membered Ring Systems
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Structurally Modified Cyclopenta[b]benzofuran Analogues Isolated from Aglaia perviridis
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inferred← citeshttps://doi.org/10.1021/np3007588openalex-snapshot
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The novel plant-derived agent silvestrol has B-cell selective activity in chronic lymphocytic leukemia and acute lymphoblastic leukemia in vitro and in vivo
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Photochemical Key Steps in Organic Synthesis
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Naturally Occurring O-Heterocycles as Anticancer Agents
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Inhibitors of Translation Initiation as Cancer Therapeutics
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Synthèse de nouveaux agents anticancéreux
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