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Palladium(II)-Catalyzed Cyclization of Unsaturated Hydroperoxides for the Synthesis of 1,2-Dioxanes
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Efficient Intramolecular Oxidative Amination of Olefins through Direct Dioxygen-Coupled Palladium Catalysis
inferredcites →https://doi.org/10.1002/anie.198207341openalex-snapshot
Oxygen Transfer from Inorganic and Organic Peroxides to Organic Substrates: A Common Mechanism?
inferredcites →https://doi.org/10.1002/anie.200460060openalex-snapshot
Palladium‐Catalyzed Synthesis of N ‐Aryl Pyrrolidines from γ‐( N ‐Arylamino) Alkenes: Evidence for Chemoselective Alkene Insertion into PdN Bonds
inferredcites →https://doi.org/10.1002/anie.200603954openalex-snapshot
Electrophilic Activation of Alkenes by Platinum(II): So Much More Than a Slow Version of Palladium(II)
inferredcites →https://doi.org/10.1002/anie.200802187openalex-snapshot
Synthesis of Indolines and Tetrahydroisoquinolines from Arylethylamines by Pd II ‐Catalyzed CH Activation Reactions
inferredcites →https://doi.org/10.1002/chin.200512123openalex-snapshot
Palladium‐Catalyzed Synthesis of N‐Aryl‐2‐benzylindolines via Tandem Arylation of 2‐Allylaniline: Control of Selectivity Through in situ Catalyst Modification.
inferredcites →https://doi.org/10.1002/med.10066openalex-snapshot
Synthetic peroxides as antimalarials
inferredcites →https://doi.org/10.1007/s00280-003-0751-4openalex-snapshot
Antimalarial dihydroartemisinin also inhibits angiogenesis
inferredcites →https://doi.org/10.1016/0040-4020(95)00793-8openalex-snapshot
Two Cytotoxic 3,6-Epidioxy Fatty Acids from an Indonesian Sponge, Plakortis sp. 1
inferredcites →https://doi.org/10.1016/0040-4039(95)00714-nopenalex-snapshot
Concise synthesis of yingzhaosu C and epi-yingzhaosu C by peroxyl radical cyclization. Assignment of relative configuration
inferredcites →https://doi.org/10.1016/0040-4039(95)02199-xopenalex-snapshot
Synthesis of 1,2-dioxanes, 1,2,4-trioxanes, and 1,2,4-trioxepanes via cyclizations of unsaturated hydroperoxyacetals
inferredcites →https://doi.org/10.1016/j.bmcl.2007.04.054openalex-snapshot
A novel artemisinin–quinine hybrid with potent antimalarial activity
inferredcites →https://doi.org/10.1016/j.bmcl.2008.10.083openalex-snapshot
Synthesis of spiro-1,2-dioxolanes and their activity against Plasmodium falciparum
inferredcites →https://doi.org/10.1016/j.drup.2005.04.003openalex-snapshot
Mechanistic perspectives for 1,2,4-trioxanes in anti-cancer therapy
inferredcites →https://doi.org/10.1016/j.ejmech.2007.04.019openalex-snapshot
Bioactive peroxides as potential therapeutic agents
inferredcites →https://doi.org/10.1016/j.jorganchem.2006.05.059openalex-snapshot
Ruthenium-catalyzed intramolecular cyclization of hetero-functionalized allylbenzenes
inferredcites →https://doi.org/10.1016/s0040-4039(00)81459-8openalex-snapshot
Intramolecular alkylation of peroxides and hydroperoxides; peroxide transfer via peroxonium intermediates
inferredcites →https://doi.org/10.1016/s0040-4039(00)95228-6openalex-snapshot
Ozonolysis; intramolecular trapping of the “Criegee intermediate”. X-Ray analysis and anomeric effect in a 6-hydroxy-3-methoxy-1,2-dioxane
inferredcites →https://doi.org/10.1016/s0040-4039(01)01493-9openalex-snapshot
Facile construction of 6-carbomethoxymethyl-3-methoxy-1,2-dioxane, a core structure of spongean anti-malarial peroxides
inferredcites →https://doi.org/10.1016/s0040-4039(01)80032-0openalex-snapshot
Peroxymercuration-demercuration of lipid hydroperoxides
inferredcites →https://doi.org/10.1016/s0040-4039(98)01248-9openalex-snapshot
A carbonyl oxide route to antimalarial yingzhaosu A analogues: Synthesis and antimalarial activity
inferredcites →https://doi.org/10.1016/s0960-894x(01)00673-4openalex-snapshot
New readily accessible peroxides with High Anti-malarial Potency
inferredcites →https://doi.org/10.1021/ar000080bopenalex-snapshot
How Might Qinghaosu (Artemisinin) and Related Compounds Kill the Intraerythrocytic Malaria Parasite? A Chemist's View
inferredcites →https://doi.org/10.1021/ja00317a059openalex-snapshot
Intramolecular alkoxypalladation/carbonylation of alkenes
inferredcites →https://doi.org/10.1021/ja00435a037openalex-snapshot
The formation of cyclic peroxides from unsaturated hydroperoxides: models for prostaglandin biosynthesis
inferredcites →https://doi.org/10.1021/ja00523a023openalex-snapshot
Palladium(II) tert-butyl peroxide carboxylates. New reagents for the selective oxidation of terminal olefins to methyl ketones. The role of peroxymetalation in selective oxidative processes
inferredcites →https://doi.org/10.1021/ja00545a036openalex-snapshot
Serial cyclization of peroxy free radicals: models for polyolefin oxidation
inferredcites →https://doi.org/10.1021/ja0394838openalex-snapshot
Stereoselective Synthesis of Tetrahydrofurans via the Palladium-Catalyzed Reaction of Aryl Bromides with γ-Hydroxy Alkenes: Evidence for an Unusual Intramolecular Olefin Insertion into a Pd(Ar)(OR) Intermediate
inferredcites →https://doi.org/10.1021/ja043203mopenalex-snapshot
Discovery of and Mechanistic Insight into a Ligand-Modulated Palladium-Catalyzed Wacker Oxidation of Styrenes Using TBHP
inferredcites →https://doi.org/10.1021/ja043278qopenalex-snapshot
Platinum-Catalyzed Intramolecular Hydroamination of Unactivated Olefins with Secondary Alkylamines
inferredcites →https://doi.org/10.1021/ja0460920openalex-snapshot
Palladium-Catalyzed Synthesis of N -Aryl-2-benzylindolines via Tandem Arylation of 2-Allylaniline: Control of Selectivity through in Situ Catalyst Modification
inferredcites →https://doi.org/10.1021/ja0477773openalex-snapshot
Platinum-Catalyzed Intramolecular Hydroalkoxylation of γ- and δ-Hydroxy Olefins to Form Cyclic Ethers
inferredcites →https://doi.org/10.1021/ja057489mopenalex-snapshot
Intramolecular Pd-Catalyzed Carboetherification and Carboamination. Influence of Catalyst Structure on Reaction Mechanism and Product Stereochemistry
inferredcites →https://doi.org/10.1021/ja060126hopenalex-snapshot
Room Temperature Palladium-Catalyzed Intramolecular Hydroamination of Unactivated Alkenes
inferredcites →https://doi.org/10.1021/ja0701614openalex-snapshot
Palladium-Catalyzed Methylation and Arylation of sp2 and sp3 C−H Bonds in Simple Carboxylic Acids
inferredcites →https://doi.org/10.1021/ja710126xopenalex-snapshot
Mild, Rhodium-Catalyzed Intramolecular Hydroamination of Unactivated Terminal and Internal Alkenes with Primary and Secondary Amines
inferredcites →https://doi.org/10.1021/jm020208qopenalex-snapshot
Antimalarial Activity of Yingzhaosu A Analogues
inferredcites →https://doi.org/10.1021/jo00006a028openalex-snapshot
Norsesterterpene peroxides from the sponge Latrunculia sp
inferredcites →https://doi.org/10.1021/jo00115a019openalex-snapshot
Enantioselective Total Syntheses and Stereochemical Studies of All Four Stereoisomers of Yingzhaosu C
inferredcites →https://doi.org/10.1021/jo00130a021openalex-snapshot
Diastereoselectivity of Additions to Chiral Carbonyl Oxides
inferredcites →https://doi.org/10.1021/jo00182a006openalex-snapshot
Stereochemistry of hydroperoxide cyclization reactions
inferredcites →https://doi.org/10.1021/jo00379a004openalex-snapshot
Trunculins A and B, norsesterterpene cyclic peroxides from a marine sponge, Latrunculia brevis
inferredcites →https://doi.org/10.1021/jo00444a055openalex-snapshot
Cyclic peroxides. 57. Prostanoid endoperoxide model compounds: 2,3-dioxabicyclo[2.2.1]heptane via selective diimide reduction
inferredcites →https://doi.org/10.1021/jo00912a037openalex-snapshot
Peroxy radical cyclization as a model for prostaglandin biosynthesis
inferredcites →https://doi.org/10.1021/jo01314a042openalex-snapshot
Palladium-catalyzed oxidation of terminal olefins to methyl ketones by hydrogen peroxide
inferredcites →https://doi.org/10.1021/jo0625958openalex-snapshot
Palladium-Catalyzed Highly Stereoselective Synthesis of N-Aryl-3-arylmethylisoxazolidines via Tandem Arylation of O-Homoallylhydroxylamines
inferredcites →https://doi.org/10.1021/jo991499mopenalex-snapshot
Halonium Ion-Mediated Reaction of Unsaturated Hydroperoxy Acetals. Competition between the Formation of Cyclic Peroxides and the Migration of the Methoxy (or Hydroxy) Group
inferredcites →https://doi.org/10.1021/np50096a007openalex-snapshot
Cytotoxicity of Artemisinin-Related Endoperoxides to Ehrlich Ascites Tumor Cells
inferredcites →https://doi.org/10.1021/np50112a006openalex-snapshot
New Cytotoxic Peroxylactones from the Marine Sponge, Plakinastrella onkodes
inferredcites →https://doi.org/10.1021/np800102uopenalex-snapshot
Diacarperoxides, Norterpene Cyclic Peroxides from the Sponge Diacarnus megaspinorhabdosa
inferredcites →https://doi.org/10.1021/ol0262340openalex-snapshot
Diverse Pathways for the Palladium(II)-Mediated Oxidation of Olefins by tert-Butylhydroperoxide
inferredcites →https://doi.org/10.1021/ol050291mopenalex-snapshot
Total Synthesis of Peroxyacarnoates A and D: Metal-Mediated Couplings as a Convergent Approach to Polyunsaturated Peroxides
inferredcites →https://doi.org/10.1021/ol051065fopenalex-snapshot
Intramolecular Additions of Alcohols and Carboxylic Acids to Inert Olefins Catalyzed by Silver(I) Triflate
inferredcites →https://doi.org/10.1039/b001780iopenalex-snapshot
Asymmetric epoxidation of electron-deficient olefins
inferredcites →https://doi.org/10.1039/b001854fopenalex-snapshot
Palladium(II)-catalyzed oxidation of terminal alkenes to methyl ketones using molecular oxygen
inferredcites →https://doi.org/10.1039/c39890000954openalex-snapshot
1,2-Dioxolane versus 1,2-dioxane formation in the cyclization of an α,ω-diene hydroperoxide under polar and free radical conditions
inferredcites →https://doi.org/10.1055/s-1995-5154openalex-snapshot
The Peroxide Changes Everything: New Methodology for the Synthesis of Peroxide-containing Natural Products
inferredcites →https://doi.org/10.1126/science.3887571openalex-snapshot
Qinghaosu (Artemisinin): an Antimalarial Drug from China
inferredcites →https://doi.org/10.1248/cpb.41.1324openalex-snapshot
Antifungal Peroxyketal Acids from an Okinawan Marine Sponge of Plakortis sp.
inferredcites →https://doi.org/10.2174/0929867013371608openalex-snapshot
Why Artemisinin and Certain Synthetic Peroxides are Potent Antimalarials. Implications for the Mode of Action
inferredcites →https://doi.org/10.2174/1385272013375346openalex-snapshot
Recent Advances in the Chemistry of Cyclic Peroxides
inferredcites →https://doi.org/10.2174/138955707780859396openalex-snapshot
Natural Peroxy Anticancer Agents
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.2022.113548zenodo-depositor-declared
Arteperoxides A–C, tris-normonoterpene–sesquiterpene conjugates with peroxide-bridges from Artemisia judaica exhibiting antiosteoclastogenic activity
inferred← citeshttps://doi.org/10.1002/9780471264194.fos11767openalex-snapshot
Palladium( II ) Acetate – Organic Oxidants
inferred← citeshttps://doi.org/10.1002/9781119972471.ch11openalex-snapshot
Addition Reactions: Polar Addition
inferred← citeshttps://doi.org/10.1002/adsc.201200110openalex-snapshot
Iron(III) Chloride‐Catalysed Aerobic Reduction of Olefins using Aqueous Hydrazine at Ambient Temperature
inferred← citeshttps://doi.org/10.1002/asia.201200166openalex-snapshot
Simple Analogues of Qinghaosu (Artemisinin)
inferred← citeshttps://doi.org/10.1002/chem.201003309openalex-snapshot
Total Synthesis of Plakortide E and Biomimetic Synthesis of Plakortone B
inferred← citeshttps://doi.org/10.1002/chem.201102716openalex-snapshot
Stereoselective Palladium‐Catalyzed Functionalization of Homoallylic Alcohols: A Convenient Synthesis of Di‐ and Trisubstituted Isoxazolidines and β‐Amino‐δ‐Hydroxy Esters
inferred← citeshttps://doi.org/10.1002/chem.201903752openalex-snapshot
Peroxycarbenium Ions as the “Gatekeepers” in Reaction Design: Assistance from Inverse Alpha‐Effect in Three‐Component β‐Alkoxy‐β‐peroxylactones Synthesis
inferred← citeshttps://doi.org/10.1002/chin.200305241openalex-snapshot
Six-Membered Ring Systems: With O and/or S Atoms
inferred← citeshttps://doi.org/10.1002/chin.200948161openalex-snapshot
ChemInform Abstract: Palladium(II)‐Catalyzed Cyclization of Unsaturated Hydroperoxides for the Synthesis of 1,2‐Dioxanes.
inferred← citeshttps://doi.org/10.1002/ejoc.201101477openalex-snapshot
Towards the Total Synthesis of Mycaperoxide B: Probing Biosynthetic Rationale
inferred← citeshttps://doi.org/10.1002/ejoc.201600038openalex-snapshot
CuI‐Catalyzed Synthesis of Propargyl Hydroperoxides Using Molecular Oxygen and Hydroxylamines
inferred← citeshttps://doi.org/10.1002/ejoc.70581openalex-snapshot
Enantiospecific Acid‐Catalysed Hydroperoxidation of Scalemic Tertiary Benzylic Alcohols Facilitating a Concise Asymmetric Synthesis of Yingzhaosu C
inferred← citeshttps://doi.org/10.1002/hlca.201200610openalex-snapshot
Electrochemical Phenylselenoetherification as a Key Step in the Synthesis of (±)‐Curcumene Ether
inferred← citeshttps://doi.org/10.1016/b978-0-08-096805-6.00015-2openalex-snapshot
Six-Membered Ring Systems
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00721-7openalex-snapshot
7.17 Addition Reactions with Formation of Carbon–Oxygen Bonds: (iv) The Wacker Oxidation and Related Reactions
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.80017-4openalex-snapshot
Addition Reactions with Formation of Carbon–Oxygen Bonds: (iv) The Wacker Oxidation and Related Reactions
inferred← citeshttps://doi.org/10.1016/bs.aihch.2021.03.001openalex-snapshot
Advances in the synthesis of 1,2-dioxolanes and 1,2-dioxanes
inferred← citeshttps://doi.org/10.1016/j.tet.2009.09.068openalex-snapshot
Asymmetric synthesis of 1,2-dioxanes: approaches to the peroxyplakoric acids
inferred← citeshttps://doi.org/10.1016/j.tet.2009.11.026openalex-snapshot
Synthesis of disubstituted 1,2-dioxolanes, 1,2-dioxanes, and 1,2-dioxepanes
inferred← citeshttps://doi.org/10.1016/j.tet.2018.03.040openalex-snapshot
Selective endoperoxide formation by heterogeneous TiO 2 photocatalysis with dioxygen
inferred← citeshttps://doi.org/10.1016/s0959-6380(11)22015-4openalex-snapshot
Six-Membered Ring Systems:
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c04629openalex-snapshot
Triethylamine-Catalyzed Cyclization of Unsaturated Hydroperoxides in the Presence of Triethylammonium Hydrochloride: A Synthesis of 1,2-Dioxanes
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Catalytic Enantioselective Peroxidation of α,β-Unsaturated Aldehydes for the Asymmetric Synthesis of Biologically Important Chiral Endoperoxides
inferred← citeshttps://doi.org/10.1021/jacs.6b11486openalex-snapshot
Palladium-Catalyzed Enantioselective Intermolecular Coupling of Phenols and Allylic Alcohols
inferred← citeshttps://doi.org/10.1021/jo1001559openalex-snapshot
Synthesis of Dihydroplakortin, 6-epi-Dihydroplakortin, and Their C10-Desethyl Analogues
inferred← citeshttps://doi.org/10.1021/ol101664yopenalex-snapshot
Palladium-Catalyzed Tandem Diperoxidation/C−H Activation Resulting in Diperoxy-oxindole in Air
inferred← citeshttps://doi.org/10.1021/ol300428qopenalex-snapshot
Endoperoxide Synthesis by Photocatalytic Aerobic [2 + 2 + 2] Cycloadditions
inferred← citeshttps://doi.org/10.1021/ol302848mopenalex-snapshot
Cu(II)-Catalyzed Aerobic Hydroperoxidation of Meldrum’s Acid Derivatives and Application in Intramolecular Oxidation: A Conceptual Blueprint for O2/H2Dihydroxylation
inferred← citeshttps://doi.org/10.1038/cddis.2013.68openalex-snapshot
Nox4-dependent ROS modulation by amino endoperoxides to induce apoptosis in cancer cells
inferred← citeshttps://doi.org/10.1039/c0cc02272aopenalex-snapshot
Organocatalytic diimide reduction of enamides in water
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An Yb(OTf) 3 and visible light relay catalyzed [3 + 2] cycloaddition/[3,3]-rearrangement/[4 + 2] cycloaddition in one pot to prepare oxazonine-fused endoperoxides
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Electrophysiological Responses of Bactrocera kraussi (Hardy) (Tephritidae) to Rectal Gland Secretions and Headspace Volatiles Emitted by Conspecific Males and Females
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Lewis Acids and Heteropoly Acids in the Synthesis of Organic Peroxides
inferred← citeshttps://doi.org/10.3762/bjoc.10.128openalex-snapshot
Cyclization–endoperoxidation cascade reactions of dienes mediated by a pyrylium photoredox catalyst
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Synthesis of five- and six-membered cyclic organic peroxides: Key transformations into peroxide ring-retaining products
inferred← citeshttps://doi.org/10.3762/bjoc.18.71openalex-snapshot
Structural basis for endoperoxide-forming oxygenases
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Nutrient concentration age dynamics of teak (Tectona grandis L.f.) plantations in Central America
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Développement de nouveaux composés leaders antimalariques de type endoperoxide à partir de sources naturelles ou synthétiques
inferred← citeshttps://doi.org/10.70675/892a61b4zb599z48c5z8ae8z29de20318e9fopenalex-snapshot
Synthetic studies toward plakortolides : asymmetric synthesis of ent-plakortolide I and seco-plakortolide E
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