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Synthesis and Antiplasmodial Activity of Bicyclic Dioxanes as Simplified Dihydroplakortin Analogues

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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/cmdc.200700108openalex-snapshot
The Fe 2+ ‐Mediated Decomposition, PfATP6 Binding, and Antimalarial Activities of Artemisone and Other Artemisinins: The Unlikelihood of C‐Centered Radicals as Bioactive Intermediates
inferredcites →https://doi.org/10.1002/cmdc.201000508openalex-snapshot
Reactions of Antimalarial Peroxides with Each of Leucomethylene Blue and Dihydroflavins: Flavin Reductase and the Cofactor Model Exemplified
inferredcites →https://doi.org/10.1016/j.cbpa.2007.05.038openalex-snapshot
Drug discovery for malaria: a very challenging and timely endeavor
inferredcites →https://doi.org/10.1016/j.tetlet.2003.09.033openalex-snapshot
Co(thd)2: a superior catalyst for aerobic epoxidation and hydroperoxysilylation of unactivated alkenes: application to the synthesis of spiro-1,2,4-trioxanes
inferredcites →https://doi.org/10.1016/j.tetlet.2009.07.137openalex-snapshot
Synthetic studies toward 1,2-dioxanes as precursors of potential endoperoxide-containing antimalarials
inferredcites →https://doi.org/10.1016/j.tips.2008.07.004openalex-snapshot
Artemisinins: their growing importance in medicine
inferredcites →https://doi.org/10.1016/s0040-4020(99)00332-4openalex-snapshot
Metabolites from the sponge Plakortis simplex. Determination of absolute stereochemistry of plakortin. Isolation and stereostructure of three plakortin related compounds
inferredcites →https://doi.org/10.1016/s0140-6736(10)61963-0openalex-snapshot
Artemisinin resistance—the clock is ticking
inferredcites →https://doi.org/10.1021/jm060899gopenalex-snapshot
Endoperoxide Derivatives from Marine Organisms: 1,2-Dioxanes of the Plakortin Family as Novel Antimalarial Agents
inferredcites →https://doi.org/10.1021/jo1001559openalex-snapshot
Synthesis of Dihydroplakortin, 6-epi-Dihydroplakortin, and Their C10-Desethyl Analogues
inferredcites →https://doi.org/10.1039/a902202copenalex-snapshot
The influence of natural products upon drug discovery (Antiquity to late 1999)
inferredcites →https://doi.org/10.1039/b918600jopenalex-snapshot
Insight into the mechanism of action of plakortins, simple 1,2-dioxaneantimalarials
inferredcites →https://doi.org/10.1056/nejmoa0808859openalex-snapshot
Artemisinin Resistance in Plasmodium falciparum Malaria
inferredcites →https://doi.org/10.1093/jac/dkg008openalex-snapshot
Activity against Plasmodium falciparum of cycloperoxide compounds obtained from the sponge Plakortis simplex
inferredcites →https://doi.org/10.1126/science.1155165openalex-snapshot
Qinghaosu (Artemisinin): The Price of Success
inferredcites →https://doi.org/10.1186/1475-2875-10-s1-s2openalex-snapshot
How can natural products serve as a viable source of lead compounds for the development of new/novel anti-malarials?
inferredcites →https://doi.org/10.1371/journal.pone.0009582openalex-snapshot
Artemisinin Directly Targets Malarial Mitochondria through Its Specific Mitochondrial Activation

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Arteperoxides A–C, tris-normonoterpene–sesquiterpene conjugates with peroxide-bridges from Artemisia judaica exhibiting antiosteoclastogenic activity
inferred← citeshttps://doi.org/10.1002/ejoc.201101852openalex-snapshot
Controlled Reactions of 2,3‐Allenoates with a 1,3‐Diketone Catalyst Effect
inferred← citeshttps://doi.org/10.1002/ejoc.201402895openalex-snapshot
Six Peroxide Groups in One Molecule – Synthesis of Nine‐Membered Bicyclic Silyl Peroxides
inferred← citeshttps://doi.org/10.1007/s00706-014-1349-8openalex-snapshot
Synthesis of new carbacyclic analogs of trolox
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.bioorg.2019.103020openalex-snapshot
Bridged bicyclic 2,3-dioxabicyclo[3.3.1]nonanes as antiplasmodial agents: Synthesis, structure-activity relationships and studies on their biomimetic reaction with Fe(II)
inferred← citeshttps://doi.org/10.1016/j.bmcl.2015.09.007openalex-snapshot
Exploring clotrimazole-based pharmacophore: 3D-QSAR studies and synthesis of novel antiplasmodial agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2018.11.004openalex-snapshot
Structure-activity relationships, biological evaluation and structural studies of novel pyrrolonaphthoxazepines as antitumor agents
inferred← citeshttps://doi.org/10.1016/j.jff.2020.104231openalex-snapshot
Enhancement of nutritional soy protein and peptide supplementation on skin repair in rats
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.12.075openalex-snapshot
A synthetic strategy to bridged 2,3,8-trioxabicyclo[3,3,1]nonane endoperoxides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.10.059openalex-snapshot
Synthetic studies toward bicyclic endoperoxides presenting polar side chains
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.02.042openalex-snapshot
Kharasch reaction: Cu-catalyzed and non-Kharasch metal-free peroxidation of barbituric acids
inferred← citeshttps://doi.org/10.1021/acs.joc.5b01326openalex-snapshot
An SN1-type Reaction To Form the 1,2-Dioxepane Ring: Synthesis of 10,12-Peroxycalamenene
inferred← citeshttps://doi.org/10.1021/acs.organomet.6b00129openalex-snapshot
Reduction of Organosilicon Peroxides: Ring Contraction and Cyclodimerization
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c00295openalex-snapshot
Organocatalytic Enantioselective γ-Elimination: Applications in the Preparation of Chiral Peroxides and Epoxides
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c00056openalex-snapshot
Sc(OTf)3-Catalyzed C–C Bond-Forming Reaction of Cyclic Peroxy Ketals for the Synthesis of Highly Functionalized 1,2-Dioxene Endoperoxides
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c01607openalex-snapshot
Stereoselective Oxidative Cyclization of N -Allyl Benzamides to Oxaz(ol)ines
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
inferred← citeshttps://doi.org/10.1021/acscatal.7b02754openalex-snapshot
Copper-Catalyzed Silylperoxidation Reaction of α,β-Unsaturated Ketones, Esters, Amides, and Conjugated Enynes
inferred← citeshttps://doi.org/10.1021/jm300802sopenalex-snapshot
Optimization of 4-Aminoquinoline/Clotrimazole-Based Hybrid Antimalarials: Further Structure–Activity Relationships, in Vivo Studies, and Preliminary Toxicity Profiling
inferred← citeshttps://doi.org/10.1021/jm300831bopenalex-snapshot
Mimicking the Intramolecular Hydrogen Bond: Synthesis, Biological Evaluation, and Molecular Modeling of Benzoxazines and Quinazolines as Potential Antimalarial Agents
inferred← citeshttps://doi.org/10.1021/om500095xopenalex-snapshot
Nature Chooses Rings: Synthesis of Silicon-Containing Macrocyclic Peroxides
inferred← citeshttps://doi.org/10.1039/c4md00454jopenalex-snapshot
Synthetic spirocyclic endoperoxides: new antimalarial scaffolds
inferred← citeshttps://doi.org/10.1039/c5np00142kopenalex-snapshot
Structural diversity and chemical synthesis of peroxide and peroxide-derived polyketide metabolites from marine sponges
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Advances in the synthesis of acyclic peroxides
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One-Carbon Homologation of Pyrrole Carboxaldehyde via Wittig Reaction and Mild Hydrolysis of Vinyl Ether – toward the Synthesis of a Sterically Locked Phytochrome Chromophore
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