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Total Synthesis of Asperchalasines A, D, E, and H
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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/(sici)1521-3765(20000417)6:8<1302::aid-chem1302>3.0.co;2-jopenalex-snapshot
Diastereo- and Enantioselective Total Synthesis of Stigmatellin A
inferredcites →https://doi.org/10.1002/ange.201407088openalex-snapshot
Biomimetic Synthesis of the Calcineurin Phosphatase Inhibitor Dibefurin
inferredcites →https://doi.org/10.1002/ange.201506264openalex-snapshot
Asperchalasine A, a Cytochalasan Dimer with an Unprecedented Decacyclic Ring System, from Aspergillus flavipes
inferredcites →https://doi.org/10.1002/ange.201511315openalex-snapshot
Epicochalasines A and B: Two Bioactive Merocytochalasans Bearing Caged Epicoccine Dimer Units from Aspergillus flavipes
inferredcites →https://doi.org/10.1002/ange.201602439openalex-snapshot
Total Syntheses of Periconiasins A–E
inferredcites →https://doi.org/10.1002/ange.201701125openalex-snapshot
Asperflavipine A: A Cytochalasan Heterotetramer Uniquely Defined by a Highly Complex Tetradecacyclic Ring System from Aspergillus flavipes QCS12
inferredcites →https://doi.org/10.1002/anie.201407088openalex-snapshot
Biomimetic Synthesis of the Calcineurin Phosphatase Inhibitor Dibefurin
inferredcites →https://doi.org/10.1002/anie.201506264openalex-snapshot
Asperchalasine A, a Cytochalasan Dimer with an Unprecedented Decacyclic Ring System, from Aspergillus flavipes
inferredcites →https://doi.org/10.1002/anie.201511315openalex-snapshot
Epicochalasines A and B: Two Bioactive Merocytochalasans Bearing Caged Epicoccine Dimer Units from Aspergillus flavipes
inferredcites →https://doi.org/10.1002/anie.201602439openalex-snapshot
Total Syntheses of Periconiasins A–E
inferredcites →https://doi.org/10.1002/anie.201701125openalex-snapshot
Asperflavipine A: A Cytochalasan Heterotetramer Uniquely Defined by a Highly Complex Tetradecacyclic Ring System from Aspergillus flavipes QCS12
inferredcites →https://doi.org/10.1002/chem.201603734openalex-snapshot
First Total Synthesis, Structure Revision, and Natural History of the Smallest Cytochalasin: (+)‐Periconiasin G
inferredcites →https://doi.org/10.1002/hlca.19930760710openalex-snapshot
Approaches to the Synthesis of Cytochalasans. Part 11. Further transformations and cyclization attempts directed towards proxiphomin
inferredcites →https://doi.org/10.1016/j.imbio.2012.05.015openalex-snapshot
Chaetoglobosin F, a small molecule compound, possesses immunomodulatory properties on bone marrow-derived dendritic cells via TLR9 signaling pathway
inferredcites →https://doi.org/10.1016/j.tet.2011.09.079openalex-snapshot
Identification of an unexpected 2-oxonia[3,3]sigmatropic rearrangement/aldol pathway in the formation of oxacyclic rings. Total synthesis of (+)-aspergillin PZ
inferredcites →https://doi.org/10.1016/j.tetlet.2006.05.176openalex-snapshot
Mild and efficient deprotection of allyl ethers of phenols and hydroxycoumarins using a palladium on charcoal catalyst and ammonium formate
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Indium- and Zinc-Mediated Acyloxyallylation of Protected and Unprotected Aldotetroses─Revealing a Pronounced Diastereodivergence and a Fundamental Difference in the Performance of the Mediating Metal
inferredcites →https://doi.org/10.1021/acs.orglett.7b02146openalex-snapshot
Aspergilasines A–D: Four Merocytochalasans with New Carbon Skeletons from Aspergillus flavipes QCS12
inferredcites →https://doi.org/10.1021/ja00203a042openalex-snapshot
Palladium-catalyzed synthesis of macrocycles. A total synthesis of (-)-aspochalasin B
inferredcites →https://doi.org/10.1021/ja00222a047openalex-snapshot
A sulfur-mediated total synthesis of Zygosporin E
inferredcites →https://doi.org/10.1021/ja00354a072openalex-snapshot
A simplified total synthesis of cytochalasins via an intramolecular Diels-Alder reaction
inferredcites →https://doi.org/10.1021/ja00492a082openalex-snapshot
Total synthesis of cytochalasin B
inferredcites →https://doi.org/10.1021/ja503972popenalex-snapshot
Total Synthesis of Taiwaniadducts B, C, and D
inferredcites →https://doi.org/10.1021/jf304314gopenalex-snapshot
Nematicidal Activity of Chaetoglobosin A Poduced by Chaetomium globosum NK102 against Meloidogyne incognita
inferredcites →https://doi.org/10.1021/jo00021a027openalex-snapshot
Organic oxoammonium salts. 3. A new convenient method for the oxidation of alcohols to aldehydes and ketones
inferredcites →https://doi.org/10.1021/jo00215a004openalex-snapshot
The Horner-Wadsworth-Emmons modification of the Wittig reaction using triethylamine and lithium or magnesium salts
inferredcites →https://doi.org/10.1021/jo00347a034openalex-snapshot
Synthesis of the cytochalasin D isoindolone unit: solutions to the problem of regiochemistry in N-benzoylpyrrolinone Diels-Alder reactions
inferredcites →https://doi.org/10.1021/jo00370a004openalex-snapshot
The preparation and reactions of naphtho[1,2-c]furan and naphtho[2,3-c]furan
inferredcites →https://doi.org/10.1021/jo00370a019openalex-snapshot
Stereochemistry of lithium dialkylamide-induced 1,4-eliminations leading to substituted isobenzofurans
inferredcites →https://doi.org/10.1021/jo00910a044openalex-snapshot
Synthesis of the isoindolone nucleus of the cytochalasins
inferredcites →https://doi.org/10.1021/jo0100188openalex-snapshot
Synthesis of Oxa-Bridged Analogues of Farnesyltransferase Inhibitor RPR 115135
inferredcites →https://doi.org/10.1021/ol101760mopenalex-snapshot
Dual Fluorescent N-Aryl-2,3- naphthalimides: Applications in Ratiometric DNA Detection and White Organic Light-Emitting Devices
inferredcites →https://doi.org/10.1021/ol400458nopenalex-snapshot
Periconiasins A–C, New Cytotoxic Cytochalasans with an Unprecedented 9/6/5 Tricyclic Ring System from Endophytic Fungus Periconia sp.
inferredcites →https://doi.org/10.1021/ol401186fopenalex-snapshot
Synthesis of Eukaryotic Translation Elongation Inhibitor Lactimidomycin via Zn(II)-Mediated Horner–Wadsworth–Emmons Macrocyclization
inferredcites →https://doi.org/10.1038/leu.2013.360openalex-snapshot
Chaetoglobosin A preferentially induces apoptosis in chronic lymphocytic leukemia cells by targeting the cytoskeleton
inferredcites →https://doi.org/10.1038/nchem.2336openalex-snapshot
An eight-step synthesis of epicolactone reveals its biosynthetic origin
inferredcites →https://doi.org/10.1039/a906412eopenalex-snapshot
Total synthesis of cytochalasin D: total synthesis and full structural assignment of cytochalasin O
inferredcites →https://doi.org/10.1039/b903913aopenalex-snapshot
The chemistry and biology of cytochalasans
inferredcites →https://doi.org/10.1039/c39860000727openalex-snapshot
Cytochalasan synthesis: total synthesis of cytochalasin H
inferredcites →https://doi.org/10.1039/c39860001447openalex-snapshot
Cytochalasan synthesis: total synthesis of cytochalasin G
inferredcites →https://doi.org/10.1039/c39900000464openalex-snapshot
Cytochalasan synthesis: total synthesis of cytochalasin D
inferredcites →https://doi.org/10.1039/c4ob01308eopenalex-snapshot
Approaches to the total synthesis of chaetochalasin A
inferredcites →https://doi.org/10.1039/p19890000499openalex-snapshot
Cytochalasan synthesis: total synthesis of the naturally occurring [13]cytochalasan proxiphomin
inferredcites →https://doi.org/10.1055/s-0030-1259031openalex-snapshot
Regioselective Alkylation of Catechols via Mitsunobu Reactions
inferredcites →https://doi.org/10.1073/pnas.0402111101openalex-snapshot
An enantioselective, modular, and general route to the cytochalasins: Synthesis of L-696,474 and cytochalasin B
inferredcites →https://doi.org/10.1080/00397918608056378openalex-snapshot
An Intramolecular Diels-alder Reaction of a Z-Diene. Generation Of The Chiral Isoindolone Nucleus Of Cytochalasin C.1
inferredcites →https://doi.org/10.1248/cpb.54.1662openalex-snapshot
Biomimetic Synthesis of (.+-.)-Galanthamine and Asymmetric Synthesis of (-)-Galanthamine Using Remote Asymmetric Induction
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Olefination, Metathesis, and Epoxidation Reactions
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Multifaceted Domino Knoevenagel‐Cyclization Reactions; Four Movements for 2H‐Chromenes and Chromans
inferred← citeshttps://doi.org/10.1002/ange.201809703openalex-snapshot
Biomimetic Synthesis of (+)‐Aspergillin PZ
inferred← citeshttps://doi.org/10.1002/ange.201911978openalex-snapshot
Total Synthesis of (−)‐Perezoperezone through an Intermolecular [5+2] Homodimerization of Hydroxy p‐Quinone
inferred← citeshttps://doi.org/10.1002/ange.202102831openalex-snapshot
Bioinspired Network Analysis Enabled Divergent Syntheses and Structure Revision of Pentacyclic Cytochalasans
inferred← citeshttps://doi.org/10.1002/ange.202422615openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.202502766openalex-snapshot
Cooperative Redox Reactions Encoded by Two Gene Clusters Enable Intermolecular Cycloaddition Cascade for the Formation of Meroaspochalasins
inferred← citeshttps://doi.org/10.1002/anie.201809703openalex-snapshot
Biomimetic Synthesis of (+)‐Aspergillin PZ
inferred← citeshttps://doi.org/10.1002/anie.201911978openalex-snapshot
Total Synthesis of (−)‐Perezoperezone through an Intermolecular [5+2] Homodimerization of Hydroxy p‐Quinone
inferred← citeshttps://doi.org/10.1002/anie.202102831openalex-snapshot
Bioinspired Network Analysis Enabled Divergent Syntheses and Structure Revision of Pentacyclic Cytochalasans
inferred← citeshttps://doi.org/10.1002/anie.202422615openalex-snapshot
Total Synthesis of Lugdunomycin via Sequential Photoinduced Spiroketalization and Isobenzofuran Diels–Alder Reactions
inferred← citeshttps://doi.org/10.1002/anie.202502766openalex-snapshot
Cooperative Redox Reactions Encoded by Two Gene Clusters Enable Intermolecular Cycloaddition Cascade for the Formation of Meroaspochalasins
inferred← citeshttps://doi.org/10.1002/anie.202524740openalex-snapshot
Bioinspired Total Synthesis of Curtachalasin B and Biosynthetically Related Cytochalasans
inferred← citeshttps://doi.org/10.1002/cjoc.202200215openalex-snapshot
Ergochaeglobosins A—E, Unprecedented Heterodimers of Cytochalasan and Ergosterol fromChaeglobosin globosum P2 ‐2‐2
inferred← citeshttps://doi.org/10.1007/978-3-030-59444-2_1openalex-snapshot
Progress in the Chemistry of Cytochalasans
inferred← citeshttps://doi.org/10.1007/978-3-030-92030-2_1openalex-snapshot
Complex Natural Products Derived from Pyrogallols
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Michael Acceptor Pyrrolidone Derivatives and Their Activity against Diffuse Large B-cell Lymphoma
inferred← citeshttps://doi.org/10.1007/s13659-025-00572-1openalex-snapshot
Harziachalasins A–G, polycyclic-fused cytochalasins from the endophytic fungus Trichoderma harzianum MLJ-4 with HIV latency reversal activity
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00056-9openalex-snapshot
[5 + 2] and [6 + 2] Cycloaddition Reaction of Alkenes, Alkynes, Allenes and 1,3-Dienes
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00082-xopenalex-snapshot
Wittig and Horner-Wadsworth-Emmons Reactions
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inferred← citeshttps://doi.org/10.1016/j.chempr.2020.11.010openalex-snapshot
Biosynthetically Inspired Divergent Syntheses of Merocytochalasans
inferred← citeshttps://doi.org/10.1016/j.eng.2024.12.013openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tchem.2022.100022openalex-snapshot
Collective total syntheses of cytochalasans and merocytochalasans
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Phosphamide-Mediated C═N Condensation through the Horner–Wadsworth–Emmons-Type Reaction: A Sustainable Route for Polyphosphamide Upcycling
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Cysteine Residue Containing Merocytochalasans and 17,18-seco-Aspochalasins from Aspergillus micronesiensis
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Flavipesines A and B and Asperchalasines E–H: Cytochalasans and Merocytochalasans from Aspergillus flavipes
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Bisaspochalasins D and E: Two Heterocycle-Fused Cytochalasan Homodimers from an Endophytic Aspergillus flavipes
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Dimericchalasine A and Amichalasines D and E: Unexpected Cytochalasan Homodimer and Heterotrimers from Aspergillus micronesiensis PG-1
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Bisaspochalasins A–C: Three Cytochalasan Homodimers with Highly Fused Ring System from an Endophytic Aspergillus flavipes
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Cytochathiazines A–C: Three Merocytochalasans with a 2 H -1,4-Thiazine Functionality from Coculture of Chaetomium globosum and Aspergillus flavipes
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Berberine bridge enzyme-like oxidase-catalysed double bond isomerization acts as the pathway switch in cytochalasin synthesis
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