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Tandem Oxidative Cyclization with Rhenium Oxide. Total Synthesis of 17,18-bisepi-Goniocin
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Goniocin from Goniothalamus giganteus: The first tri-THF annonaceous acetogenin
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Stereocontrolled oxidation of 5-hydroxyalkenes with rhenium oxide. III
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Oxidative cyclization of 5-hydroxyalkenes with rhenium oxide, utilizing a co-oxidant. IV
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Recent Advances in Phytochemistry
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Catalytic Asymmetric Dihydroxylation
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Multiple bonds between transition metals and main-group elements. 124. Structures and reactivity of acylperrhenates
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Total synthesis of naturally occurring acetogenins: solamin and reticulatacin
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Combined Osmium-Rhenium Approach to Synthesis of Naturally Occurring Polyethers
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A general approach to enantiomerically pure methylcarbinols. Asymmetric synthesis of antibiotic (-)-A26771B and the WCR sex pheromone
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Acylperrhenate-Induced Tandem syn-Oxidative Cyclizations of Hydroxydienes
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Toward Chemical Libraries of Annonaceous Acetogenins. Total Synthesis of Trilobacin
inferredcites →https://doi.org/10.1021/jo9614811openalex-snapshot
Total Synthesis of (+)-Aspicilin. The Naked Carbon Skeleton Strategy vs the Bioorganic Approach
inferredcites →https://doi.org/10.1039/dt9840002695openalex-snapshot
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inferredcites →https://doi.org/10.1039/np9961300275openalex-snapshot
Recent advances in annonaceous acetogenins
inferredcites →https://doi.org/10.1351/pac199769030423openalex-snapshot
Towards chemical libraries of annonaceous acetogenins
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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A Facile Route to Bulladecin-Type Acetogenins - Total Synthesis of Asimilobinand Correction of the Configuration of Its Tetrahydrofuran Segment
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Fehlschläge und Umwege bei Totalsynthesen in den neunziger Jahren
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ChemInform Abstract: Tandem Oxidative Cyclization with Rhenium Oxide. Total Synthesis of 17,18‐bisepi‐Goniocin.
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inferred← citeshttps://doi.org/10.1016/j.tet.2003.10.095openalex-snapshot
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