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Organoseleno-Catalyzed Synthesis of α,β-Unsaturated α′-Alkoxy Ketones from Allenes Enabled by Se···O Interactions
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Carbonyl Activation by Selenium‐ and Tellurium‐Based Chalcogen Bonding in a Michael Addition Reaction
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The RuO4‐Catalyzed Ketohydroxylation, Part II:A Regio‐, Chemo‐ and Stereoselectivity Study
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Highly Selective Synthesis of [( Z )‐3‐Chloro‐2‐(phenylselanyl)‐1‐alkenyl]phosphonates and 2‐Ethoxy‐4‐(phenylselanyl)‐2,5‐dihydro‐1,2‐oxaphosphole 2‐Oxides by Electrophilic Reaction of 1,2‐Alkadienylphosphonates with PhSeCl
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Studies on electrophilic addition reaction of 2,3-allenoates with PhSeCl
inferredcites →https://doi.org/10.1016/j.tet.2009.04.023openalex-snapshot
Studies on highly regio- and stereoselective selenohydroxylation reaction of 1,2-allenyl phosphine oxides with PhSeCl
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Organoselenium-catalyzed enantioselective syn-dichlorination of unbiased alkenes
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The RuO4-Catalyzed Ketohydroxylation. Part 1. Development, Scope, and Limitation
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Electrophilic Interaction of 2,3-Allenoates with PhSeCl. An Unexpected Highly Stereoselective Synthesis of 3-Phenylseleno-4-oxo-2(E)-alkenoates
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Two-Directional Elaboration of Hydroxyacetone under Thermodynamically Controlled Conditions: Allylation or 2-Propynylation and Aldol Reaction
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inferredcites →https://doi.org/10.1039/c2cs35046gopenalex-snapshot
α-Hydroxy ketones as useful templates in asymmetric reactions
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inferredcites →https://doi.org/10.1055/s-0039-1690109openalex-snapshot
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inferredcites →https://doi.org/10.1351/pac200779020261openalex-snapshot
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Rational Design of Chiral Selenium-π-Acid Catalysts
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Electrophilic Selenium Catalysis with Electrophilic N-F Reagents as the Oxidants
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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A Theoretical Study on Organoselenium-Catalyzed Exo-Selective Oxidative Ring-Closing Reaction Promoted by 3 Different N-F Oxidants: Active Catalytic Species Screening, Reaction Mechanism, Origin of Exo-/Endo- and (E)-/(Z)- Selectivities, and the Influence of Different Reagents on Reaction Yields
inferred← citeshttps://doi.org/10.1007/s11144-025-02949-2openalex-snapshot
A theoretical study of organoselenium-catalyzed oxidative ring-closing reaction: structure/selectivity/yield relationships
inferred← citeshttps://doi.org/10.1016/j.mcat.2024.114442openalex-snapshot
Both N-F oxidant and NaF determined reaction yield in the organoselenium-catalyzed oxidative ring-closing reaction of unsaturated alcohol: A theoretical study
inferred← citeshttps://doi.org/10.1021/acs.chemrev.0c00986openalex-snapshot
Deciphering the Chameleonic Chemistry of Allenols: Breaking the Taboo of a Onetime Esoteric Functionality
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00167openalex-snapshot
Meyer–Schuster-Type Rearrangement of Propargylic Alcohols into α-Selenoenals and -enones with Diselenides
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02681openalex-snapshot
The Synthesis of α-Keto Acetals from Terminal Alkynes and Alcohols via Synergistic Interaction of Organoselenium Catalysis and Electrochemical Oxidation
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c01983openalex-snapshot
Electrochemical Organoselenium-Catalyzed Intermolecular Hydroazolylation of Alkenes with Low Catalyst Loadings
inferred← citeshttps://doi.org/10.1021/acscatal.4c01327openalex-snapshot
Intermolecular Aza-Wacker Coupling of Alkenes with Azoles by Photo-Aerobic Selenium-π-Acid Multicatalysis
inferred← citeshttps://doi.org/10.1039/d2cc01901aopenalex-snapshot
Electrochemical selenium–π–acid promoted hydration of alkynyl phosphonates
inferred← citeshttps://doi.org/10.1039/d3ob01116jopenalex-snapshot
Electrochemical selenium-catalyzed para -amination of N -aryloxyamides: access to polysubstituted aminophenols
inferred← citeshttps://doi.org/10.1055/a-2169-3807openalex-snapshot
Recent Advances in Electrochemically Mediated Reactions of Diselenides
inferred← citeshttps://doi.org/10.1246/cl.210065openalex-snapshot
Selenium-catalyzed Functionalization of Alkynes
inferred← citeshttps://doi.org/10.2139/ssrn.4968864openalex-snapshot
How Did Hypervalent Iodide Oxidant Species Influence Reaction Yield of Organoselenium-Catalzyed Oxidative Ring-Closing Reaction of (E)-4-Phenylbut-3-Enoic Acid? A Theoretical Study
inferred← citeshttps://doi.org/10.3390/molecules28186614openalex-snapshot
Recent Advances in the Use of Diorganyl Diselenides as Versatile Catalysts
inferred← citeshttps://doi.org/10.6023/cjoc202508009openalex-snapshot
Research Progress in Electrophilic Selenium-Catalyzed Rearrangement Reactions
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