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K 2 S 2 O 8 /TEMPO-Induced Cascade Oxidative Cyclization/1,2-Migration of Electron-Deficient Groups: Strategy for the Construction of 1 H -Pyrrol-2(3 H )-ones

https://doi.org/10.1021/acs.orglett.8b01402

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Combination of Cp*RhIII‐Catalyzed C−H Activation and a Wagner–Meerwein‐Type Rearrangement

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Metal‐Free Oxidative Radical Addition of Carbonyl Compounds to α,α‐Diaryl Allylic Alcohols: Synthesis of Highly Functionalized Ketones

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Palladium-catalyzed oxidative cyclopropanation of enamides and norbornenes initiated by C–H activation

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Synthesis, cytotoxic activity, and tubulin polymerization inhibitory activity of new pyrrol-2(3H)-ones and pyridazin-3(2H)-ones

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Base-mediated formal [3+2] cycloaddition of β,γ-alkenyl esters and p-TsN3 for the synthesis of pyrazoles

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1,2-Acyl group migration in the oxidative free radical reaction of 2-substituted-1,4-quinones

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Acid promoted dimerization of β-amino-α,β-unsaturated amides affording bis(functionalized) pyrrolinones

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Carbon–Carbon Bond Forming Reactions via Photogenerated Intermediates

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In Situ Generated TEMPO Oxoammonium Salt Mediated Tandem Cyclization of β-Oxoamides with Amine Hydrochlorides for the Synthesis of Pyrrolin-4-ones

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Visible-Light Induced and Oxygen-Promoted Oxidative Cyclization of Aromatic Enamines for the Synthesis of Quinolines Derivatives

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TBHP/TBAI-Mediated Oxidative Cascade Reaction Consisting of Dimerization, Cyclization, and 1,2-Aryl Migration: Metal-Free Synthesis of Pyrrolin-4-ones and Highly Substituted Pyrroles

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Metal/Benzoyl Peroxide (BPO)-Controlled Chemoselective Cycloisomerization of (o-Alkynyl)phenyl Enaminones: Synthesis of α-Naphthylamines and Indeno[1,2-c]pyrrolones

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Iron-Promoted Difunctionalization of Alkenes by Phenylselenylation/1,2-Aryl Migration

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Highly Efficient Iridium-Catalyzed Asymmetric Hydrogenation of Unprotected β-Enamine Esters

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Mechanism of the Oxidation of Alcohols by Oxoammonium Cations

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Switching between Concerted and Stepwise Mechanisms for Dyotropic Rearrangements of β-Lactones Leading to Spirocyclic, Bridged γ-Butyrolactones

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Oxidative Rearrangement of Tertiary Allylic Alcohols Employing Oxoammonium Salts

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

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