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Cascade Vinyl Radical Ipso-Cyclization Reactions and the Formation of α,β-Unsaturated-β-aryl-γ-lactams from N-Propargyl Benzamides | The Journal of Organic Chemistry
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Wet carbonate-promoted radical arylation of vinyl pinacolboronates with diaryliodonium salts yields substituted olefins | Communications Chemistry
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PDF] Radical Enamination of Vinyl Azides: Direct Synthesis of N-Unprotected Enamines. | Semantic Scholar
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Photoredox-Mediated Deoxygenative Radical Additions of Aromatic Acids to Vinyl Boronic Esters and gem-Diborylalkenes | Organic Chemistry | ChemRxiv | Cambridge Open Engage
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Photochemical Generation and Structure of Vinyl Radicals - Goumans - 2008 - European Journal of Organic Chemistry - Wiley Online Library
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Cascade Vinyl Radical Ipso-Cyclization Reactions and the Formation of α,β-Unsaturated-β-aryl-γ-lactams from N-Propargyl Benzamides | The Journal of Organic Chemistry
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Direct Radical Polymerization of Vinyl Ethers: Reversible Addition–Fragmentation Chain Transfer Polymerization of Hydroxy-Functional Vinyl Ethers | Macromolecules
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The mechanism of free-radical polymerization of vinyl chloride monomer... | Download Scientific Diagram
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Hydrogen radical-shuttle (HRS)-enabled photoredox synthesis of indanones via decarboxylative annulation | Nature Communications
![PDF] Radical Enamination of Vinyl Azides: Direct Synthesis of N-Unprotected Enamines. | Semantic Scholar PDF] Radical Enamination of Vinyl Azides: Direct Synthesis of N-Unprotected Enamines. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/ad4e62b83576af821a221a0a20bd8ad9ee8a9ff9/2-Table1-1.png)
PDF] Radical Enamination of Vinyl Azides: Direct Synthesis of N-Unprotected Enamines. | Semantic Scholar
![What's the chemical explanation for why vinyl radicals and carbocations are so unstable? Does it have something to do with p orbitals? I'm honestly not really sure, but am very curious. Thanks! : What's the chemical explanation for why vinyl radicals and carbocations are so unstable? Does it have something to do with p orbitals? I'm honestly not really sure, but am very curious. Thanks! :](https://i.redd.it/ijd2tlt6fd061.jpg)
What's the chemical explanation for why vinyl radicals and carbocations are so unstable? Does it have something to do with p orbitals? I'm honestly not really sure, but am very curious. Thanks! :
Radical 1,2,3-tricarbofunctionalization of α-vinyl-β-ketoesters enabled by a carbon shift from an all-carbon quaternary center - Chemical Science (RSC Publishing)
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