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![Metal-Catalyzed Oxa-[4+2] Cyclizations of Quinone Methides with Alkynyl Benzyl Alcohols | The Journal of Organic Chemistry](https://pubs.acs.org/cms/10.1021/acs.joc.8b02186/asset/images/medium/jo-2018-021867_0002.gif "Metal-Catalyzed Oxa-[4+2] Cyclizations of Quinone Methides with Alkynyl Benzyl Alcohols | The Journal of Organic Chemistry")
Metal-Catalyzed Oxa-[4+2] Cyclizations of Quinone Methides with Alkynyl Benzyl Alcohols | The Journal of Organic Chemistry
![Organophotoredox-Catalyzed Intermolecular Oxa-[4+2] Cycloaddition Reactions | The Journal of Organic Chemistry](https://pubs.acs.org/cms/10.1021/acs.joc.9b01156/asset/images/large/jo9b01156_0006.jpeg "Organophotoredox-Catalyzed Intermolecular Oxa-[4+2] Cycloaddition Reactions | The Journal of Organic Chemistry")
Organophotoredox-Catalyzed Intermolecular Oxa-[4+2] Cycloaddition Reactions | The Journal of Organic Chemistry
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Nitrated Confined Imidodiphosphates Enable a Catalytic Asymmetric Oxa-Pictet–Spengler Reaction | Journal of the American Chemical Society
Synthesis of α,α′-trans-Oxepanes through an Organocatalytic Oxa-conjugate Addition Reaction | Organic Letters
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Asymmetric Synthesis of Cyclohexenone-Fused Isochromans via Quinidine-Catalyzed Domino Peroxyhemiacetalization/Oxa-Michael Addition/Desymmetrization Sequence | The Journal of Organic Chemistry
![Intramolecular Hydrogen Abstraction Reaction Promoted by N-Radicals in Carbohydrates. Synthesis of Chiral 7-Oxa-2-azabicyclo[2.2.1]heptane and 8- Oxa-6-azabicyclo[3.2.1]octane Ring Systems | The Journal of Organic Chemistry](https://pubs.acs.org/cms/10.1021/jo026314h/asset/images/medium/jo026314hh00003.gif "Intramolecular Hydrogen Abstraction Reaction Promoted by N-Radicals in Carbohydrates. Synthesis of Chiral 7-Oxa-2-azabicyclo[2.2.1]heptane and 8- Oxa-6-azabicyclo[3.2.1]octane Ring Systems | The Journal of Organic Chemistry")
Intramolecular Hydrogen Abstraction Reaction Promoted by N-Radicals in Carbohydrates. Synthesis of Chiral 7-Oxa-2-azabicyclo[2.2.1]heptane and 8- Oxa-6-azabicyclo[3.2.1]octane Ring Systems | The Journal of Organic Chemistry
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![Intramolecular Hydrogen Abstraction Reaction Promoted by N-Radicals in Carbohydrates. Synthesis of Chiral 7-Oxa-2-azabicyclo[2.2.1]heptane and 8- Oxa-6-azabicyclo[3.2.1]octane Ring Systems | The Journal of Organic Chemistry](https://pubs.acs.org/cms/10.1021/jo026314h/asset/images/medium/jo026314hh00002.gif "Intramolecular Hydrogen Abstraction Reaction Promoted by N-Radicals in Carbohydrates. Synthesis of Chiral 7-Oxa-2-azabicyclo[2.2.1]heptane and 8- Oxa-6-azabicyclo[3.2.1]octane Ring Systems | The Journal of Organic Chemistry")
Intramolecular Hydrogen Abstraction Reaction Promoted by N-Radicals in Carbohydrates. Synthesis of Chiral 7-Oxa-2-azabicyclo[2.2.1]heptane and 8- Oxa-6-azabicyclo[3.2.1]octane Ring Systems | The Journal of Organic Chemistry
Synthesis of α,α′-trans-Oxepanes through an Organocatalytic Oxa-conjugate Addition Reaction | Organic Letters
Focal application of an OX1R antagonist in the RTN and the medullary... | Download Scientific Diagram
Copper-Catalyzed Hydroamination of Oxa- and Azabenzonorbornadienes with Pyrazoles | The Journal of Organic Chemistry
Synthesis of α,α′-trans-Oxepanes through an Organocatalytic Oxa-conjugate Addition Reaction | Organic Letters
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Dynamic Kinetic Asymmetric Domino Oxa‐Michael/Carbocyclization by Combination of Transition‐Metal and Amine Catalysis: Catalytic Enantioselective Synthesis of Dihydrofurans - Lin - 2010 - Chemistry – A European Journal - Wiley Online Library
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![Organophotoredox-Catalyzed Intermolecular Oxa-[4+2] Cycloaddition Reactions | The Journal of Organic Chemistry](https://pubs.acs.org/cms/10.1021/acs.joc.9b01156/asset/images/medium/jo9b01156_0002.gif "Organophotoredox-Catalyzed Intermolecular Oxa-[4+2] Cycloaddition Reactions | The Journal of Organic Chemistry")
Organophotoredox-Catalyzed Intermolecular Oxa-[4+2] Cycloaddition Reactions | The Journal of Organic Chemistry
Synthesis of α,α′-trans-Oxepanes through an Organocatalytic Oxa-conjugate Addition Reaction | Organic Letters
Pea (@nxuzghsisskls) / Twitter
