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ChemInform Abstract: Formation of Bicyclo(3.2.1)octane, Bicyclo(4.2.1)nonane, and Bicyclo‐(3.3.1)nonane by Transannular Radical Cyclizations.

Finlay MacCorquodale, John C. Walton

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Abstract

Abstract Cycloalkenylmethyl radicals, generated from the bromomethylcycloalkenes (I) by photolytically‐induced hydride reduction, undergo intramolecular ring closure to form the bicycloalkanes (IIIa) or (IVb) as the main products.

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What this paper is about

Abstract Cycloalkenylmethyl radicals, generated from the bromomethylcycloalkenes (I) by photolytically‐induced hydride reduction, undergo intramolecular ring closure to form the bicycloalkanes (IIIa) or (IVb) as the main products.

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Available abstract

Abstract Cycloalkenylmethyl radicals, generated from the bromomethylcycloalkenes (I) by photolytically‐induced hydride reduction, undergo intramolecular ring closure to form the bicycloalkanes (IIIa) or (IVb) as the main products.

Key concepts: Bicyclic molecule, Nonane, Chemistry, Octane, Intramolecular force, Ring (chemistry), Bridged compounds, Medicinal chemistry

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ChemInform Abstract: Formation of Bicyclo(3.2.1)octane, Bicyclo(4.2.1)nonane, and Bicyclo‐(3.3.1)nonane by Transannular Radical Cyclizations. — Research Paper | ScholarLens