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Efficient Synthesis of Novel Bridgehead-Substituted Bicyclo[3.2.1]octane-2,4-diones

Sebastian V. Wendeborn, Hannes Nussbaumer, Jürgen Schaetzer, Tammo Winkler

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Abstract

We report the efficient synthesis of bridgehead-substituted bicyclo[3.2.1]octane-2,4-diones. The key step in their construction is a highly efficient intramolecular [3+2] cycloaddition between a nitrile oxide and an olefin. The reductive ring cleavage of the resulting dihydroisoxazole provides the desired bridgehead-­substituted bicyclo[3.2.1]octane-2,4-diones.

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What this paper is about

We report the efficient synthesis of bridgehead-substituted bicyclo[3.2.1]octane-2,4-diones. The key step in their construction is a highly efficient intramolecular [3+2] cycloaddition between a nitrile oxide and an olefin. The reductive ring cleavage of the resulting dihydroisoxazole provides the desired bridgehead-­substituted bicyclo[3.2.1]octane-2,4-diones.

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Available abstract

We report the efficient synthesis of bridgehead-substituted bicyclo[3.2.1]octane-2,4-diones. The key step in their construction is a highly efficient intramolecular [3+2] cycloaddition between a nitrile oxide and an olefin. The reductive ring cleavage of the resulting dihydroisoxazole provides the desired bridgehead-­substituted bicyclo[3.2.1]octane-2,4-diones.

Key concepts: Bicyclic molecule, Octane, Chemistry, Nitrile, Cycloaddition, Olefin fiber, Intramolecular force, Ring (chemistry)

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