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ChemInform Abstract: Triplex‐Catalyzed Diels‐Alder and (2 + 2)Cycloaddition Reactions of Enol Ethers and Ketene Acetals.

Nihat Akbulut, Gary B. Schuster

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Abstract

Abstract Cyclohexadiene (I) undergoes photochemical reaction with the silyl enol ethers (IIa) and (IIb) or the ketene acetal (IIc) in the presence of sensitizers such as 9,10‐dicyanoanthracene to form the bicyclooctenes (III) and (IV).

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What this paper is about

Abstract Cyclohexadiene (I) undergoes photochemical reaction with the silyl enol ethers (IIa) and (IIb) or the ketene acetal (IIc) in the presence of sensitizers such as 9,10‐dicyanoanthracene to form the bicyclooctenes (III) and (IV).

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Available abstract

Abstract Cyclohexadiene (I) undergoes photochemical reaction with the silyl enol ethers (IIa) and (IIb) or the ketene acetal (IIc) in the presence of sensitizers such as 9,10‐dicyanoanthracene to form the bicyclooctenes (III) and (IV).

Key concepts: Ketene, Chemistry, Enol, Acetal, Silylation, Cycloaddition, Catalysis, Enol ether

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ChemInform Abstract: Triplex‐Catalyzed Diels‐Alder and (2 + 2)Cycloaddition Reactions of Enol Ethers and Ketene Acetals. — Research Paper | ScholarLens