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ChemInform Abstract: CYCLOPENTANONES, XV. SYNTHESIS OF 1‐ALKYL (OR ARYL)‐2‐HYDROXY‐3‐OXOCYCLOPENTENES AND OF 1‐ALKYL (OR ARYL)‐3,5‐DIOXOCYCLOPENTENES

W. Van Brussel, M. Vandewalle

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Abstract

Abstract Die Reduktion der Tri= äthoxy‐cyclopentenone (I) mit Lithiumaluminiumhydrid in siedendem Tetrahydrofuran führt zu einem Gemisch aus 2‐Hydroxy‐cyclopentenonen (II) als Hauptprodukt und 3,5‐Dioxocyclopentenen (III).

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What this paper is about

Abstract Die Reduktion der Tri= äthoxy‐cyclopentenone (I) mit Lithiumaluminiumhydrid in siedendem Tetrahydrofuran führt zu einem Gemisch aus 2‐Hydroxy‐cyclopentenonen (II) als Hauptprodukt und 3,5‐Dioxocyclopentenen (III).

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Available abstract

Abstract Die Reduktion der Tri= äthoxy‐cyclopentenone (I) mit Lithiumaluminiumhydrid in siedendem Tetrahydrofuran führt zu einem Gemisch aus 2‐Hydroxy‐cyclopentenonen (II) als Hauptprodukt und 3,5‐Dioxocyclopentenen (III).

Key concepts: Alkyl, Aryl, Chemistry, Cyclopentenone, Tetrahydrofuran, Medicinal chemistry, Stereochemistry, Organic chemistry

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ChemInform Abstract: CYCLOPENTANONES, XV. SYNTHESIS OF 1‐ALKYL (OR ARYL)‐2‐HYDROXY‐3‐OXOCYCLOPENTENES AND OF 1‐ALKYL (OR ARYL)‐3,5‐DIOXOCYCLOPENTENES — Research Paper | ScholarLens