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Ferricyanide oxidation of 1-substituted pentaphenylpyridinium salts. A novel route to 1-substituted 2,3,4,5-tetraphenylpyrroles

Stanislav Böhm, Hanuš Slavík, Josef Kuthan

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Abstract

Oxidation of 1-substituted 2,3,4,5,6-pentaphenylpyridinium salts Ia-Ij by potassium ferricyanide in an alkaline medium yields the corresponding 1-substituted 2,3,4,5-tetraphenylpyrroles in 68 to 76% yields. The selectivity of the reaction is discussed.

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Oxidation of 1-substituted 2,3,4,5,6-pentaphenylpyridinium salts Ia-Ij by potassium ferricyanide in an alkaline medium yields the corresponding 1-substituted 2,3,4,5-tetraphenylpyrroles in 68 to 76% yields. The selectivity of the reaction is discussed.

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Available abstract

Oxidation of 1-substituted 2,3,4,5,6-pentaphenylpyridinium salts Ia-Ij by potassium ferricyanide in an alkaline medium yields the corresponding 1-substituted 2,3,4,5-tetraphenylpyrroles in 68 to 76% yields. The selectivity of the reaction is discussed.

Key concepts: Potassium ferricyanide, Ferricyanide, Selectivity, Chemistry, Potassium, Inorganic chemistry, Combinatorial chemistry, Medicinal chemistry

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Ferricyanide oxidation of 1-substituted pentaphenylpyridinium salts. A novel route to 1-substituted 2,3,4,5-tetraphenylpyrroles — Research Paper | ScholarLens