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Woollins’ reagent promotes selective reduction of α,β-unsaturated thiazo and selenazolidinones

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Abstract In this work we describe the Woollins’ reagent as useful for the selective reduction of the double bond of 2-α,β-unsaturated thiazo and selenazolidinones. The reaction took place in toluene… Click to show full abstract

Abstract In this work we describe the Woollins’ reagent as useful for the selective reduction of the double bond of 2-α,β-unsaturated thiazo and selenazolidinones. The reaction took place in toluene at room temperature to give the corresponding saturated heterocycles in good yields, eleven examples are given. The scope of the reaction is also discussed, being essential the conjugated ester to the double bond.

Keywords: selective reduction; woollins reagent; thiazo selenazolidinones; reagent promotes; unsaturated thiazo

Journal Title: Tetrahedron Letters
Year Published: 2017

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