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ChemInform Abstract: Supported Bifunctional Thioureas as Recoverable and Reusable Catalysts for Enantioselective Nitro‐Michael Reactions.

José M. Andrés, Miriam Ceballos, Alicia Maestro, Isabel Sanz, Rafaël Pedrosa

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Abstract

Abstract Four bifunctional thioureas supported on sulfonylpolystyrene resins are studied as catalysts in the stereoselective nitro‐Michael addition of various nucleophiles to trans‐β‐nitrostyrene derivatives.

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Abstract Four bifunctional thioureas supported on sulfonylpolystyrene resins are studied as catalysts in the stereoselective nitro‐Michael addition of various nucleophiles to trans‐β‐nitrostyrene derivatives.

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Available abstract

Abstract Four bifunctional thioureas supported on sulfonylpolystyrene resins are studied as catalysts in the stereoselective nitro‐Michael addition of various nucleophiles to trans‐β‐nitrostyrene derivatives.

Key concepts: Bifunctional, Chemistry, Nitro, Enantioselective synthesis, Nucleophile, Catalysis, Michael reaction, Stereoselectivity

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ChemInform Abstract: Supported Bifunctional Thioureas as Recoverable and Reusable Catalysts for Enantioselective Nitro‐Michael Reactions. — Research Paper | ScholarLens