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ChemInform Abstract: Organocatalysis for the Synthesis of Optically Active β‐Malonophosphonates.

Prashant B. Thorat, Santosh V. Goswami, Rupali L. Magar, Sudhakar R. Bhusare

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Abstract

Abstract Phospha—Michael addition of P(O—Et)3 to benzylidenemalononitriles (I) in the presence of a proline‐based organocatalyst represents one of the most straightforward routes for the synthesis of optically active β‐malonophosphonates (III) (13 examples).

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What this paper is about

Abstract Phospha—Michael addition of P(O—Et)3 to benzylidenemalononitriles (I) in the presence of a proline‐based organocatalyst represents one of the most straightforward routes for the synthesis of optically active β‐malonophosphonates (III) (13 examples).

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Available abstract

Abstract Phospha—Michael addition of P(O—Et)3 to benzylidenemalononitriles (I) in the presence of a proline‐based organocatalyst represents one of the most straightforward routes for the synthesis of optically active β‐malonophosphonates (III) (13 examples).

Key concepts: Chemistry, Optically active, Organocatalysis, Proline, Michael reaction, Combinatorial chemistry, Enantioselective synthesis, Organic chemistry

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