New Chiral Bifunctional Iminophosphorane Squaramide Organocatalysts: Synthesis and Application in the Enantioselective Michael Addition

Abstract The design and the synthesis of new enantiopure squaramide-based bifunctional iminophosphorane catalysts are reported. Starting from readily available starting materials, such as squarate and (S)-tert-leucinol, the synthetic approach involved the construction of a squaramide featuring an azide group, as precatalyst, which is easily stored, not sensible to moisture, and highly manageable. The chiral iminophosphorane organocatalysts (generated in situ by simple addition of a phosphine to the azide) were tested in the enantioselective Michael addition of α-nitro esters to enones and promoted the reaction in up to 90% yield and 60% e.e. The products are valuable precursors of α,α-disubstituted amino acids, important building blocks in the preparation of highly functionalized molecules. The synthesis of an α-methyl-substituted proline derivative was demonstrated.

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Journal
Synthesis
Published
2025-12-26
DOI
https://doi.org/10.1055/a-2779-1084
Primary Topic
Asymmetric Synthesis and Catalysis
Type
article
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article

New Chiral Bifunctional Iminophosphorane Squaramide Organocatalysts: Synthesis and Application in the Enantioselective Michael Addition

Laura Raimondi, Maurizio Benaglia, Alessandra Puglisi, Francesca Franco et al.
Synthesis
Asymmetric Synthesis and Catalysis
article

New Chiral Bifunctional Iminophosphorane Squaramide Organocatalysts: Synthesis and Application in the Enantioselective Michael Addition

Laura Raimondi, Maurizio Benaglia, Alessandra Puglisi, Francesca Franco, Patricia Camarero Gonzales, Rabbani Wafda
article en

Abstract

Abstract The design and the synthesis of new enantiopure squaramide-based bifunctional iminophosphorane catalysts are reported. Starting from readily available starting materials, such as squarate and (S)-tert-leucinol, the synthetic approach involved the construction of a squaramide featuring an azide group, as precatalyst, which is easily stored, not sensible to moisture, and highly manageable. The chiral iminophosphorane organocatalysts (generated in situ by simple addition of a phosphine to the azide) were tested in the enantioselective Michael addition of α-nitro esters to enones and promoted the reaction in up to 90% yield and 60% e.e. The products are valuable precursors of α,α-disubstituted amino acids, important building blocks in the preparation of highly functionalized molecules. The synthesis of an α-methyl-substituted proline derivative was demonstrated.

SynthesisVol. 58(07)
University of Milan (IT)
Openalex Percentile: Top 33%
Asymmetric Synthesis and Catalysis
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