Catalytic asymmetric Payne oxidation under the catalysis of P-spiro chiral triaminoiminophosphorane: application to the synthesis of N-sulfonyl oxaziridines |
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Authors: | Daisuke Uraguchi Ryosuke Tsutsumi Takashi Ooi |
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Affiliation: | 1. Institute of Transformative Bio-Molecules (WPI-ITbM) and Department of Applied Chemistry, Graduate School of Engineering, Nagoya University, Furo-cho B2-3(611), Chikusa, Nagoya 464-8603, Japan;2. CREST, Japan Science and Technology Agency (JST), Chikusa, Nagoya 464-8603, Japan |
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Abstract: | The studies on the development of a highly enantioselective oxidation of N-sulfonyl imines with hydrogen peroxide–trichloroacetonitrile system utilizing P-spiro chiral triaminoiminophosphoranes as an organic base catalyst are detailed. This method is general and scalable, and exhibits unique chemoselectivity, providing a practical stereoselective route to structurally diverse N-sulfonyl oxaziridines. The mechanistic investigations reveal that the reaction proceeds through the Payne-type oxidation pathway. The synthetic utility of the optically active N-sulfonyl oxaziridines as versatile organic oxidants and chiral building blocks is also demonstrated. |
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Keywords: | Asymmetric catalysis Hydrogen peroxide Imine Organocatalysis Oxaziridine |
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