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◆ Organic letters2026-08-14

Copper-Catalyzed Ring-Opening Addition of Cyclopropanols to Imines: Enantioselective Synthesis of γ-Sulfonamido Ketones.

Zhiyong Chi, Xiaoling Cheng, Longxiao Chi, Shaofeng Wu, Guo Tang, Lei Gong

原始摘要(英文原文)· Original abstract
Chiral γ-amino ketones are vital scaffolds, yet catalytic asymmetric synthesis is constrained by side reactions and remote stereocontrol. We report a copper-catalyzed addition of cyclopropanols to N-sulfonyl imines that leverages ring strain for ring opening. This mechanistically distinct platform enables efficient construction of quaternary stereocenters, affording products in up to 98% yield and 93% ee.
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Copper-Catalyzed Ring-Opening Addition of Cyclopropanols to Imines: Enantioselective Synthesis of γ-Sulfonamido Ketones. — 科研速览 Science Skim