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• W4213303380 abstract "Abstract A new class of chiral 2,2′‐bipyridine ligands, SBpy, featuring minimized short‐range steric hindrance and structural tunability was rationally designed and developed, and the effectiveness was demonstrated in the first highly enantioselective Ni‐catalyzed addition of aryl halides to aldehydes. In comparison with known approaches using preformed aryl metallic reagents, this reaction is more step‐economical and functional group tolerant. The reaction mechanism and a model of stereocontrol were proposed based on experimental and computational results." @default.
• W4213303380 created "2022-02-24" @default.
• W4213303380 creator A5007322337 @default.
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• W4213303380 creator A5051182441 @default.
• W4213303380 creator A5051427074 @default.
• W4213303380 creator A5090654861 @default.
• W4213303380 date "2022-02-26" @default.
• W4213303380 modified "2023-10-16" @default.
• W4213303380 title "Design and Synthesis of Tunable Chiral 2,2′‐Bipyridine Ligands: Application to the Enantioselective Nickel‐Catalyzed Reductive Arylation of Aldehydes" @default.
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• W4213303380 doi "https://doi.org/10.1002/ange.202117843" @default.
• W4213303380 hasPublicationYear "2022" @default.

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