Materials & Energyarticle2026-08-14

DiastereoselectiveAddition of Racemic α-BorylOrganozinc Reagents to Aldimines

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Abstract

Abstract The addition of alkylzinc reagents to imines is a key route to amines, but suffers from poor selectivity when racemic secondary alkylzincs are employed. Herein, we report a transition-metal-free diastereoselective addition of racemic α-boryl organozincs to aldimines, affording anti-β-aminoborons with good to excellent diastereoselectivities. Furthermore, Cu-catalyzed addition of racemic α-boryl organozincs to N-tert-butanesulfinyl aldimines afforded enantioenriched anti-β-aminoborons, preferentially delivering one of the four possible stereoisomers with high selectivity.

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View paper (DOI)OpenAlexOrganic LettersPublished 2026-08-14

Authors: Shuda Luo, Xin An, Yuanhang Bai, Nan Wang, Miao Zhan

Institutions: Northwestern Polytechnical University, Northwestern Polytechnic University