DiastereoselectiveAddition of Racemic α-BorylOrganozinc Reagents to Aldimines

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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Publication Details

Journal
Organic Letters
Published
2026-08-14
DOI
https://doi.org/10.1021/acs.orglett.6c02969
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

DiastereoselectiveAddition of Racemic α-BorylOrganozinc Reagents to Aldimines

Miao Zhan, Xin An, Shuda Luo, Nan Wang et al.
Organic Letters
Organoboron and organosilicon chemistry
article

DiastereoselectiveAddition of Racemic α-BorylOrganozinc Reagents to Aldimines

Miao Zhan, Xin An, Shuda Luo, Nan Wang, Yuanhang Bai
article en

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.

Organic Letters
Northwestern Polytechnical University (CN), Northwestern Polytechnic University (US)
National Natural Science Foundation of China, Basic and Applied Basic Research Foundation of Guangdong Province
No poverty
Openalex Percentile: Top 18%
Organoboron and organosilicon chemistry
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