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.
Authors
- Miao Zhan (ORCID: https://orcid.org/0000-0002-6492-5104)
- Xin An (ORCID: https://orcid.org/0009-0002-7544-1452)
- Shuda Luo
- Nan Wang
- Yuanhang Bai
Institutions
- Northwestern Polytechnical University (CN)
- Northwestern Polytechnic University (US)
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
Funders
- National Natural Science Foundation of China
- Basic and Applied Basic Research Foundation of Guangdong Province