Catalytic Asymmetric Synthesis of α-Alkenyl Quaternary Amino Acid Esters
Although chiral α-alkenyl quaternary amino acid derivatives have been extensively utilized in organic synthesis, the catalytic asymmetric synthesis of such compounds remains elusive. In this report, we present a highly efficient method for the direct introduction of an alkenyl group at the α carbon of an NH<sub>2</sub>-unprotected amino acid ester through a three-component reaction involving readily available aryl (alkenyl) bromide and allyl acetate, facilitated by chiral aldehyde/palladium co-catalysis. A diverse array of α-alkenyl quaternary amino acid esters featuring unconjugated π systems are generated in commendable yields and excellent enantioselectivities, and some of them are used for the synthesis of valuable building blocks.
Authors
- Chao-Xing Li
- Zhu‐Lian Wu (ORCID: https://orcid.org/0000-0001-8444-4028)
- Ya Wu (ORCID: https://orcid.org/0000-0002-9484-839X)
- Yanmin Huang (ORCID: https://orcid.org/0000-0002-9848-6461)
- Wei Wen
- Qi‐Xiang Guo (ORCID: https://orcid.org/0000-0002-0405-7958)
- Tian Cai
- Yong Li
Institutions
- Southwest University (CN)
- Smart Material (Germany) (DE)
- Chongqing University of Arts and Sciences (CN)
- Nanning Normal University (CN)
Publication Details
- Journal
- Organic Letters
- Published
- 2026-02-12
- DOI
- https://doi.org/10.1021/acs.orglett.6c00043
- Primary Topic
- Asymmetric Synthesis and Catalysis
- Type
- article
- Field-Weighted Citation Impact
- 0.00