Construction of Quaternary Allylic Amino Acid Derivatives through Palladium-Catalyzed Allylic Alkylation Reaction of Azlactones with Vinyl Aziridine

被引:1
作者
Huang, Ke-Xin [1 ]
Chen, Zhao-Yang [1 ]
Liu, Xue-Guo [1 ]
Ye, Hong-Yong [1 ]
Gao, Wen-Chao [2 ]
机构
[1] Nanyang Inst Technol, Sch Biol & Chem Engn, Nanyang 473000, Henan, Peoples R China
[2] Nanyang Normal Univ, Sch Chem & Pharmaceut Engn, Nanyang 473000, Henan, Peoples R China
来源
SYNTHESIS-STUTTGART | 2022年 / 54卷 / 20期
关键词
allylic alkylation; quaternary allylic amino acid derivatives; Pd-catalyzed; vinyl aziridine; azlactones; DYNAMIC KINETIC RESOLUTION; ASYMMETRIC-SYNTHESIS; ENANTIOSELECTIVE SYNTHESIS; GAMMA-ADDITIONS; DESIGN; DIHYDROCOUMARINS; CYCLOADDITION; ACCESS; HETEROCYCLES; TERTIARY;
D O I
10.1055/a-1878-8084
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A highly efficient Pd-catalyzed allylic alkylation reaction of azlactones with vinyl aziridine has been achieved for the first time to access functionalized quaternary allylic amino acid derivatives (17 examples, up to 89% yield and 80% ee). Moreover, the broad scope and easy transformations of the products reinforce the value of this approach, which can enrich the chemistry of quaternary allylic amino acid derivatives.
引用
收藏
页码:4495 / 4502
页数:8
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