氮丙啶
部分
对映选择合成
亲核细胞
磷化氢
化学
催化作用
锰
立体选择性
组合化学
立体化学
对称化
戒指(化学)
有机化学
作者
Syuzanna R. Harutyunyan,Chao Ni,Tizian‐Frank Ramspoth,Marta Castiñeira Reis
标识
DOI:10.1002/anie.202415623
摘要
Herein, we present the first catalytic asymmetric nucleophilic addition of diarylphosphines to 2H-azirines, facilitated by a chiral Mn(I) complex. This method not only provides access to novel class of derivatives of the aziridine core-a structural motif recognized for its antitumor and antibacterial properties-but also introduces a phosphine moiety alongside the generation of an NH moiety within a strained three-membered ring. The discovery of this new Mn(I) complex that both enables the reaction and induces stereoselectivity is pivotal, as it underscores the significant potential of this earth-abundant metal in advancing asymmetric catalysis.
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