Chirality memory of α-methylene-π-allyl iridium species. Issue 35 (10th August 2021)

• Record Type: Journal Article
• Authors: Cui, Yifan; Zhai, Yizhan; Xiao, Junzhe; Li, Can; Zheng, Wei-Feng; Huang, Chaofan; Wu, Guolin; Qin, Anni; Lin, Jie; Liu, Qi; Wang, Huanan; Wu, Penglin; Xu, Haibo; Zheng, Yangguangyan; Ma, Shengming
• Is Part Of: Chemical science. Volume 12:Issue 35(2021)
• Page Start: 11831
• Page End: 11838
• Publication Date: 2021-08-10
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/d1sc02636d
• Languages: English
• ISSNs: 2041-6520

Abstract

Abstract : Chirality is one of the most important types of steric information in nature. Abstract : Chirality is one of the most important types of steric information in nature. In addition to central chirality, axial chirality has been catching more and more attention from scientists. However, although much attention has recently been paid to the creation of axial chirality and the chirality transfer of allenes, no study has been disclosed as to the memory of such an axial chirality. The reason is very obvious: the chiral information is stored over three carbon atoms. Here, the first example of the memory of chirality (MOC) of allenes has been recorded, which was realized via an optically active alkylidene-π-allyl iridium intermediate, leading to a highly stereoselective electrophilic allenylation with amines. Specifically, we have established the transition metal-mediated highly stereoselective 2, 3-allenylation of amines by using optically active 2, 3-allenyl carbonates under the catalysis of a nonchiral iridium(iii ) complex. This method is compatible with sterically bulky and small substituents on both amines and 2, 3-allenyl carbonates and furnishes the desired optically active products with a high efficiency of chirality transfer. Further mechanistic experiments reveal that the isomerization of the optically active alkylidene-π-allyl iridium intermediate is very slow.