KMS Chongqing Institute of Green and Intelligent Technology, CAS
Bench-stable imine surrogates for the one-pot and catalytic asymmetric synthesis of alpha-amino esters/ketones | |
Xu, Huacheng1; Nazli, Adila1; Zou, Cheng1; Wang, Zhi-Peng2; He, Yun1 | |
2020-11-25 | |
摘要 | N,O-Bis(tert-butoxycarbonyl)hydroxylamines are readily accessible as imine surrogates, which are bench stable and could quantitatively generate the corresponding imines for in situ applications. An unpresented catalytic asymmetric method for the synthesis of alpha-amino esters and ketones from novel imine surrogates, N,O-bis(tert-butoxycarbonyl)hydroxylamines, as well as its preliminary mechanistic studies are reported. A variety of optically enriched products were obtained in excellent yields and enantioselectivities (up to 99% yield and >99% ee). |
DOI | 10.1039/d0cc06055k |
发表期刊 | CHEMICAL COMMUNICATIONS |
ISSN | 1359-7345 |
卷号 | 56期号:91页码:14243-14246 |
通讯作者 | Wang, Zhi-Peng(wangzhipeng@cigit.ac.cn) ; He, Yun(yun.he@cqu.edu.cn) |
收录类别 | SCI |
WOS记录号 | WOS:000590124000020 |
语种 | 英语 |