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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).
DOI10.1039/d0cc06055k
发表期刊CHEMICAL COMMUNICATIONS
ISSN1359-7345
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