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α,β-不饱和γ-丁内酰胺以有机催化方式进行不对称共轭加成反应时的直接β-选择性。

Direct β-selectivity of α,β-unsaturated γ-butyrolactam for asymmetric conjugate additions in an organocatalytic manner.

作者信息

Zhong Yuan, Hong Sihua, Cai Zhengjun, Ma Shixiong, Jiang Xianxing

机构信息

School of Pharmaceutical Sciences, Sun Yat-Sen University Guangzhou 510006 China

Key Laboratory of Preclinical Study for New Drugs of Gansu Province, School of Basic Medical Sciences, Lanzhou University Lanzhou 730000 China.

出版信息

RSC Adv. 2018 Aug 14;8(51):28874-28878. doi: 10.1039/c8ra05264f.

Abstract

The β-selective asymmetric addition of γ-butyrolactam with cyclic imino esters catalyzed by a bifunctional chiral tertiary amine has been developed, which provides an efficient access to optically active β-position functionalized pyrrolidin-2-one derivatives in both high yield and enantioselectivity (up to 78% yield and 95 : 5 er). This is the first catalytic method to access chiral β-functionalized pyrrolidin-2-one a direct organocatalytic approach.

摘要

已经开发出一种由双功能手性叔胺催化的γ-丁内酰胺与环状亚胺酯的β-选择性不对称加成反应,该反应能以高收率和对映选择性(高达78%的收率和95:5的对映体过量)高效合成具有光学活性的β-位官能化吡咯烷-2-酮衍生物。这是获得手性β-官能化吡咯烷-2-酮的第一种催化方法——一种直接的有机催化方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/194e/9084493/463b13e4b292/c8ra05264f-s1.jpg

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