当前位置: X-MOL 学术Synlett › 论文详情
Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)
Construction of Benzylic Stereogenic Carbon Centers through Enantioselective Arylation Reactions
Synlett ( IF 2 ) Pub Date : 2017-10-20 , DOI: 10.1055/s-0036-1590923
Ren-Rong Liu 1 , Ren-Xiao Liang 1 , Yi-Xia Jia 1
Affiliation  

Compounds bearing chiral benzylic stereocenters are important and frequently occur in natural products and drug molecules. In this account, we discuss our recent results on the construction of ­benzylic stereogenic centers based on enantioselective arylation and related domino sequences, mainly including asymmetric Friedel–Crafts alkylation reactions and asymmetric Heck reactions. 1 Introduction 2 The Catalytic Asymmetric Friedel–Crafts Alkylation Reaction 2.1 Reactions of Electron-Deficient Alkenes 2.2 Reactions of Active Ketimines 2.3 Reactions of Nitrones 2.4 Reactions of Aziridines 3 The Asymmetric Heck Reaction 3.1 Dearomative Heck Reactions and Related Domino Sequences 3.2 Heck Reactions of in situ Formed Enamines 4 Conclusion and Outlook

中文翻译:

通过对映选择性芳基化反应构建苄基立体碳中心

带有手性苄基立体中心的化合物很重要,并且经常出现在天然产物和药物分子中。在这篇文章中,我们讨论了我们最近基于对映选择性芳基化和相关多米诺序列构建苄基立体中心的结果,主要包括不对称 Friedel-Crafts 烷基化反应和不对称 Heck 反应。1 引言 2 催化不对称 Friedel-Crafts 烷基化反应 2.1 缺电子烯烃的反应 2.2 活性酮亚胺的反应 2.3 硝酮的反应 2.4 氮丙啶的反应 3 不对称 Heck 反应 3.1 Deroromative Heck 反应和相关 Heck 序列中的 Heck 反应 2.形成烯胺 4 结论和展望
更新日期:2017-10-20
down
wechat
bug