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Pd(II)‐catalyzed, Picolinamide‐aided sp2 γ−C−H Functionalization of Phenylglycinol: Access to γ−C−H Arylated, Alkylated and Halogenated Phenylglycinol Scaffolds
Asian Journal of Organic Chemistry ( IF 2.7 ) Pub Date : 2020-11-17 , DOI: 10.1002/ajoc.202000560
Prabhakar Singh 1 , Srinivasarao Arulananda Babu 1 , Yashika Aggarwal 1 , Pooja Patel 1
Affiliation  

We report the Pd(II)‐catalyzed picolinamide‐aided ortho‐C−H arylation‐, alkylation‐, and halogenation (sp2 γ−C−H functionalization) of phenylglycinol substrates. Phenylglycinols are remarkable building blocks and have found different applications in synthetic organic and medicinal chemistry. This work is a contribution towards the expansion of the library of phenylglycinol scaffolds and also substrate scope development by using the Pd(II)‐catalyzed bidentate directing group picolinamide‐aided C−H activation tactic.

中文翻译:

Pd(II)催化,吡啶甲酰胺辅助的sp2γ-CHF苯甘醇功能化:进入γ-CH酰化,烷基化和卤代的苯基甘醇支架

我们报告的钯(II) -催化的吡啶甲酰胺辅助-C-H arylation-,alkylation-,和卤化(SP 2 γ苯基甘氨醇基板的-C-H官能化)。苯甘氨醇是非凡的组成部分,在合成有机和药物化学中发现了不同的应用。这项工作是通过使用Pd(II)催化的二齿酸引导的吡咯啉酰胺辅助的CH活化策略来扩大苯基甘醇支架文库以及开发底物范围的。
更新日期:2021-01-18
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