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March 14, 2026Organic Letters0 citations

para -Selective C–H Arylation and Alkylation of N -Arylhydroxylamines

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RJRui-Qiang JiaoJPJingtai PeiZXZhenguo Xi

Key Points

  • This research focuses on developing a method for para-selective C-H functionalization.
  • Utilized fluorosulfuryl imidazolium triflate for direct para-selective C-H arylation and alkylation.
  • Examined various substrate scopes and functional group adaptations.
  • Achieved para-selective functionalization under mild conditions.
  • Demonstrated the method's practical utility for scalable production and further modifications of products.

Abstract

The direct para-selective functionalization of arenes is difficult under mild conditions without the use of directing groups and transition-metal catalysts. Here we present a fluorosulfuryl imidazolium triflate-mediated direct para-selective C-H arylation and alkylation of N-arylhydroxylamines. This protocol exhibits a broad substrate scope and great functional-group adaptability. Moreover, the potential for scalable production and the feasibility of further modifications of the products showcase the practical utility of this method in synthetic applications.

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Cite This Study

Jiao et al. (2026) studied this question.

synapsesocial.com/papers/69b4ba0818185d8a39802744https://doi.org/10.1021/acs.orglett.6c00585
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