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March 26, 2026The Journal of Organic Chemistry

Free-Radical-Promoted β-C-H Functionalization of Simple Aliphatic Ketones, Esters, and Acids with Quinones

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Authors

JCJiaran CaoZWZheng WangYLYueyi Li

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Overview

This research demonstrates a free-radical reaction that enables β-C-H functionalization in aliphatic carbonyl compounds, suggesting a novel synthetic strategy.

Key Points

  • The study aims to develop a method for β-C-H functionalization of aliphatic ketones, esters, and acids using quinones.
  • Introduced a free-radical-promoted coupling reaction
  • Targeted simple aliphatic ketones, esters, and acids
  • Avoided the use of exogenous directing groups and transition metals
  • Achieved site-selective β-C-H functionalization
  • Facilitated the formation of β-C-C bonds
  • Provided a new strategy for the selective alkylation of quinones

Cite This Study

Cao et al. (2026) studied this question.

synapsesocial.com/papers/69c4ccc9fdc3bde4489185e3https://doi.org/10.1021/acs.joc.5c03182
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