t-BuOK/DMF促进的通过自由基过程实现吲哚酮的C-3位硫化反应

  • 王丽丽 ,
  • 张洲 ,
  • 王廷良 ,
  • 王兴兰 ,
  • 毛远湖 ,
  • 张吉泉
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  • 贵州医科大学贵州省化学合成药物研发利用工程技术研究中心,贵州医科大学药学院,贵阳,561113

收稿日期: 2024-03-11

  修回日期: 2024-04-18

  网络出版日期: 2024-05-11

t-BuOK/DMF-promoted C-3 sulfuration of oxindoles via a radical process

  • Wang Lili ,
  • Zhang Zhou ,
  • Wang Tingliang ,
  • Wang Xinglan ,
  • Mao Yuanhu ,
  • Zhang Jiquan
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  • Guizhou Provincial Engineering Technology Research Center for Chemical Drug R&D, College of Pharmacy, Guizhou Medical University, Guiyang, 561113, China

Received date: 2024-03-11

  Revised date: 2024-04-18

  Online published: 2024-05-11

摘要

本文发展了一种高效的吲哚酮的C-3位直接硫化反应。通过使用二硫化物作为硫化试剂,t-BuOK/DMF作为催化剂,一系列吲哚酮的C-3位硫化产物被成功合成。该方法具有较高的原子经济性、环境友好且底物适应范围广。

本文引用格式

王丽丽 , 张洲 , 王廷良 , 王兴兰 , 毛远湖 , 张吉泉 . t-BuOK/DMF促进的通过自由基过程实现吲哚酮的C-3位硫化反应[J]. 有机化学, 0 : 0 . DOI: 10.6023/cjoc202312024

Abstract

An efficient C-3 sulfuration of oxindoles has been developed. Using disulfide as the sulfurating agent, a wide range of sulfurated oxindoles have been synthesized under t-BuOK/DMF promoted conditions. The present method was highly atom economic, environmentally friendly and tolerated a broad scope of substrates.

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