首页> 外文期刊>Journal of Labelled Compounds and Radiopharmaceuticals >Synthesis of aryl (~(35)S)sulfones: Friedel-CrNts sulfonylation of aryl ethers with high specific activity (~(35)S)methanesulfonyl chloride
【24h】

Synthesis of aryl (~(35)S)sulfones: Friedel-CrNts sulfonylation of aryl ethers with high specific activity (~(35)S)methanesulfonyl chloride

机译:芳基(〜(35)S)砜的合成:具有高比活度(〜(35)S)甲磺酰氯的芳基醚的Friedel-CrNts磺酰化

获取原文
获取原文并翻译 | 示例
           

摘要

Lewis acid-assisted sulfonylation of anisole with [~(35)S]methanesulfonyl chloride Nforded high specific activity aryl [~(35)S]sulfones. Demethylation and treatment with triflic anhydride gave the versatile [~(35)S]triflate 1 in good overall yields. The [~(35)S]sulfone triflate could be further functionalized by catalyzed aminations, Stille couplings, and cyanation.
机译:路易斯酸辅助苯甲醚与[〜(35)S]甲磺酰氯的磺酰化Nforded高比活芳基[​​〜(35)S]砜。脱甲基并用三氟甲磺酸酐处理得到通用的[〜(35)S]三氟甲磺酸盐1,总收率良好。 [〜(35)S]砜三氟甲磺酸酯可通过催化胺化,斯蒂勒偶联和氰化进一步官能化。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号