...
首页> 外文期刊>Synthesis: International Journal of Methods in Synthetic Organic Chemistry >Alkyl Nitrites: Novel Reagents for One-Pot Synthesis of 3,5-Disubstituted Isoxazoles from Aldoximes and Alkynes
【24h】

Alkyl Nitrites: Novel Reagents for One-Pot Synthesis of 3,5-Disubstituted Isoxazoles from Aldoximes and Alkynes

机译:烷基亚硝酸盐:新型试剂,可从醛糖肟和炔烃一次合成3,5-二取代异恶唑

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

An efficient, one-pot approach has been described for the synthesis of 3,5-disubstituted isoxazoles from substituted aldoximes (mixture of E and Z) and alkynes, using alkyl nitrites under conventional heating conditions. The key nitrile oxide intermediates that are required for the synthesis of isoxazoles are formed by treatment of substituted aldoxime with either tert-butyl nitrite or isoamyl nitrite. The generated nitrile oxides underwent in situ [3+2] dipolar cycloaddition to the substituted alkynes to give 3,5-disubstituted isoxazoles regioselectively in high to excellent yields. The developed synthetic methodology was applied for the synthesis of a previously reported potent hDGAT1 inhibitor.
机译:已经描述了一种有效的一锅法,该方法用于在常规加热条件下使用烷基亚硝酸盐从取代的醛肟(E和Z的混合物)和炔烃合成3,5-二取代的异恶唑。合成异恶唑所需的关键腈氧化物中间体是通过用亚硝酸叔丁酯或亚硝酸异戊酯处理取代的醛肟而形成的。生成的腈氧化物在取代的炔烃上进行原位[3 + 2]偶极环加成反应,以高选择性或极高的产率选择性地生成3,5-二取代的异恶唑。已开发的合成方法用于合成先前报道的有效hDGAT1抑制剂。

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