首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Stereoselective intramolecular hetero Diels-Alder reactions of l-oxa-l,3-butadienes:a novel approach for the synthesis of complex annulated uracils
【24h】

Stereoselective intramolecular hetero Diels-Alder reactions of l-oxa-l,3-butadienes:a novel approach for the synthesis of complex annulated uracils

机译:L-氧杂-1,3-丁二烯的立体选择性分子内杂Diels-Alder反应:合成复杂环状尿嘧啶的新方法

获取原文
获取原文并翻译 | 示例
           

摘要

The intramolecular hetero Diels-Alder reactions of l-oxa-l,3-butadienes 4,obtained from salicylaldehyde 1 via O-allyl-ation followed by Knoevenagel condensation with barbituric acids 3 in the presence of hydrochloric acid as catalyst,affords the tetracyclic uracil derivatives 5 and 6 in a Stereoselective manner and high overall yields.
机译:由水杨醛1经由O-烯丙基化后由Knoevenagel与巴比妥酸3的Knoevenagel缩合在盐酸作为催化剂的情况下获得的1-氧杂-1,3-丁二烯4的分子内杂Diels-Alder反应以立体选择性方式和高总收率得到衍生物5和6。

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