首页> 外文期刊>Chemistry: A European journal >alpha,beta-Unsaturated Gold(I) Carbenes by Tandem Cyclization and 1,5-Alkoxy Migration of 1,6-Enynes: Mechanisms and Applications
【24h】

alpha,beta-Unsaturated Gold(I) Carbenes by Tandem Cyclization and 1,5-Alkoxy Migration of 1,6-Enynes: Mechanisms and Applications

机译:通过串联环化和1,6-烯炔的1,5-烷氧基迁移形成α,β-不饱和金(I)卡宾烷:机理与应用

获取原文
获取原文并翻译 | 示例
           

摘要

1,6-Enynes bearing OR groups at the propargyl position generate alpha,beta-unsaturated gold(I)-carbenes/ gold(I) stabilized allyl cations that can be trapped by alkenes to form cyclopropanes or 1,3-diketones to give products of alpha-alkylation. The best migrating group is p-nitrophenyl ether, which leads to the corresponding products without racemization. Thus, an improved formal synthesis of (+)-schisanwilsonene A has been accomplished. The different competitive reaction pathways have been delineated computationally.
机译:在炔丙基位置带有OR基团的1,6-Enynes生成α,β-不饱和的金(I)-碳烯/金(I)稳定的烯丙基阳离子,可被烯烃捕获以形成环丙烷或1,3-二酮,得到产物α-烷基化。最佳的迁移基团是对硝基苯醚,可得到相应的产物而没有外消旋作用。因此,已经完成了(+)-schisanwilsonene A的改进的形式合成。不同的竞争反应途径已经在计算上进行了描述。

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