首页> 外文期刊>The Journal of Organic Chemistry >Aromatics to riquinanes. Synthesis and photoreaction of tricyclo[5.2.2.0~2.6]undecanes having an α-methoxy β,γ-unsaturated carbonyl chromophore
【24h】

Aromatics to riquinanes. Synthesis and photoreaction of tricyclo[5.2.2.0~2.6]undecanes having an α-methoxy β,γ-unsaturated carbonyl chromophore

机译:芳基到芳烃。具有α-甲氧基β,γ-不饱和羰基发色团的三环[5.2.2.0〜2.6]十一烷的合成与光反应

获取原文
获取原文并翻译 | 示例
       

摘要

A novel, general,k and stereoselective route for rapid creation of unctionalized, linearly fused cis:anti:cis triquinanes from aromatic precursors has been presented. Cycloaddition of 2-methoxy- spiro[cyclohexa-2,4-diene-6-2'-oxacyclopropan]one with various dienophiles nd the photochemical reaction of appropriately designed tricyclic systems, having an α-methoxy β,γ-enone chromophore upon triplet (~3T) sensitization, are the key elements of our approach.
机译:提出了一种新颖的,一般的,k的和立体选择性的途径,用于从芳香族前体中快速生成未取代的,线性稠合的顺式:反式:顺式三喹烷。 2-甲氧基-螺[环己-2,4-二烯-6-2'-氧杂环丙烷]酮与各种亲二烯物的环加成反应和适当设计的三环体系的光化学反应,三环结构上具有α-甲氧基β,γ-烯酮发色团(〜3T)敏感度是我们方法的关键要素。

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