Synthesis of Diver γ-Aryl-β-ketoesters via Ary

更新时间:2023-05-15 10:33:26 阅读: 评论:0

蛊师Synthesis of Diver γ-Aryl-β-ketoesters via Aryne Intermediates Generated by C-C Bond Cleavage.
期刊名称: Organic letters
毕飞宇
详细的英语作者: Keisuke,Uchida,Yasunori,Minami,Suguru,Yoshida,Takamitsu,Hosoya
作者机构: Laboratory
年份: 2019年
红烧小鸡腿
大理有什么好玩的地方景点推荐期号: 第22期
摘要:A synthetic method for diver γ-aryl-β-ketoesters through γ-aryl-β-ketoester-type arynes triggered by C-C bond cleavage has been developed. The Mukaiyama aldol reaction of 6-(triflyloxy)benzocyclobutenones with ketene silyl acetals and subquent treatment of resulting 6-(triflyloxy)benzocyclobutenols with a ba triggered the efficient generation of γ-aryl-β-ketoester-type arynes, which reacted with various arynophiles to provide a wide range of γ-aryl-β-ketoesters. The synthetic utility of the method was demonstrated by the synthesis of an analog of ALK inhibitor.一节课的英文
班级现状分析>学蒸馒头
内容由中国教育图书进出口有限公司引进

本文发布于:2023-05-15 10:33:26,感谢您对本站的认可!

本文链接:https://www.wtabcd.cn/fanwen/fan/89/899160.html

版权声明:本站内容均来自互联网,仅供演示用,请勿用于商业和其他非法用途。如果侵犯了您的权益请与我们联系,我们将在24小时内删除。

标签:好玩   教育   图书   景点   推荐
相关文章
留言与评论(共有 0 条评论)
   
验证码:
推荐文章
排行榜
Copyright ©2019-2022 Comsenz Inc.Powered by © 专利检索| 网站地图