4.7 Article

Thiazolobenzyne: a versatile intermediate for multisubstituted benzothiazoles

期刊

CHEMICAL COMMUNICATIONS
卷 52, 期 75, 页码 11199-11202

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c6cc05112j

关键词

-

资金

  1. Platform for Drug Discovery, Informatics, and Structural Life Science from MEXT, Japan
  2. Platform for Drug Discovery, Informatics, and Structural Life Science from AMED, Japan
  3. CREST from JST, Japan
  4. JSPS KAKENHI [15H03118, 16H01133, 26350971]
  5. Cooperative Research Program of Network Joint Research Center for Materials and Devices
  6. CREST from AMED, Japan
  7. Grants-in-Aid for Scientific Research [15H03118, 26350971, 16H01133] Funding Source: KAKEN

向作者/读者索取更多资源

Thiazolobenzyne, which is a benzyne species fused with a thiazole ring, was efficiently generated via an iodine-magnesium exchange reaction of an ortho-iodoaryl triflate-type precursor using a trimethylsilylmethyl Grignard reagent as an activator. A wide range of arynophiles reacted efficiently with the thiazolobenzynes generated by this method to afford various multisubstituted benzothiazoles.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据