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Facile Direct Coupling Reactions of MOM-protected Benzylic Alcohols Using Aluminum Chloride
Bulletin of the Korean Chemical Society ( IF 1.7 ) Pub Date : 2021-07-30 , DOI: 10.1002/bkcs.12358
Tien Tan Bui 1 , Hee‐Kwon Kim 1, 2
Affiliation  

MOM group is one of the most commonly used protecting groups for alcohols. This study describes novel direct functionalization of the MOM-protected benzylic alcohols. Preparation of allylic compounds from benzyl MOM ethers was successfully achieved by utilization of allyltrimethylsilane and AlCl3. In addition, direct azidation of benzyl MOM ethers using TMSN3 was successful carried out under AlCl3-mediated reaction conditions. These results demonstrate that this novel synthetic procedure is a promising approach to direct functionalization of MOM-protected alcohols including allylation and azidation.

中文翻译:

使用氯化铝进行 MOM 保护的苯甲醇的简便直接偶联反应

MOM 基团是最常用的醇类保护基团之一。本研究描述了 MOM 保护的苯甲醇的新型直接功能化。利用烯丙基甲基硅烷和AlCl 3成功地从苄基MOM醚制备烯丙基化合物。此外,在AlCl 3介导的反应条件下,使用TMSN 3成功地进行了苄基MOM 醚的直接叠氮化。这些结果表明,这种新的合成程序是一种有前途的方法,可以直接将 MOM 保护的醇官能化,包括烯丙基化和叠氮化。
更新日期:2021-09-23
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