期刊
ORGANIC LETTERS
卷 25, 期 19, 页码 3402-3406出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.3c00927
关键词
-
A decarboxylative amidation of aryl/heteroarylacetic acids by reaction with NHS and tert-butyl nitrite has been reported, which offers a convenient method for the synthesis of aliphatic and (hetero)aromatic amides. Mechanistic studies reveal a previously unexplored pathway involving traceless alpha-functionalized benzylic radicals for the formation of activated ester, followed by one-pot reaction with amines to form amides. The gram-scale synthesis of Moclobemide demonstrates the practical applicability of this method.
Unlike conventional amide synthesis, a decarboxylative amidation of aryl/heteroarylacetic acids by reaction with NHS and tert-butyl nitrite has been reported to afford both aliphatic and (hetero)aromatic amides in satisfactory yields. Mechanistic studies revealed a previously unexplored pathway for the formation of an activated ester through the generation and subsequent reactions of traceless alpha-functionalized benzylic radicals, which upon subsequent one-pot reaction with amines form the amides. A gram-scale synthesis of Moclobemide indicates the practical applicability.
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。
推荐
暂无数据