Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5286373 | Tetrahedron Letters | 2005 | 4 Pages |
Abstract
Arylsulfamoyl imidazolium triflates, readily prepared from the corresponding chlorides, react with amines under neutral conditions to form arylsulfamides in high yields. This methodology, which contrasts with the slow and inefficient reactions of amines with arylsulfamoyl chlorides, is applied to the synthesis of arylsulfamide 3a, a bioisotere of muraglitazar.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Hyeon Kyu Lee, Miyeon Bang, Chwang Siek Pak,