Title of article
Studies on Development of Sufficiently Chemoselective N-Acylation Reagents: N-Acyl-N-(2,3,4,5,6-pentafluorophenyl)methanesulfonamides
Author/Authors
Kazuhiro Kondo، نويسنده , , Erika Sekimoto، نويسنده , , Junko Nakao، نويسنده , , Yasuoki Murakami، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2000
Pages
14
From page
5843
To page
5856
Abstract
A variety of storable N-acyl-N-(2,3,4,5,6-pentafluorophenyl)methanesulfonamides (4a–e) prepared from N-2,3,4,5,6-pentafluorophenylmethanesulfonamide (3), have been developed after systematic research on the structure–reactivity relationship and were found to serve as N-acylation reagents exhibiting sufficiently good chemoselectivity.
Keywords
alkoxycarbonylation , Amine , Sulfonamide , Protective group , chemoselective N-acylation reagent
Journal title
Tetrahedron
Serial Year
2000
Journal title
Tetrahedron
Record number
1081080
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