941715-62-4Relevant articles and documents
2-aminophenols containing electron-withdrawing groups from N -Aryl hydroxylamines
Porzelle, Achim,Cooper, Anthony W.J.,Woodrow, Michael D.,Tomkinson, Nicholas C.O.
experimental part, p. 2471 - 2473 (2010/11/18)
Reaction of substituted N-aryl hydroxylamines with methanesulfonyl chloride, p-toluenesulfonyl chloride, or trifluoromethanesulfonic anhydride under basic conditions leads to the rearranged 2-aminophenols (45-94%). The overall reaction sequence can be per
Facile synthesis of benzamides to mimic an α-helix
Ahn, Jung-Mo,Han, Sun-Young
, p. 3543 - 3547 (2008/02/06)
A new α-helix mimetic was designed by using a benzamide as a rigid scaffold. It presents three functional groups corresponding to side chains of amino acids found at the i, i + 4, and i + 7 positions of an ideal α-helix, which are displayed on the same he