e.g. Filippa Pettersson or Cancer Res. 75(6) , 1102-12, (2015) or 10.1002/anie.201600521
Base-induced rearrangement of the O-methanesulphonyl derivatives of N-(alkylphenylphosphinoyl) hydroxylamines. Highly selective migration of the phenyl group
MJP Harger, A Smith
Index: Harger, Martin J. P.; Smith, Adrian Journal of the Chemical Society, Chemical Communications, 1984 , # 17 p. 1140 - 1141
The N-(alkylphenylphosphinoyl)-O-methanesulphonylhydroxylamines RPhP(0)NHOS02Me (R = Me, Et, or Pri) react readily with MeNH2 or NaOMe-MeOH to give products resulting from phenyl, but not alkyl, migration. ... N-( Diphenylphosphinoyl) hydroxylamine (2 , R = Ph) and some of its derivatives have recently been described.' The 0-methanesulphonate (3, R = Ph) is of particular interest because of its ready base-induced rearrangement; eg with NaOMe ...