81640-25-7Relevant articles and documents
Rearrangement with Oxygen-Insertion in Azabicyclic Hydroxylamine Derivatives
Heesing, Albert,Herdering, Wilhelm,Henkel, Gerald,Krebs, Bernt
, p. 1107 - 1117 (2007/10/02)
N-Hydroxy-2-azabicyclohept-5-ene (1) is rearranged to the oxaazabicyclic compounds 3,4, and 8 by the reaction with either tosyl or benzoyl chloride.The structure of 3 was proved by X-ray analysis.Experiments with tosyl chloride as well product
SAUERSTOFF-INSERTION BEI DER UMLAGERUNG VON 2-AZA-BICYCLOHEPT-2-EN-DERIVATEN
Heesing, A.,Herdering, W.
, p. 4675 - 4678 (2007/10/02)
N-Acyclation of N-hydroxy-2-azabicyclohept-2-ene causes rearrangement to oxa-aza-bicycles (7, 8) by insertion of the hydroxalamine oxygen into the heterocyclic system.The mechanism is elucidated.