The crystal structures of aromatic compounds and its reduction product C2H11N3O2S was investigated. The reduction of the compound reportedly lead to the corresponding benzyl analogue. The structural evidence demonstrated that the product of the reaction were isomer. The crystal structure established that the reduction product possesses an H atom on the exocyclic N atom forming hydrogen-bonded dimers over centers of inversion.
|Journal||Acta crystallographica Section C: Crystal Structure communications|
|Publication status||Published - 1 Feb 2002|