Synthesis 1989; 1989(5): 394-395
DOI: 10.1055/s-1989-27263
communication
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

Ein bequemes Eintopfverfahren zur Synthese von 1,2-Benzisothiazol-1,1-dioxiden

D. Hellwinkel* , R. Karle
  • *Organisch-Chemisches Institut der Universitát Heidelberg, Im Neuenheimer Feld 270, D-6900 Heidelberg, Federal Republic of Germany
Further Information

Publication History

Publication Date:
17 September 2002 (online)

A Facile One-Pot Procedure for the Synthesis of 1,2-Benzisothiazole 1,1-Dioxides ortho-Lithiated N,N-diphenylbenzenesulfonamides 6 react with aromatic nitriles and N,N-dimethylcarbamonitrile, respectively, to give directly the corresponding 3-substituted 1,2-benzisothiazole-1,1-dioxides 8a-f. Other cyano compounds only transfer the cyano group or its ligands to generate the o-substituted benzenesulfonamides 9a-d.

    >