Synlett 2000; 2000(3): 427
DOI: 10.1055/s-2000-6546
letter
© 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.

Chlorosulfonyl Isocyanate

Jean-François Cavalier*
  • *Laboratoire de Chimie Organique, Bât. Lavoisier, Université Catholique de Louvain, Place Louis Pasteur 1, B-1348 Louvain-la-Neuve, Belgium
Further Information

Publication History

Publication Date:
31 December 2000 (online)

Chlorosulfonyl isocyanate (CSI), is known as the strongest biselectrophile. It is very useful in many synthetic transformations and in the synthesis of various heterocyclic systems.

CSI presents two sites of attack by nucleophiles: at the SO2 group and at the C=O function leading then, to N-sulfonylisocyanate and N-chlorosulfonyl derivatives, respectively, which can be easily functionalized by reaction with water, alcohol or amine. Furthermore, cycloaddition reactions to the C=N double bond of the isocyanate function can also occur.

    >