Synlett 1994; 1994(7): 539-541
DOI: 10.1055/s-1994-22921
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.

Cycloaddition of Chlorosulfonyl Isocyanate to Sugar Vinyl Ethers

Z. Kałuża* , W. Abramski, C. Bełżecki, J. Grodner, D. Mostowicz, R. Urbański, M. Chmielewski
  • *Institute of Organic Chemistry, Polish Academy of Sciences, 01-224 Warsaw, Poland
Further Information

Publication History

Publication Date:
18 September 2002 (online)

Storage of chlorosulfonyl isocyanate over potassium, sodium or calcium carbonate and addition of these bases to the reaction mixture enables to perform many [2+2]cycloadditions with olefins, which, owing to acidity of the commercially available reagent, so far gave negative results.

    >