Download PDF
Synlett 2001; 2001(2): 0232-0233
DOI: 10.1055/s-2001-10783
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.

Preparation of N-Sulfonylimines Bearing Easily Removable Protecting Groups via the Hudson Reaction of Oximes with Sulfinyl Chlorides

Gerald D. Artman III* , Alessandra Bartolozzi, Richard W. Franck, Steven M. Weinreb
  • *Department of Chemistry, The Pennsylvania State University, University Park, Pennsylvania 16802, USA; Fax 814-863-8403; E-mail: smw§chem.psu.edu
Further Information

Publication History

Publication Date:
31 December 2001 (online)

  PDF Download  Permissions and Reprints All articles of this category

N-Sulfonylimines which incorporate easily cleavable t-butylsulfonyl (Bus) and β-trimethylsilylethanesulfonyl (SES) groups on nitrogen can be readily synthesized from oximes and the corresponding sulfinyl chloride by the Hudson reaction.

imines - sulfonamides - radical reactions