Synthesis 1987; 1987(8): 683-688
DOI: 10.1055/s-1987-28045
paper
© 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.

Sterically Crowded Sulfonate Esters: Novel Leaving Groups with Hindered S-O Cleavage

Thomas Netscher* , Horst Prinzbach
  • *Chemisches Laboratorium der Universität Freiburg i. Br., lnstitut für Organische Chemie und Biochemie, Albertstr. 21, D-7800 Freiburg, West Germany
Further Information

Publication History

Publication Date:
12 September 2002 (online)

Reagents and procedures for the preparation of tert-butyl sulfonate esters 2 and 2,2,2-trifluoro-1,1-diphenylethane sulfonate esters 3 (TDE-sulfonates) are described. In these new sulfonates, S-O-scission is reduced significantly by steric hindrance.

    >