Synlett 1991; 1991(4): 238-240
DOI: 10.1055/s-1991-20691
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.

New Synthetic Method for Allylic Isocyanates Through [3,3] Sigmatropic Rearrangement of Allylic Cyanates

Yoshiyasu Ichikawa*
  • *Faculty of Education, Mie University, Tsu, Mie 514, Japan
Further Information

Publication History

Publication Date:
07 March 2002 (online)

Dehydration of allylic carbamates has been proved to be an effective method for the synthesis of allylic cyanates, which immediately rearrange to allylic isocyanates at or below ambient temperature. The allylic isocyanates (6 examples) were characterized by further reaction with pyrrolidine to provide stable and easily isolable ureas. This process offers a useful synthetic tool for the construction of the allylic amine moiety from allylic alcohols. The efficiency, scope and limitations of this new method were examined.

    >