Download PDF
Synlett 1995; 1995(4): 363-364
DOI: 10.1055/s-1995-4963
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 2-Substituted Pyrrolines by an Intramolecular Schmidt Reaction of 4-Substituted 3-Butenyl Azides

Pedro Molina* , Julián Alcántara, Carmen López-Leonardo
  • *Departamento de Química Orgánica, Facultad de Química, Universidad de Murcia, Campus de Espinardo, E-30071, Murcia, Spain
Further Information

Publication History

Publication Date:
31 December 2000 (online)

  PDF Download  Permissions and Reprints All articles of this category

4-Substituted 3-butenyl azides readily undergo an intramolecular carbocation version of the Schmidt reaction with trifluoromethanesulfonic acid at 0 °C to give 2-substituted pyrrolines.

Intramolecular Schmidt reaction - 3-Butenyl azides - 2-Substituted pyrrolines

      >