Synlett 2000; 2000(6): 0877-0879
DOI: 10.1055/s-2000-6705
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.

Catalysis by Lithium Cation: Lithium Trifluoromethanesulfonate as a Substitute for Lithium Perchlorate in Cycloadditions

Jacques Augé* , Richard Gil, Sophie Kalsey, Nadège Lubin-Germain
  • *Unité associée au CNRS, FRE 2126, Université de Cergy-Pontoise, 5 mail Gay-Lussac, Neuville-sur-Oise, 95031 Cergy-Pontoise, France; Fax 33 1 34257071; E-mail: Jacques.Auge@chim.u-cergy.fr
Further Information

Publication History

Publication Date:
31 December 2000 (online)

Lithium trifluoromethanesulfonate, an easily accessible lithium salt, is shown to be a safe alternative to lithium perchlorate as a promotor in organic Diels-Alder and hetero Diels-Alder reactions.

    >