Synlett 2001; 2001(5): 0709-0711
DOI: 10.1055/s-2001-13385
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.

Scandium(III) Triflate/Isopropyl-Pybox Complex as an Efficient Catalyst for Asymmetric Diels-Alder Reaction

Shin-ichi Fukuzawa* , Hiroshi Matsuzawa, Ken Metoki
  • *Department of Applied Chemistry, Institute of Science and Engineering, Chuo University, Kasuga, Bunkyo-ku, Tokyo 112-8551, Japan; Fax 81-(0)3-3817-1895; E-mail: fukuzawa@chem.chuo-u.ac.jp
Further Information

Publication History

Publication Date:
31 December 2001 (online)

The chiral scandium(III) triflate/i-Pr-pybox complex efficiently catalyzes the asymmetric Diels-Alder reaction of 1,3-dienes with acyl-1,3-oxazolidin-2-ones (1 a - c) afford the corresponding adducts in good yields with up to 90% ee. The reaction can be carried out in less toxic benzotrifluoride and supercritical carbon dioxide while remaining good selectivity (65-75% ee).

    >