Synlett 1995; 1995(12): 1255-1256
DOI: 10.1055/s-1995-5258
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.

Asymmetric Synthesis of (S)-Chromanethanol as a Useful Synthetic Unit of Vitamin E Analogs

Eisaku Mizuguchi, Kazuo Achiwa*
  • *School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Shizuoka 422, JAPAN
Further Information

Publication History

Publication Date:
31 December 2000 (online)

The Optically active chromanethanol(1) was synthesized by utilizing the catalytic asymmetric Sharpless epoxidation as a key reaction. Cyclization of the diol(7) to the (S)-O-benzyl chromanethanol(8) with Ph3CBF4 in one step was observed to proceed with complete retention of the configuration.

    >