Download PDF
Synlett 1996; 1996(10): 971-972
DOI: 10.1055/s-1996-5652
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.

Non-Carbohydrate Route to Levoglucosenone and Its Enantiomer Employing Asymmetric Dihydroxylation

Takahiko Taniguchi, Keiichi Nakamura, Kunio Ogasawara*
  • *Pharmaceutical Institute, Tohoku University, Aobayama, Sendai 980-77, Japan, Fax +81-22-217-6845; E-mail c21799@cctu.cc.tohoku.ac.jp
Further Information

Publication History

Publication Date:
31 December 2000 (online)

 PDF Download  Permissions and Reprints All articles of this category

Levoglucosenone and its enantiomer have been prepared in an enantiocontrolled manner from a non-carbohydrate prochiral precursor 2-vinylfuran via the corresponding isolevoglucosenone precursors employing the Sharpless asymmetric dihydroxylation (AD reaction) as key step.

chiral building block - levoglucosenone - ent-levoglucosenone - asymmetric dihydroxylation - isolevoglucosenone