Synlett 1996; 1996(9): 856-858
DOI: 10.1055/s-1996-5600
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.

Glycals as Ambident Electrophiles Towards Organometallic Nucleophiles. Stereoselective Synthesis of C(3)-Branched Carbohydrates

Simon N. Thorn, Timothy Gallagher*
  • *School of Chemistry, University of Bristol, Bristol BS8 1TS, U.K.
Further Information

Publication History

Publication Date:
31 December 2000 (online)

Reaction of glycals with simple and functionalised alkyl Zn/Cu reagents in the presence of BF3.OEt2 leads to C(3)-branched carbohydrates with complete control of stereochemistry at C(3).