A Total, Asymmetric-Synthesis of 2-Deoxy-L-Fucose from Furan
1992
Abstract
The Diels-Alder adduct (+)-l of furan to 1-cyanovinyl (1'S)-camphanate was converted to methyl 3,5-O-diacetyl-2,6-dideoxy-beta-L-lyxo-hexofurano-side ((+)-12), a protected form of 2-deoxy-L-fucose, in 8 steps and 16.6% overall yield.
Details
Title
A Total, Asymmetric-Synthesis of 2-Deoxy-L-Fucose from Furan
Author(s)
Durgnat, J. M. ; Warm, A. ; Vogel, P.
Published in
Synthetic Communications
Volume
22
Issue
13
Pages
1883-1893
Date
1992
ISSN
0039-7911
Keywords
Note
Univ lausanne,chim sect,2 rue barre,ch-1005 lausanne,switzerland.
Laboratories
LGSA
Record Appears in
Scientific production and competences > SB - School of Basic Sciences > SB Archives > LGSA - Laboratory of Glycochemistry and Asymmetric Synthesis
Peer-reviewed publications
Work produced at EPFL
Journal Articles
Published
Peer-reviewed publications
Work produced at EPFL
Journal Articles
Published
Record creation date
2005-11-09