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  4. A Total, Asymmetric-Synthesis of 2-Deoxy-L-Fucose from Furan
 
research article

A Total, Asymmetric-Synthesis of 2-Deoxy-L-Fucose from Furan

Durgnat, J. M.
•
Warm, A.
•
Vogel, P.  
1992
Synthetic Communications

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
  • Metrics
Type
research article
DOI
10.1080/00397919208021319
Author(s)
Durgnat, J. M.
Warm, A.
Vogel, P.  
Date Issued

1992

Published in
Synthetic Communications
Volume

22

Issue

13

Start page

1883

End page

1893

Subjects

Pure 7-oxabicyclo<2.2.1>hept-5-en-2-yl derivatives

•

naked sugars

•

antitumor antibiotics

•

digitoxose

•

efficient

Note

Univ lausanne,chim sect,2 rue barre,ch-1005 lausanne,switzerland.

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LGSA  
Available on Infoscience
November 9, 2005
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/219663
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