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  4. Synthesis of α-(1→3)- and α-(1→4)-linked c-disaccharides using (+)-7-oxabicyclo[2.2.1]hept-5-en-2-one (“naked sugar”)
 
research article

Synthesis of α-(1→3)- and α-(1→4)-linked c-disaccharides using (+)-7-oxabicyclo[2.2.1]hept-5-en-2-one (“naked sugar”)

Bimwala, R. M.
•
Vogel, P.  
1991
Tetrahedron Letters

The alpha-(1-->3)- and alpha-(1-->4)-linked C-disaccharides derived from D-glucose and L-mannose have been obtained with high stereoselectivity via the addition of 2,3,4,6-tetra-O-acetyl-glucopyranosyl radical to (1S,4R,5R,6R)-6-endo-chloro-3-methylidene-5-benzeneselenyl-7-oxabicyclo[ 2.2.1]heptan-2-one.

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Type
research article
DOI
10.1016/0040-4039(91)80349-B
Author(s)
Bimwala, R. M.
Vogel, P.  
Date Issued

1991

Publisher

Elsevier

Published in
Tetrahedron Letters
Volume

32

Issue

11

Start page

1429

End page

1432

Subjects

Electrophilic additions

•

vinyl carbanions

•

carbonyl group

•

derivatives

•

substituent

•

inhibitors

•

sucrose

Note

Univ lausanne,chim sect,2 rue la 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/20.500.14299/219642
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