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  4. A Short and Convenient Synthesis of 1-Deoxymannojirimycin (DMJ) and N-oxy-Analogues from D-Fructose
 
research article

A Short and Convenient Synthesis of 1-Deoxymannojirimycin (DMJ) and N-oxy-Analogues from D-Fructose

Racine, Emilie
•
Bello, Claudia
•
Gerber-Lemaire, Sandrine  
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2009
The Journal of Organic Chemistry

The ketonitrone 8 was prepared from D-fructose as an inexpensive starting material, and was used in a stereoselective synthesis of 1-deoxymannojirimycin (4), its previously unknown N-hydroxy analogue 15, as well as the polyhydroxylated ketonitrone 14. The latter were assayed as potential glycosidase inhibitors on a panel of 13 selected purified enzymes. N-Hydroxy DMJ (15) exhibited a moderate and non selective activity towards the snail - mannosidase EC 3.2.1.25.

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Type
research article
DOI
10.1021/jo802255t
Web of Science ID

WOS:000263316600049

Author(s)
Racine, Emilie
Bello, Claudia
Gerber-Lemaire, Sandrine  
Vogel, Pierre  
Py, Sandrine
Date Issued

2009

Published in
The Journal of Organic Chemistry
Volume

74

Start page

1766

End page

1769

Subjects

1,3-Dipolar Cycloaddition Reactions

•

Lysosomal Storage Disorders

•

Natural-Product Sb-219383

•

Transfer-Rna Synthetase

•

Cyclic Nitrones

•

Glycosidase Inhibitors

•

Diastereoselective Synthesis

•

Absolute-Configuration

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Mannosidase Inhibitor

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Asymmetric-Synthesis

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LGSA  
Available on Infoscience
January 16, 2009
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/33808
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