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  4. Synthesis of a new C(1 -> 2)-linked iminodisaccharide starting from levoglucosenone
 
research article

Synthesis of a new C(1 -> 2)-linked iminodisaccharide starting from levoglucosenone

Navarro, I.
•
Vogel, P.  
2002
Helvetica Chimica Acta

Methyl 2-deoxy-2-[(1S)-2.5-dideoxy-2.5-imino-L-ribitol-1-C-yl)-alpha-D-glucopyr anoside ((+)-6) was obtained from the product of Nozaki-Kishi coupling of 2,5-{[(tert-butoxy)carbonyl]imino}-2,5-dideoxy-3,4-O-isopropl-idene-L-ri bose ((-)-9) and 4-0-benzyl-6-O-[(benzyloxy)methyl]-3-deoxy-2-O-[(trifluoromethyl)sulfony l]-alpha-D-erythro-hex-2-enopyranosicle ((+)-12). The alkenyl triflato (+)-12 was derived from levoglucosenone (1).

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Type
research article
DOI
10.1002/1522-2675(200201)85:1<152::AID-HLCA152>3.0.CO;2-L
Web of Science ID

WOS:000173955600011

Author(s)
Navarro, I.
Vogel, P.  
Date Issued

2002

Published in
Helvetica Chimica Acta
Volume

85

Issue

1

Start page

152

End page

160

Subjects

Aza-c-disaccharides

•

immunodeficiency virus type-1

•

conformational

•

differences

•

imino disaccharides

•

oligosaccharide mimetics

•

n-butyldeoxynojirimycin

•

glycosidase inhibitors

•

envelope

•

glycoproteins

•

biological evaluation

•

convergent synthesis

Note

Ecole Polytech Fed Lausanne, Inst Chim Organ, BCH, CH-1015 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/20.500.14299/219801
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