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research article
Short, stereoselective syntheses of C(1 -> 3)-linked disaccharides
1998
Nucleophilic additions to D-isolevoglucosenone are face selective and generate the corresponding enolates which react with 1,2:3,4-di-O-isopropylidene-alpha-D-galacto-hexodialdo-1,5-pyranose to give aldol adducts. These can be reduced stereoselectively into C(1-->3) glycosides of 1,6-anhydro-D-galacto-pyranose. (C) 1997 Elsevier Science Ltd. All rights reserved.
Type
research article
Authors
Publication date
1998
Published in
Volume
39
Issue
1-2
Start page
31
End page
34
Subjects
Note
Univ Lausanne, Chim Sect, BCH, CH-1015 Lausanne, Switzerland.
Peer reviewed
REVIEWED
EPFL units
Available on Infoscience
November 9, 2005
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