JCGGDB TOP Glycan Syntheses

Reaction

JCGG ID
JCGG-RAC0000187
Submitter
The Noguchi Institute
Reaction ID
R-0000-000187
Regist Date
2012/06/21 14:45:21
REACTANT
MOLECULE ID
JCGG-COM0000226 (Reaction Tree)
Reactant Type
1,3,4,6-tetra-O-benzyl-D-frucofuranosyl acetate(alpha/beta=1/2)
Mol
1
MOLECULE ID
JCGG-COM0000229
Reactant Type
Lewis acid(activator)
Mol
0.05
MOLECULE ID
JCGG-COM0000096
Mol
1
PRODUCT
MOLECULE ID
JCGG-COM0000227 (Reaction Tree)
Product Type
alpha
Yield
95%(alpha/beta=75/25)
MOLECULE ID
JCGG-COM0000228 (Reaction Tree)
Product Type
beta
Yield
95%(alpha/beta=75/25)
REACTION DETAIL
Reaction Time
0.5 to 2 hours
Reaction Temp
0 degree C
Solvent
PhCH3
Catalyst
activator
Cu(OTf)2
Comment
Anhydrous CaSO4 was included in the solvent.
COMMENT
The PMID could not be found.
REFERENCE
Reference Id
REF-0000-000011
Source
Tetrahedron Letters 48 (2007) 6458‐6462
Doi
10.1016/j.tetlet.2007.07.092

©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST)