JCGG ID |
JCGG-RAC0001715 | ||||
Submitter |
The Noguchi Institute | ||||
Reaction ID |
R-0000-001715 | ||||
Regist Date |
2012/06/21 17:42:54 | ||||
REACTANT | |||||
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Mol |
0.369 mmol | ||||
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Reactant Type |
Pd/C (10%) | ||||
Weight |
390 mg | ||||
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Reactant Type |
H2 (gas) | ||||
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Reactant Type |
pyridine (solvent) | ||||
Volume |
5 mL | ||||
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Reactant Type |
Ac2O (solvent) | ||||
Volume |
1 mL | ||||
PRODUCT | |||||
MOLECULE ID |
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Product Type |
alpha | ||||
Yield |
91%(alpha/beta=32/1) | ||||
MOLECULE ID |
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Product Type |
beta | ||||
Yield |
91%(alpha/beta=32/1) | ||||
REACTION DETAIL | |||||
Reaction Time |
4 hours, 15 hours | ||||
Reaction Temp |
NOT specified, room temp | ||||
Solvent |
dioxane, pyridine/Ac2O = 5/1 | ||||
Comment |
1) 36+Pd/C, H2, 2) +all the rest | ||||
COMMENT | |||||
Keywords: glycosylation, O-glycosyl trichloroacetimidates | |||||
The reaction is the 2nd part of the sequence. | |||||
There are multiple steps in this reaction. | |||||
REFERENCE | |||||
Reference Id |
REF-0000-000196 | ||||
Source |
PREPARATIVE CARBOHYDRATE CHEMISTRY | ||||
Reference Id |
REF-0000-000197 | ||||
Source |
ISBN 0-8247-9802-3 | ||||
Reference Id |
REF-0000-000215 | ||||
Source |
Liebigs Ann. Chem. p. 543 (1993) |
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST) |