JCGG ID |
JCGG-RAC0001813 | |||||||
Submitter |
The Noguchi Institute | |||||||
Reaction ID |
R-0000-001813 | |||||||
Regist Date |
2012/06/21 18:02:46 | |||||||
REACTANT | ||||||||
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|
|
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Mol |
2.6 mmol | |||||||
|
|
|||||||
Mol |
5.2 mmol | |||||||
|
|
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Reactant Type |
DMTST | |||||||
Mol |
3.0 equiv. (relative to the donor) | |||||||
PRODUCT | ||||||||
MOLECULE ID |
|
|
|
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Product Type |
alpha | |||||||
Yield |
70% | |||||||
REACTION DETAIL | ||||||||
Reaction Time |
17 hours | |||||||
Reaction Temp |
-15 degree C | |||||||
Solvent |
dry MeCN | |||||||
Comment |
16, 11, and MS 3A were mixed and stirred for 6 hours at room temperature before the reaction. | |||||||
MS 3A was included in the solvent. | ||||||||
The reactants were mixed at -30 degree in Celsius before stirred at -15 degree. | ||||||||
COMMENT | ||||||||
Keywords: synthesis, sialyl glycosides, sialylation, 3-O-benzoyl-galactose | ||||||||
REFERENCE | ||||||||
Reference Id |
REF-0000-000196 | |||||||
Source |
PREPARATIVE CARBOHYDRATE CHEMISTRY | |||||||
Reference Id |
REF-0000-000197 | |||||||
Source |
ISBN 0-8247-9802-3 | |||||||
Reference Id |
REF-0000-000242 | |||||||
Source |
Carbohydr. Res. 184:C1 (1988) | |||||||
Reference Id |
REF-0000-000243 | |||||||
Source |
Carbohydr. Res. 212:277 (1991) |
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST) |