|
Glycan Syntheses |
JCGG ID |
JCGG-RAC0001727 | |||||||
Submitter |
The Noguchi Institute | |||||||
Reaction ID |
R-0000-001727
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Regist Date |
2012/06/21 17:44:58 | |||||||
| REACTANT | ||||||||
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|
|
|
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Mol |
0.69 mmol | |||||||
|
|
|
|||||||
Mol |
0.68 mmol | |||||||
| PRODUCT | ||||||||
MOLECULE ID |
|
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Yield |
86% | |||||||
| REACTION DETAIL | ||||||||
Reaction Time |
1 hour | |||||||
Reaction Temp |
room temp | |||||||
Solvent |
dry CH2Cl2 | |||||||
| COMMENT | ||||||||
| Keywords: glycosylation, O-glycosyl trichloroacetimidates | ||||||||
| REFERENCE | ||||||||
Reference Id |
REF-0000-000196 | |||||||
Source |
PREPARATIVE CARBOHYDRATE CHEMISTRY | |||||||
Reference Id |
REF-0000-000197 | |||||||
Source |
ISBN 0-8247-9802-3 | |||||||
Reference Id |
REF-0000-000224 | |||||||
Source |
Liebigs Ann. Chem. p. 121 (1991) | |||||||
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST)
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