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Glycan Syntheses |
JCGG ID |
JCGG-RAC0002000 | ||||
Submitter |
The Noguchi Institute | ||||
Reaction ID |
R-0000-002000
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Regist Date |
2012/06/21 18:23:49 | ||||
| REACTANT | |||||
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Reactant Type |
NaOMe | ||||
| PRODUCT | |||||
MOLECULE ID |
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Product Type |
intermediate | ||||
Yield |
NOT specified | ||||
| REACTION DETAIL | |||||
Reaction Time |
NOT specified | ||||
Reaction Temp |
NOT specified | ||||
Solvent |
MeOH | ||||
Comment |
Very few were described regarding this reaction. | ||||
| COMMENT | |||||
| Keywords: synthesis, glycosylation strategies, thioglycoside donor, armed-disarmed concept | |||||
| The reaction is the 2nd part of the sequence. | |||||
| REFERENCE | |||||
Reference Id |
REF-0000-000253 | ||||
Source |
Essentials of Carbohydrate Chemistry and Biochemistry | ||||
Reference Id |
REF-0000-000254 | ||||
Source |
ISBN 978-3-527-31528-4 | ||||
Reference Id |
REF-0000-000312 | ||||
Source |
Org. Lett. 3, 4201 (2001) | ||||
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST)
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