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Glycan Syntheses |
JCGG ID |
JCGG-RAC0001882 | ||||
Submitter |
The Noguchi Institute | ||||
Reaction ID |
R-0000-001882
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Regist Date |
2012/06/21 18:11:36 | ||||
| REACTANT | |||||
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Reactant Type |
NaOMe | ||||
| PRODUCT | |||||
MOLECULE ID |
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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, N-protection, amino sugars, N-tetrachlorophthalimido, TCP | |||||
| The reaction is the 1st 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-0000-000285 | ||||
Source |
Liebigs Ann. Chem. 791 (1997) | ||||
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST)
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