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Glycan Syntheses |
JCGG ID |
JCGG-RAC0001825 | |||||||
Submitter |
The Noguchi Institute | |||||||
Reaction ID |
R-0000-001825
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Regist Date |
2012/06/21 18:06:36 | |||||||
| REACTANT | ||||||||
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Reactant Type |
mannopyranoside | |||||||
Mol |
13.8 mmol | |||||||
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Reactant Type |
AcOH (solvent) | |||||||
Volume |
38 mL | |||||||
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Reactant Type |
H2SO4 (3 M in H2O) | |||||||
Volume |
12 mL | |||||||
| PRODUCT | ||||||||
MOLECULE ID |
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Yield |
42% | |||||||
| REACTION DETAIL | ||||||||
Reaction Time |
4.5 hours | |||||||
Reaction Temp |
85 degree C | |||||||
Solvent |
AcOH | |||||||
| COMMENT | ||||||||
| Keywords: synthesis, cleavage, methyl 2,3,4,6-tetra-O-benzyl-alpha-D-mannopyranoside | ||||||||
| 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-0000-000256 | |||||||
Source |
Liebigs Ann. Chem. 1249 (1983) | |||||||
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST)
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