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Glycan Syntheses |
JCGG ID |
JCGG-RAC0000359 | |||||||
Submitter |
The Noguchi Institute | |||||||
Reaction ID |
R-0000-000359
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Regist Date |
2012/06/21 15:40:24 | |||||||
| REACTANT | ||||||||
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Reactant Type |
Donor | |||||||
Mol |
1 equiv. | |||||||
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Reactant Type |
Alcohol | |||||||
Mol |
1 equiv. | |||||||
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Reactant Type |
activator | |||||||
Mol |
1 equiv. | |||||||
| PRODUCT | ||||||||
MOLECULE ID |
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Product Type |
alpha | |||||||
Yield |
75% | |||||||
| REACTION DETAIL | ||||||||
Reaction Time |
overnight | |||||||
Reaction Temp |
room temp | |||||||
Solvent |
PhH | |||||||
Catalyst |
activator | |||||||
Comment |
MS 4A was included in the solvent. | |||||||
| The reaction was sheltered from the light. | ||||||||
| COMMENT | ||||||||
| The PMID could not be found. | ||||||||
| Only alpha was detected in the product. | ||||||||
| The alpha/beta ratio was determined by 13C NMR spectroscopy. | ||||||||
| REFERENCE | ||||||||
Reference Id |
REF-0000-000014 | |||||||
Source |
Bulletin of the Chemical Society of Japan, Vol. 67 (1994), No. 5 pp.1359-1366 | |||||||
Doi |
10.1246/bcsj.67.1359 | |||||||
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST)
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