JCGG ID |
JCGG-RAC0001733 | ||||
Submitter |
The Noguchi Institute | ||||
Reaction ID |
R-0000-001733 | ||||
Regist Date |
2012/06/21 17:47:20 | ||||
REACTANT | |||||
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Mol |
0.459 mmol | ||||
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Mol |
0.077 mmol | ||||
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Reactant Type |
AgOTf | ||||
Mol |
1.15 mmol | ||||
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Reactant Type |
Cp2HfCl2 | ||||
Mol |
1.15 mmol | ||||
PRODUCT | |||||
MOLECULE ID |
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Yield |
96% | ||||
REACTION DETAIL | |||||
Reaction Time |
4 hours, 1 hour | ||||
Reaction Temp |
below 5 degree C, room temp | ||||
Solvent |
CH2Cl2, CH2Cl2 | ||||
Comment |
1) +all, 2) temperature change | ||||
MS 4A was included in the solvent. | |||||
The reactants were mixed at 0 degree in Celsius before stirred at below 5 degree. (first step) | |||||
COMMENT | |||||
Keywords: glycosyl fluorides, glycosyl sulfides, trimeric Lex | |||||
There are multiple steps in this reaction. | |||||
REFERENCE | |||||
Reference Id |
REF-0000-000196 | ||||
Source |
PREPARATIVE CARBOHYDRATE CHEMISTRY | ||||
Reference Id |
REF-0000-000197 | ||||
Source |
ISBN 0-8247-9802-3 | ||||
Reference Id |
REF-0000-000227 | ||||
Source |
J. Am. Chem. Soc. 112:3693 (1990) |
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST) |