JCGG ID |
JCGG-RAC0001701 | |||||||
Submitter |
The Noguchi Institute | |||||||
Reaction ID |
R-0000-001701 | |||||||
Regist Date |
2012/06/21 17:39:11 | |||||||
REACTANT | ||||||||
|
|
|||||||
Mol |
22.2 mmol | |||||||
|
|
|||||||
Reactant Type |
CCl3CN | |||||||
Mol |
99 mmol | |||||||
|
|
|||||||
Reactant Type |
NaH | |||||||
Mol |
2.08 + 29.2 mmol | |||||||
PRODUCT | ||||||||
MOLECULE ID |
|
|
|
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Yield |
96% | |||||||
REACTION DETAIL | ||||||||
Reaction Time |
15 minutes + 2 hours | |||||||
Reaction Temp |
room temp | |||||||
Solvent |
dry CH2Cl2 | |||||||
Comment |
The second addition of NaH was performed 15 minutes after the start of the reaction. | |||||||
COMMENT | ||||||||
Keywords: synthesis, O-glycosyl trichloroacetimidates | ||||||||
REFERENCE | ||||||||
Reference Id |
REF-0000-000196 | |||||||
Source |
PREPARATIVE CARBOHYDRATE CHEMISTRY | |||||||
Reference Id |
REF-0000-000197 | |||||||
Source |
ISBN 0-8247-9802-3 | |||||||
Reference Id |
REF-0000-000204 | |||||||
Source |
Liebigs Ann. Chem. p. 1249 (1983) |
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST) |