JCGG ID |
JCGG-RAC0000453 | ||||
Submitter |
The Noguchi Institute | ||||
Reaction ID |
R-0000-000454 | ||||
Regist Date |
2012/06/21 16:07:28 | ||||
REACTANT | |||||
|
|
||||
Reactant Type |
Substrate | ||||
Mol |
1 equiv. | ||||
|
|
||||
Reactant Type |
Nucleophile | ||||
Mol |
3 equiv. | ||||
|
|
||||
Reactant Type |
cat. | ||||
Mol |
0.2 equiv. | ||||
PRODUCT | |||||
MOLECULE ID |
|
|
|||
Yield |
94% | ||||
REACTION DETAIL | |||||
Reaction Time |
2 to 3 hours | ||||
Reaction Temp |
-78 degree C | ||||
Solvent |
MeCN-CH2Cl2(1:1) | ||||
Catalyst |
cat. | ||||
Comment |
CaSO4 was added to the solvent as a drying agent. | ||||
COMMENT | |||||
The PMID could not be found. | |||||
The anomer ratio was NOT specified. | |||||
REFERENCE | |||||
Reference Id |
REF-0000-000018 | ||||
Source |
SYNTHESIS 2007, No. 19, pp 3021-3031 | ||||
Doi |
10.1055/s-2007-983882 |
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST) |