|
Glycan Syntheses |
JCGG ID |
JCGG-RAC0001992 | ||||
Submitter |
The Noguchi Institute | ||||
Reaction ID |
R-0000-001992
|
||||
Regist Date |
2012/06/21 18:22:35 | ||||
| REACTANT | |||||
|
|
|
||||
Reactant Type |
Armed | ||||
|
|
|
||||
Reactant Type |
Disarmed | ||||
|
|
|
||||
Reactant Type |
IDCP | ||||
| PRODUCT | |||||
MOLECULE ID |
|
|
|||
Yield |
63% | ||||
| REACTION DETAIL | |||||
Reaction Time |
10 hours | ||||
Reaction Temp |
NOT specified | ||||
Solvent |
Et2O/CH2Cl2 | ||||
Comment |
Very few were described regarding this reaction. | ||||
| COMMENT | |||||
| Keywords: synthesis, glycosylation strategies, armed-disarmed principle | |||||
| 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 | ||||
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST)
|