|
Glycan Syntheses |
JCGG ID |
JCGG-RAC0001802 | |||||||
Submitter |
The Noguchi Institute | |||||||
Reaction ID |
R-0000-001802
|
|||||||
Regist Date |
2012/06/21 17:58:59 | |||||||
| REACTANT | ||||||||
|
|
|
|||||||
|
|
|
|
||||||
|
|
|
|||||||
Reactant Type |
NIS | |||||||
|
|
|
|||||||
Reactant Type |
TfOH | |||||||
| PRODUCT | ||||||||
MOLECULE ID |
|
|
||||||
Yield |
86% | |||||||
| REACTION DETAIL | ||||||||
Reaction Time |
NOT specified | |||||||
Reaction Temp |
-60 degree C | |||||||
Solvent |
CH2Cl2 | |||||||
Comment |
Very few were described regarding this reaction. | |||||||
| COMMENT | ||||||||
| Keywords: synthesis, sialyl glycosides, systematic synthesis, gangliosides, sialyloligosaccharides, sialyl galactose | ||||||||
| The reaction is the 3rd part of the sequence. | ||||||||
| REFERENCE | ||||||||
Reference Id |
REF-0000-000196 | |||||||
Source |
PREPARATIVE CARBOHYDRATE CHEMISTRY | |||||||
Reference Id |
REF-0000-000197 | |||||||
Source |
ISBN 0-8247-9802-3 | |||||||
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST)
|
