|
Glycan Syntheses |
JCGG ID |
JCGG-RAC0001725 | |||||||
Submitter |
The Noguchi Institute | |||||||
Reaction ID |
R-0000-001725
|
|||||||
Regist Date |
2012/06/21 17:44:50 | |||||||
| REACTANT | ||||||||
|
|
|
|
||||||
Mol |
1.0 mmol | |||||||
|
|
|
|||||||
Reactant Type |
HCl | |||||||
Mol |
saturated | |||||||
| PRODUCT | ||||||||
MOLECULE ID |
|
|
|
|||||
Yield |
78% | |||||||
| REACTION DETAIL | ||||||||
Reaction Time |
4 hours | |||||||
Reaction Temp |
room temp | |||||||
Solvent |
dry CH2Cl2 | |||||||
| COMMENT | ||||||||
| Keywords: glycosylation, O-glycosyl trichloroacetimidates | ||||||||
| 5% of alpha-halogenose was also obtained. | ||||||||
| REFERENCE | ||||||||
Reference Id |
REF-0000-000196 | |||||||
Source |
PREPARATIVE CARBOHYDRATE CHEMISTRY | |||||||
Reference Id |
REF-0000-000197 | |||||||
Source |
ISBN 0-8247-9802-3 | |||||||
Reference Id |
REF-0000-000223 | |||||||
Source |
Liebigs Ann. Chem. p. 680 (1984) | |||||||
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST)
|
