JCGG ID |
JCGG-RAC0001984 | ||||
Submitter |
The Noguchi Institute | ||||
Reaction ID |
R-0000-001984 | ||||
Regist Date |
2012/06/21 18:20:54 | ||||
REACTANT | |||||
|
|
||||
Reactant Type |
trichloroacetimidate | ||||
Mol |
4.0 mmol | ||||
|
|
||||
Reactant Type |
acceptor | ||||
Mol |
4.5 mmol | ||||
|
|
||||
Reactant Type |
TMSOTf | ||||
Mol |
40 micro mole | ||||
|
|
||||
Reactant Type |
NaHCO3 (solid) | ||||
Weight |
0.5 g | ||||
PRODUCT | |||||
MOLECULE ID |
|
|
|||
Yield |
80% | ||||
REACTION DETAIL | |||||
Reaction Time |
10 minutes | ||||
Reaction Temp |
-40 degree C | ||||
Solvent |
dry MeCN | ||||
COMMENT | |||||
Keywords: synthesis, glycosylation strategies, block synthesis, LewisX dimer intermediate | |||||
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 | ||||
Reference Id |
REF-0000-000310 | ||||
Source |
Tetrahedron Lett. 38, 1173 (1997) |
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST) |