JCGG ID |
JCGG-RAC0001988 | ||||
Submitter |
The Noguchi Institute | ||||
Reaction ID |
R-0000-001988 | ||||
Regist Date |
2012/06/21 18:21:27 | ||||
REACTANT | |||||
|
|
||||
Reactant Type |
sugar | ||||
|
|
||||
Reactant Type |
TBAF | ||||
|
|
||||
Reactant Type |
CCl3CN | ||||
|
|
||||
Reactant Type |
DBU | ||||
PRODUCT | |||||
MOLECULE ID |
|
|
|||
Yield |
NOT specified | ||||
REACTION DETAIL | |||||
Reaction Time |
NOT specified, NOT specified | ||||
Reaction Temp |
NOT specified, NOT specified | ||||
Solvent |
THF, NOT specified | ||||
Comment |
1) sugar+TBAF, 2) +CCl3CN, DBU | ||||
Very few were described regarding this reaction. | |||||
COMMENT | |||||
Keywords: synthesis, glycosylation strategies, block synthesis, tetrameric LewisX | |||||
The reaction is the 4th part of the sequence. | |||||
There are multiple steps in this reaction. | |||||
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) |