|
Glycan Syntheses |
JCGG ID |
JCGG-RAC0001459 | ||||
Submitter |
The Noguchi Institute | ||||
Reaction ID |
R-0000-001459
|
||||
Regist Date |
2012/06/21 17:06:30 | ||||
| REACTANT | |||||
|
|
|
||||
|
|
|
||||
|
|
|
||||
Reactant Type |
AgOSO2CF3 | ||||
| PRODUCT | |||||
MOLECULE ID |
|
|
|||
Yield |
82% | ||||
| REACTION DETAIL | |||||
Reaction Time |
NOT specified | ||||
Reaction Temp |
-30 degree C | ||||
Solvent |
CH2Cl2 | ||||
Comment |
Very few were described regarding this reaction. | ||||
| COMMENT | |||||
| Keywords: The synthesis of 1,2-cis-glycoside, beta-mannopyranoside | |||||
| The reaction is the 1st part of the sequence. | |||||
| REFERENCE | |||||
Reference Id |
REF-0000-000073 | ||||
Source |
第4版 実験化学講座 (26), 丸善 | ||||
Reference Id |
REF-0000-000074 | ||||
Source |
ISBN 4-621-03702-1 | ||||
Reference Id |
REF-0000-000113 | ||||
Source |
H. Kunz and W. Gunther, Angew. Chem., Int. Ed. Engl., 27, 1086 (1988) | ||||
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST)
|