JCGG ID |
JCGG-RAC0001925 | |||||||
Submitter |
The Noguchi Institute | |||||||
Reaction ID |
R-0000-001925 | |||||||
Regist Date |
2012/06/21 18:15:06 | |||||||
REACTANT | ||||||||
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|
|
||||||
Reactant Type |
donor | |||||||
Mol |
4.42 mmol | |||||||
|
|
|||||||
Reactant Type |
acceptor | |||||||
Mol |
2.21 mmol | |||||||
|
|
|||||||
Reactant Type |
TMSOTf (in 1.5 mL of Et2O) | |||||||
Mol |
50 micromole | |||||||
PRODUCT | ||||||||
MOLECULE ID |
|
|
||||||
Yield |
75% | |||||||
REACTION DETAIL | ||||||||
Reaction Time |
more than 5 hours | |||||||
Reaction Temp |
-20 degree C | |||||||
Solvent |
dry Et2O | |||||||
Comment |
TMSOTf was added dropwise. | |||||||
COMMENT | ||||||||
Keywords: synthesis, trichloroacetimidate method, TMSOTf | ||||||||
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-0000-000295 | |||||||
Source |
Liebigs Ann. Chem. 1826 (1984) |
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST) |