JCGG ID |
JCGG-RAC0001923 | |||||||
Submitter |
The Noguchi Institute | |||||||
Reaction ID |
R-0000-001923 | |||||||
Regist Date |
2012/06/21 18:14:59 | |||||||
REACTANT | ||||||||
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Mol |
33.5 mmol | |||||||
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Reactant Type |
DBU | |||||||
Mol |
3.40 mmol | |||||||
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|||||||
Reactant Type |
Cl3CCN | |||||||
Mol |
unknown | |||||||
PRODUCT | ||||||||
MOLECULE ID |
|
|
|
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Yield |
97% | |||||||
REACTION DETAIL | ||||||||
Reaction Time |
2 hours, 10 hours | |||||||
Reaction Temp |
0 degree C, room temp | |||||||
Solvent |
dry CH2Cl2, dry CH2Cl2 | |||||||
Comment |
1) +all, 2) temperature change | |||||||
COMMENT | ||||||||
Keywords: synthesis, trichloroacetimidate method, DBU | ||||||||
ATTENTION: Cl3CCN appearing in the scheme is not mentioned in the written method. | ||||||||
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 | |||||||
Reference Id |
REF-0000-000292 | |||||||
Source |
Org. Biomol. Chem. 4, 3901 (2006) | |||||||
Reference Id |
REF-0000-000293 | |||||||
Source |
Tetrahedron Asym. 9, 781 (1998) |
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST) |