JCGG ID |
JCGG-RAC0001627 | |||||||
Submitter |
The Noguchi Institute | |||||||
Reaction ID |
R-0000-001627 | |||||||
Regist Date |
2012/06/21 17:28:18 | |||||||
REACTANT | ||||||||
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Mol |
34 micro mole | |||||||
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Reactant Type |
NaOMe (0.5 M in MeOH) | |||||||
Volume |
70 micro L | |||||||
PRODUCT | ||||||||
MOLECULE ID |
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Yield |
91% | |||||||
REACTION DETAIL | ||||||||
Reaction Time |
24 hours | |||||||
Reaction Temp |
60 degree C | |||||||
Solvent |
MeOH | |||||||
COMMENT | ||||||||
Keywords: synthesis of glycosphingolipid, globotriosylceramide, Gb3 | ||||||||
The reaction is the 2nd 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-0000-000191 | |||||||
Source |
K. C. Nicolaou, T. J. Caulfield, and H. Kataoka, Carbohydr. Res., 202, 177 (1990) |
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST) |