JCGG ID |
JCGG-RAC0001626 | |||||||
Submitter |
The Noguchi Institute | |||||||
Reaction ID |
R-0000-001626 | |||||||
Regist Date |
2012/06/21 17:28:13 | |||||||
REACTANT | ||||||||
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|
|
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Mol |
40 micro mole | |||||||
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|
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Reactant Type |
TBAF (1.1 M in THF) | |||||||
Volume |
44 micro L | |||||||
PRODUCT | ||||||||
MOLECULE ID |
|
|
|
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Yield |
95% | |||||||
REACTION DETAIL | ||||||||
Reaction Time |
2 hours | |||||||
Reaction Temp |
NOT specified | |||||||
Solvent |
THF | |||||||
COMMENT | ||||||||
Keywords: synthesis of glycosphingolipid, globotriosylceramide, Gb3 | ||||||||
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-0000-000191 | |||||||
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) |