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Glycan Syntheses |
JCGG ID |
JCGG-RAC0001631 | ||||
Submitter |
The Noguchi Institute | ||||
Reaction ID |
R-0000-001631
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Regist Date |
2012/06/21 17:28:52 | ||||
| REACTANT | |||||
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Reactant Type |
CCl3CN | ||||
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Reactant Type |
DBU | ||||
| PRODUCT | |||||
MOLECULE ID |
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Yield |
67% | ||||
| REACTION DETAIL | |||||
Reaction Time |
1 hour | ||||
Reaction Temp |
20 degree C | ||||
Solvent |
ClCCH2CH2l | ||||
Comment |
Very few were described regarding this reaction. | ||||
| COMMENT | |||||
| Keywords: synthesis of glycosphingolipid, Lewis X antigen, glycolipid | |||||
| 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-0000-000192 | ||||
Source |
S. Sato, Y. Ito, T. Nukada, Y. Nakahara, and T. Ogawa, Carbohydr. Res., 167, 197 (1987) | ||||
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST)
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