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Glycan Syntheses |
JCGG ID |
JCGG-RAC0001639 | |||||||
Submitter |
The Noguchi Institute | |||||||
Reaction ID |
R-0000-001639
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Regist Date |
2012/06/21 17:30:20 | |||||||
| REACTANT | ||||||||
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Reactant Type |
AgOTf | |||||||
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Reactant Type |
SnCl2 | |||||||
| PRODUCT | ||||||||
MOLECULE ID |
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Yield |
21% | |||||||
| REACTION DETAIL | ||||||||
Reaction Time |
3 hours | |||||||
Reaction Temp |
room temp | |||||||
Solvent |
CHCl3/PhCH3 | |||||||
Comment |
Very few were described regarding this reaction. | |||||||
| COMMENT | ||||||||
| Keywords: synthesis of glycosphingolipid, Lewis X antigen, glycolipid | ||||||||
| 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-0000-000192 | |||||||
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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