JCGG ID |
JCGG-RAC0001491 | |||||||
Submitter |
The Noguchi Institute | |||||||
Reaction ID |
R-0000-001491 | |||||||
Regist Date |
2012/06/21 17:11:32 | |||||||
REACTANT | ||||||||
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PRODUCT | ||||||||
MOLECULE ID |
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Yield |
80% | |||||||
REACTION DETAIL | ||||||||
Reaction Time |
30 minutes | |||||||
Reaction Temp |
140 degree C | |||||||
Solvent |
NOT specified | |||||||
Comment |
Very few were described regarding this reaction. | |||||||
COMMENT | ||||||||
Keywords: The synthesis of 1,2-trans-glycoside, alpha-mannopyranoside | ||||||||
This reaction employed a unique method called thermal glycosidation. (generally poor selectivity except alpha-mannoglycosidation) | ||||||||
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-0000-000138 | |||||||
Source |
M. Nishizawa, Y. Kan, W. Shimomoto, and H. Yamada, Tetrahedron Lett., 31, 2431 (1990) |
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST) |