JCGG ID |
JCGG-RAC0001516 | |||||||
Submitter |
The Noguchi Institute | |||||||
Reaction ID |
R-0000-001516 | |||||||
Regist Date |
2012/06/21 17:15:42 | |||||||
REACTANT | ||||||||
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Reactant Type |
glycal | |||||||
Mol |
0.44 mmol | |||||||
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Reactant Type |
alcohol | |||||||
Mol |
0.66 mmol | |||||||
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|||||||
Reactant Type |
NBS | |||||||
Mol |
0.53 mmol | |||||||
PRODUCT | ||||||||
MOLECULE ID |
|
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Yield |
88% | |||||||
REACTION DETAIL | ||||||||
Reaction Time |
0.5 hour, 1 hour | |||||||
Reaction Temp |
5 degree C, room temp | |||||||
Solvent |
MeCN/Et2O = 1/1, MeCN/Et2O = 1/1 | |||||||
Comment |
1) +all, 2) temperature change | |||||||
COMMENT | ||||||||
Keywords: The synthesis of 2-deoxy-glycoside, glycal donor | ||||||||
There are multiple steps in this reaction. | ||||||||
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-0000-000159 | |||||||
Source |
K. Tatsuta, K. Fujimoto, M. Kinoshita, and S. Umezawa, Carbohydr. Res., 54, 85 (1977) |
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST) |