JCGG ID |
JCGG-RAC0001537 | |||||||
Submitter |
The Noguchi Institute | |||||||
Reaction ID |
R-0000-001537 | |||||||
Regist Date |
2012/06/21 17:18:23 | |||||||
REACTANT | ||||||||
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Reactant Type |
TMSOTf | |||||||
PRODUCT | ||||||||
MOLECULE ID |
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Yield |
94% | |||||||
REACTION DETAIL | ||||||||
Reaction Time |
NOT specified | |||||||
Reaction Temp |
NOT specified | |||||||
Solvent |
CH2Cl2 | |||||||
Comment |
Very few were described regarding this reaction. | |||||||
COMMENT | ||||||||
The synthesis of 2-deoxy-glycoside, stereoselectivity control using C-2 substitution group | ||||||||
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-0000-000170 | |||||||
Source |
M. Trumtel, P. Tavecchiea, A. Veyrieres, and P. Sinay, Carbohydr. Res., 191, 29 (1989) |
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST) |