JCGG ID |
JCGG-RAC0001620 | ||||
Submitter |
The Noguchi Institute | ||||
Reaction ID |
R-0000-001620 | ||||
Regist Date |
2012/06/21 17:26:54 | ||||
REACTANT | |||||
|
|
||||
|
|
||||
Reactant Type |
NBS | ||||
|
|
||||
Reactant Type |
HF | ||||
|
|
||||
Reactant Type |
pyridine | ||||
PRODUCT | |||||
MOLECULE ID |
|
|
|||
Yield |
89% | ||||
REACTION DETAIL | |||||
Reaction Time |
NOT specified | ||||
Reaction Temp |
-35 to 0 degree C | ||||
Solvent |
CH2Cl2 | ||||
Comment |
Very few were described regarding this reaction. | ||||
COMMENT | |||||
Keywords: synthesis of glycosphingolipid, globotriosylceramide, Gb3 | |||||
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-0000-000191 | ||||
Source |
K. C. Nicolaou, T. J. Caulfield, and H. Kataoka, Carbohydr. Res., 202, 177 (1990) |
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST) |