JCGG ID |
JCGG-RAC0002661 | ||||
Submitter |
The Noguchi Institute | ||||
Reaction ID |
R-0000-002661 | ||||
Regist Date |
2012/06/21 19:35:58 | ||||
REACTANT | |||||
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Mol |
22.7 mmol | ||||
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Reactant Type |
HF*pyridine (70% solution in THF/pyridine = 65/35, 25 mL) | ||||
Mol |
158.0 mmol | ||||
PRODUCT | |||||
MOLECULE ID |
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Yield |
86% | ||||
REACTION DETAIL | |||||
Reaction Time |
30 minutes, 1 hour | ||||
Reaction Temp |
0 degree C, room temp | ||||
Solvent |
THF (350mL), THF (350mL) | ||||
Comment |
1) +all, 2) temperature change | ||||
COMMENT | |||||
Keywords: building block, ceramides, glycolipids, galactosyl-phytosphingosine, KRN7000 | |||||
There are multiple phases in this reaction. | |||||
REFERENCE | |||||
Reference Id |
REF-0000-000361 | ||||
Issn |
Electronic | ||||
Doi |
10.1021/jo102064p | ||||
PubMed ID |
21155575 | ||||
Journal Name |
The Journal of organic chemistry. (2011) 76 (1): 320-3. | ||||
Article Title |
Synthesis of a versatile building block for the preparation of 6-N-derivatized α-galactosyl ceramides: rapid access to biologically active glycolipids. | ||||
Author |
Peter J, Jervis; Liam R, Cox; Gurdyal S, Besra | ||||
Affiliation |
School of Biosciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, United Kingdom. | ||||
Reference Id |
REF-0000-000362 | ||||
Source |
J. Org. Chem. 2011, 76, 320-323 | ||||
Doi |
10.1021/jo102064p |
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST) |