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Glycan Syntheses |
JCGG ID |
JCGG-RAC0002061 | ||||
Submitter |
The Noguchi Institute | ||||
Reaction ID |
R-0000-002061
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Regist Date |
2012/06/21 18:30:10 | ||||
| REACTANT | |||||
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Reactant Type |
intermediate | ||||
Mol |
88.36 to 94 micro mol | ||||
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Reactant Type |
I2 | ||||
Mol |
0.19 mmol | ||||
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Reactant Type |
pyridine | ||||
Volume |
1.8 mL | ||||
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Reactant Type |
H2O | ||||
Volume |
94 micro L | ||||
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Reactant Type |
TEAB | ||||
Volume |
2*5.0 mL | ||||
| PRODUCT | |||||
MOLECULE ID |
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Yield |
94%(at least) | ||||
| REACTION DETAIL | |||||
Reaction Time |
2 hours | ||||
Reaction Temp |
room temp | ||||
Solvent |
dry CH2Cl2 | ||||
Comment |
TEAB was added at the end of the reaction. | ||||
| COMMENT | |||||
| Keywords: alpha-D-glycosyl boranophosphate, phosphoramidite, condensation, boronation, terminal deprotection, Leishmania glycocalyx lipophosphoglycans | |||||
| REFERENCE | |||||
Reference Id |
REF-0000-000315 | ||||
Issn |
Electronic | ||||
Doi |
10.1021/jo102584g | ||||
PubMed ID |
21381786 | ||||
Journal Name |
The Journal of organic chemistry. (2011) 76 (8): 2648-59. | ||||
Article Title |
Synthesis of oligo(α-D-glycosyl phosphate) derivatives by a phosphoramidite method via boranophosphate intermediates. | ||||
Author |
Shoichi, Fujita; Natsuhisa, Oka; Fumiko, Matsumura; Takeshi, Wada | ||||
Affiliation |
Department of Medical Genome Sciences, Graduate School of Frontier Sciences, The University of Tokyo, Bioscience Building 702, 5-1-5 Kashiwanoha, Kashiwa, Chiba 277-8562, Japan. | ||||
Reference Id |
REF-0000-000316 | ||||
Source |
J. Org. Chem. 2011, 76, 2648-2659 | ||||
Doi |
10.1021/jo102584g | ||||
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST)
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