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Glycan Syntheses |
JCGG ID |
JCGG-RAC0002235 | ||||
Submitter |
The Noguchi Institute | ||||
Reaction ID |
R-0000-002235
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Regist Date |
2012/06/21 18:53:08 | ||||
| REACTANT | |||||
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Mol |
1.2 mmol | ||||
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Reactant Type |
NaBH3CN | ||||
Mol |
10.4 mmol | ||||
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Reactant Type |
HCl (4 N in dioxane) | ||||
Mol |
16 mmol | ||||
| PRODUCT | |||||
MOLECULE ID |
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Yield |
80% | ||||
| REACTION DETAIL | |||||
Reaction Time |
2 hours | ||||
Reaction Temp |
0 degree C | ||||
Solvent |
anhydrous THF | ||||
Comment |
Powdered molecular sieves was included in the solvent. | ||||
| HCl was added dropwise. | |||||
| COMMENT | |||||
| Keywords: stereoselectivity, 2-azido-2-deoxygalactosyl donors, acetyl groups, temperature, computational methods | |||||
| REFERENCE | |||||
Reference Id |
REF-0000-000327 | ||||
Issn |
Electronic | ||||
Doi |
10.1021/jo1025157 | ||||
PubMed ID |
21574599 | ||||
Journal Name |
The Journal of organic chemistry. (2011) 76 (13): 5207-18. | ||||
Article Title |
Study of the stereoselectivity of 2-azido-2-deoxygalactosyl donors: remote protecting group effects and temperature dependency. | ||||
Author |
Jane, Kalikanda; Zhitao, Li | ||||
Affiliation |
Department of Chemistry, Binghamton University, Binghamton, New York 13902, United States. | ||||
Reference Id |
REF-0000-000328 | ||||
Source |
J. Org. Chem. 2011, 76, 5207-5218 | ||||
Doi |
10.1021/jo1025157 | ||||
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST)
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