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Glycan Syntheses |
JCGG ID |
JCGG-RAC0002792 | ||||
Submitter |
The Noguchi Institute | ||||
Reaction ID |
R-0000-002792
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Regist Date |
2012/06/21 19:49:41 | ||||
| REACTANT | |||||
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Mol |
41 micro mole | ||||
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Reactant Type |
AcOH | ||||
Mol |
0.16 mmol | ||||
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Reactant Type |
TBAF (1 M in THF) | ||||
Mol |
82 micro mole | ||||
| PRODUCT | |||||
MOLECULE ID |
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Product Type |
intermediate | ||||
Yield |
96% | ||||
| REACTION DETAIL | |||||
Reaction Time |
3 hours | ||||
Reaction Temp |
0 degree C | ||||
Solvent |
THF (1mL) | ||||
| COMMENT | |||||
| Keywords: mannuronic acids, mannopyranosides, mannopyranosyl methyl uronate, all-cis-linked tetrasaccharide | |||||
| REFERENCE | |||||
Reference Id |
REF-0000-000367 | ||||
Issn |
Electronic | ||||
Doi |
10.1021/jo201179p | ||||
PubMed ID |
21793528 | ||||
Journal Name |
The Journal of organic chemistry. (2011) 76 (18): 7301-15. | ||||
Article Title |
Stereoselective synthesis of 2,3-diamino-2,3-dideoxy-β-D-mannopyranosyl uronates. | ||||
Author |
Marthe T C, Walvoort; Gert-Jan, Moggré; Gerrit, Lodder; Herman S, Overkleeft; Jeroen D C, Codée; Gijsbert A, van der Marel | ||||
Affiliation |
Leiden Institute of Chemistry, Leiden University, P.O. Box 9502, 2300 RA Leiden, The Netherlands. | ||||
Reference Id |
REF-0000-000368 | ||||
Source |
J. Org. Chem. 2011, 76, 7301-7315 | ||||
Doi |
10.1021/jo201179p | ||||
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST)
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