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Glycan Syntheses |
JCGG ID |
JCGG-RAC0001221 | ||||
Submitter |
The Noguchi Institute | ||||
Reaction ID |
R-0000-001227
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Regist Date |
2012/06/21 16:46:02 | ||||
| REACTANT | |||||
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Mol |
2.06 mmol | ||||
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Reactant Type |
NaOMe | ||||
Mol |
spatula (small amount) | ||||
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Reactant Type |
NaH | ||||
Mol |
10.0 mmol | ||||
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Reactant Type |
BnBr | ||||
Mol |
4.53 mmol | ||||
| PRODUCT | |||||
MOLECULE ID |
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Yield |
78% | ||||
| REACTION DETAIL | |||||
Reaction Time |
16 hours (at least) | ||||
Reaction Temp |
NOT specified | ||||
Solvent |
DMF | ||||
Comment |
Before the reaction, 3 and NaOMe were dissolved in 30 mL of MeOH, and the solvent was evaporated in vacuo. | ||||
| COMMENT | |||||
| Keywords: galactal derivatives, 6-O-TIPS protection, trichloroacetimidates, Michael-type addition, 2-nitroglycals | |||||
| REFERENCE | |||||
Reference Id |
REF-0000-000063 | ||||
Issn |
|||||
Doi |
10.1021/jo061670b | ||||
PubMed ID |
17503844 | ||||
Journal Name |
The Journal of organic chemistry. (2007) 72 (12): 4367-77. | ||||
Article Title |
Glycal glycosylation and 2-nitroglycal concatenation, a powerful combination for mucin core structure synthesis. | ||||
Author |
Jürgen, Geiger; B Gopal, Reddy; Gottfried A, Winterfeld; R, Weber; M, Przybylski; R R, Schmidt | ||||
Affiliation |
Fachbereich Chemie, Universität Konstanz, Fach M 725, D - 78457 Konstanz, Germany. | ||||
Reference Id |
REF-0000-000064 | ||||
Source |
J. Org. Chem. 2007, 72, 4367-4377 | ||||
Doi |
10.1021/jo061670b | ||||
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST)
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