JCGG ID |
JCGG-RAC0001231 | ||||
Submitter |
The Noguchi Institute | ||||
Reaction ID |
R-0000-001237 | ||||
Regist Date |
2012/06/21 16:46:31 | ||||
REACTANT | |||||
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|
||||
Mol |
4.2 mmol | ||||
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|
||||
Mol |
6.3 mmol | ||||
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|
||||
Reactant Type |
Sn(OTf)2 (in 3mL of MeCN) | ||||
Mol |
0.26 mmol | ||||
PRODUCT | |||||
MOLECULE ID |
|
|
|||
Product Type |
alpha | ||||
Yield |
47% | ||||
MOLECULE ID |
|
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|||
Product Type |
beta | ||||
Yield |
5% | ||||
REACTION DETAIL | |||||
Reaction Time |
30 minutes | ||||
Reaction Temp |
0 degree C | ||||
Solvent |
CH2Cl2/Et2O = 1/2 | ||||
Comment |
Sn(OTf)2 was added dropwise. | ||||
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) |