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Glycan Syntheses |
JCGG ID |
JCGG-RAC0001247 | ||||
Submitter |
The Noguchi Institute | ||||
Reaction ID |
R-0000-001182
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Regist Date |
2012/06/21 16:43:39 | ||||
| REACTANT | |||||
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Reactant Type |
TBSOTf | ||||
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Reactant Type |
2,6-lutidine | ||||
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Reactant Type |
NaOMe | ||||
| PRODUCT | |||||
MOLECULE ID |
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Yield |
53%(at least) | ||||
| REACTION DETAIL | |||||
Solvent |
CH2Cl2, MeOH | ||||
Comment |
1) 9+TBSOTf, 2,6-lutidine, 2) +NaOMe | ||||
| Very few were described regarding this reaction. | |||||
| COMMENT | |||||
| Keywords: prostate specific antigen, PSA, N-linked glycan, peptide backbone, antibody, cancer, amino acid, keyhole limpet hemocyanin, KLH | |||||
| There are two phases in this reaction. | |||||
| REFERENCE | |||||
Reference Id |
REF-0000-000061 | ||||
Issn |
Electronic | ||||
Doi |
10.1021/ja8028137 | ||||
PubMed ID |
18798614 | ||||
Journal Name |
Journal of the American Chemical Society. (2008) 130 (41): 13598-607. | ||||
Article Title |
Toward a prostate specific antigen-based prostate cancer diagnostic assay: preparation of keyhole limpet hemocyanin-conjugated normal and transformed prostate specific antigen fragments. | ||||
Author |
Vadim Y, Dudkin; Justin S, Miller; Anna S, Dudkina; Christophe, Antczak; David A, Scheinberg; Samuel J, Danishefsky | ||||
Affiliation |
Laboratory for Bioorganic Chemistry, Sloan-Kettering Institute for Cancer Research, 1275 York Avenue, New York, New York 10065, USA. | ||||
Reference Id |
REF-0000-000062 | ||||
Source |
J. AM. CHEM. SOC. 2008, 130, 13598-13607 | ||||
Doi |
10.1021/ja8028137 | ||||
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST)
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