JCGG ID |
JCGG-RAC0002149 | ||||
Submitter |
The Noguchi Institute | ||||
Reaction ID |
R-0000-002149 | ||||
Regist Date |
2012/06/21 18:41:24 | ||||
REACTANT | |||||
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|
||||
Mol |
0.018 mmol | ||||
|
|
||||
Reactant Type |
TBAF (1 M in THF) | ||||
Mol |
0.363 mmol | ||||
PRODUCT | |||||
MOLECULE ID |
|
|
|||
Product Type |
intermediate | ||||
Yield |
95%(at least) | ||||
REACTION DETAIL | |||||
Reaction Time |
10 hours | ||||
Reaction Temp |
room temp | ||||
Solvent |
THF | ||||
COMMENT | |||||
Keywords: mannose-6-phosphate, M6P, N-linked glycans, eukaryotic cells, N-acetylglucosamine, GlcNAc, sequential deprotection | |||||
REFERENCE | |||||
Reference Id |
REF-0000-000321 | ||||
Issn |
Electronic | ||||
Doi |
10.1021/jo2010999 | ||||
PubMed ID |
21955083 | ||||
Journal Name |
The Journal of organic chemistry. (2011) 76 (21): 8682-9. | ||||
Article Title |
Chemical synthesis of N-linked glycans carrying both mannose-6-phosphate and GlcNAc-mannose-6-phosphate motifs. | ||||
Author |
Yunpeng, Liu; Gong, Chen | ||||
Affiliation |
Department of Chemistry, The Pennsylvania State University, University Park, Pennsylvania 16802, United States. | ||||
Reference Id |
REF-0000-000322 | ||||
Source |
J. Org. Chem., 2011, 76 (21), pp 8682-8689 | ||||
Doi |
10.1021/jo2010999 |
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST) |