|
Glycan Syntheses |
JCGG ID |
JCGG-RAC0001080 | ||||
Submitter |
The Noguchi Institute | ||||
Reaction ID |
R-0000-001087
|
||||
Regist Date |
2012/06/21 16:38:27 | ||||
| REACTANT | |||||
|
|
|
||||
Reactant Type |
mannose type isomer | ||||
|
|
|
||||
Reactant Type |
NaOMe | ||||
| PRODUCT | |||||
MOLECULE ID |
|
|
|||
Yield |
64% | ||||
| REACTION DETAIL | |||||
Solvent |
MeOH | ||||
| COMMENT | |||||
| The procedure regarding this reaction is discussed in another paper in References. | |||||
| REFERENCE | |||||
Reference Id |
REF-0000-000048 | ||||
Issn |
|||||
PubMed ID |
11273599 | ||||
Journal Name |
Journal of the American Chemical Society. (2001) 123 (1): 35-48. | ||||
Article Title |
Total syntheses of tumor-related antigens N3: probing the feasibility limits of the glycal assembly method. | ||||
Author |
H M, Kim; I J, Kim; S J, Danishefsky | ||||
Affiliation |
Laboratory for Bioorganic Chemistry, Sloan-Kettering Institute for Cancer Research, 1275 York Ave., New York, New York 10021, USA. | ||||
Reference Id |
REF-0000-000049 | ||||
Source |
J. Am. Chem. Soc. 2001, 123, 35-48 | ||||
Doi |
10.1021/ja0022730 | ||||
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST)
|