JCGGDB TOP Glycan Syntheses

Reaction

JCGG ID
JCGG-RAC0000607
Submitter
The Noguchi Institute
Reaction ID
R-0000-000607
Regist Date
2012/06/21 16:14:49
REACTANT
MOLECULE ID
JCGG-COM0000629 (Reaction Tree)
Mol
18.83 mmol
MOLECULE ID
JCGG-COM0000630
Reactant Type
MsOH
Mol
46.25 mmol
MOLECULE ID
JCGG-COM0000631
Reactant Type
BnOCH2COONSu
Mol
23.78 mmol
MOLECULE ID
JCGG-COM0000047
Reactant Type
TEA
Volume
4mL
PRODUCT
MOLECULE ID
JCGG-COM0000632 (Reaction Tree)
Yield
75%
REACTION DETAIL
Reaction Time
24 hours, 24 hours
Reaction Temp
60 degree C, room temp
Solvent
dry MeOH, CH3CN/H2O = 15/1
Comment
1) 3+MsOH, 2) +BnOCH2COONSu, TEA
COMMENT
There are two phases in this reaction.
The product was used for the next reaction.
REFERENCE
Reference Id
REF-0000-000028
Issn
Electronic
Doi
10.1021/jm8000696
PubMed ID
18841881
Journal Name
Journal of medicinal chemistry. (2008) 51 (21): 6665-81.
Article Title
Design, synthesis, and structure-affinity relationships of novel series of sialosides as CD22-specific inhibitors.
Author
Hajjaj H M, Abdu-Allah; Taichi, Tamanaka; Jie, Yu; Lu, Zhuoyuan; Magesh, Sadagopan; Takahiro, Adachi; Takeshi, Tsubata; Soerge, Kelm; Hideharu, Ishida; Makoto, Kiso
Affiliation
Department of Applied Bio-organic Chemistry, The United Graduate School of Agricultural Sciences, Gifu University, Gifu 501-1193, Japan.
Reference Id
REF-0000-000029
Source
J. Med. Chem., 2008, 51, 6665-6681
Doi
10.1021/jm8000696

©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST)