JCGGDB TOP Glycan Syntheses

Reaction

JCGG ID
JCGG-RAC0000529
Submitter
The Noguchi Institute
Reaction ID
R-0000-000530
Regist Date
2012/06/21 16:11:04
REACTANT
MOLECULE ID
JCGG-COM0000520 (Reaction Tree)
Mol
60 micro mole
MOLECULE ID
JCGG-COM0000517
Reactant Type
ClP(OEt)2
Mol
151 micro mole
MOLECULE ID
JCGG-COM0000426
Reactant Type
DIEA
Mol
181 micro mole
PRODUCT
MOLECULE ID
JCGG-COM0000526 (Reaction Tree)
Product Type
alpha
Yield
87%(alpha/beta=5.5/1)
MOLECULE ID
JCGG-COM0000527 (Reaction Tree)
Product Type
beta
Yield
87%(alpha/beta=5.5/1)
REACTION DETAIL
Reaction Time
1 hour
Reaction Temp
room temp
Solvent
CH3CN
Comment
The reactants were mixed at 0 degree in Celsius before stirred at room temperature.
COMMENT
REFERENCE
Reference Id
REF-0000-000021
Issn
Electronic
Doi
10.1016/j.carres.2009.06.009
PubMed ID
19560125
Journal Name
Carbohydrate research. (2009) 344 (12): 1453-63.
Article Title
Study on systematizing the synthesis of the a-series ganglioside glycans GT1a, GD1a, and GM1 using the newly developed N-Troc-protected GM3 and GalN intermediates.
Author
Tatsuya, Komori; Akihiro, Imamura; Hiromune, Ando; Hideharu, Ishida; Makoto, Kiso
Affiliation
Department of Applied Bioorganic Chemistry, Faculty of Applied Biological Sciences, Gifu University, 1-1 Yanagido, Gifu-shi, Gifu 501-1193, Japan.
Reference Id
REF-0000-000022
Source
Carbohydrate Research, 344 (2009), 1453-1463
Doi
10.1016/j.carres.2009.06.009

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