JCGGDB TOP Glycan Syntheses

Reaction

JCGG ID
JCGG-RAC0000752
Submitter
The Noguchi Institute
Reaction ID
R-0000-000752
Regist Date
2012/06/21 16:21:50
REACTANT
MOLECULE ID
JCGG-COM0000841 (Reaction Tree)
Mol
0.585 mmol
MOLECULE ID
JCGG-COM0000521
Reactant Type
CCl3CN
Mol
11.7 mmol
MOLECULE ID
JCGG-COM0000842
Reactant Type
K2CO3
Mol
1.76 mmol
PRODUCT
MOLECULE ID
JCGG-COM0000843 (Reaction Tree)
Skeleton
JCGG-STR032525
Product Type
alpha
Yield
40%
MOLECULE ID
JCGG-COM0000844 (Reaction Tree)
Skeleton
JCGG-STR031569
Product Type
beta
Yield
53%
REACTION DETAIL
Reaction Time
3 hours
Reaction Temp
room temp
Solvent
CH2Cl2
COMMENT
REFERENCE
Reference Id
REF-0000-000035
Issn
Electronic
Doi
10.1021/jo8027888
PubMed ID
19296672
Journal Name
The Journal of organic chemistry. (2009) 74 (8): 3009-23.
Article Title
Ganglioside GQ1b: efficient total synthesis and the expansion to synthetic derivatives to elucidate its biological roles.
Author
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. aimamura@ualberta.ca
Reference Id
REF-0000-000036
Source
J. Org. Chem. 2009, 74, 3009-3023
Doi
10.1021/jo8027888

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