JCGGDB TOP Glycan Syntheses

Reaction

JCGG ID
JCGG-RAC0000749
Submitter
The Noguchi Institute
Reaction ID
R-0000-000749
Regist Date
2012/06/21 16:21:41
REACTANT
MOLECULE ID
JCGG-COM0000835 (Reaction Tree)
Skeleton
JCGG-STR031569
MOLECULE ID
JCGG-COM0000708
Reactant Type
NaBH3CN
MOLECULE ID
JCGG-COM0000110
Reactant Type
TFA
PRODUCT
MOLECULE ID
JCGG-COM0000836 (Reaction Tree)
Skeleton
JCGG-STR031569
Yield
89%
MOLECULE ID
JCGG-COM0000837 (Reaction Tree)
Skeleton
JCGG-STR031569
Yield
8%
REACTION DETAIL
Reaction Temp
room temp
Solvent
DMF
Comment
MS 3A was included in the solvent.
The reactants were mixed at 0 degree in Celsius before stirred at room temperature.
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)