JCGGDB TOP Glycan Syntheses

Reaction

JCGG ID
JCGG-RAC0001609
Submitter
The Noguchi Institute
Reaction ID
R-0000-001609
Regist Date
2012/06/21 17:25:39
REACTANT
MOLECULE ID
JCGG-COM0002053 (Reaction Tree)
Mol
0.490 mmol
MOLECULE ID
JCGG-COM0001086
Reactant Type
BzCN (in DMF)
Mol
0.13 mmol
MOLECULE ID
JCGG-COM0000047
Reactant Type
Et3N (in DMF)
Volume
0.21 mL
PRODUCT
MOLECULE ID
JCGG-COM0002055 (Reaction Tree)
Yield
71%
REACTION DETAIL
Reaction Time
1 hour
Reaction Temp
-40 degree C
Solvent
DMF
Comment
The reaction condition (BzCN and Et3N) selectively acylates the primary alcohol. (C-6 hydroxy group)
NOTICE: The amount of the disaccharide exceeds that of BzCN.
COMMENT
Keywords: biological activity, carbohydrates, conformation analysis, lectins, synthesis design
REFERENCE
Reference Id
REF-0000-000189
Issn
Print
Doi
10.1002/chem.200400831
PubMed ID
15770712
Journal Name
Chemistry (Weinheim an der Bergstrasse, Germany). (2005) 11 (10): 3032-8.
Article Title
Synthesis and evaluation of 5-thio-L-fucose-containing oligosaccharide.
Author
Masayuki, Izumi; Osamu, Tsuruta; Yasuhiro, Kajihara; Shin, Yazawa; Hideya, Yuasa; Hironobu, Hashimoto
Affiliation
Department of Life Science, Graduate school of Bioscience and Biotechnology, Tokyo Institute of Technology, 4259 Nagatsuta, Yokohama 226-8501, Japan.masayuki.izumi@aist.go.jp
Reference Id
REF-0000-000190
Source
Chem. Eur. J. 2005, 11, 3032-3038
Doi
10.1002/chem.200400831

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