JCGGDB TOP Glycan Syntheses

Reaction

JCGG ID
JCGG-RAC0001607
Submitter
The Noguchi Institute
Reaction ID
R-0000-001607
Regist Date
2012/06/21 17:25:27
REACTANT
MOLECULE ID
JCGG-COM0002051 (Reaction Tree)
Mol
1.94 mmol
MOLECULE ID
JCGG-COM0001858
Reactant Type
HO(CH2)8COOMe
Mol
2.92 mmol
MOLECULE ID
JCGG-COM0000099
Reactant Type
BF3*OEt2 (in 7.0 mL of ClCH2CH2Cl/hexane)
Mol
1.06 mmol
PRODUCT
MOLECULE ID
JCGG-COM0002052 (Reaction Tree)
Yield
33%
REACTION DETAIL
Reaction Time
30 minutes
Reaction Temp
-40 degree C
Solvent
ClCH2CH2Cl/hexane = 1/1
Comment
2, HO(CH2)8COOMe, and MS 4A were mixed and stirred for 1 hour at before the reaction.
MS 4A was included in the solvent.
BF3*OEt2 was added dropwise.
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)