JCGGDB TOP Glycan Syntheses

Reaction

JCGG ID
JCGG-RAC0001660
Submitter
The Noguchi Institute
Reaction ID
R-0000-001660
Regist Date
2012/06/21 17:33:27
REACTANT
MOLECULE ID
JCGG-COM0002120 (Reaction Tree)
Reactant Type
bromide
Mol
0.5 mmol
MOLECULE ID
JCGG-COM0002121
Reactant Type
alcohol
Volume
0.5 mL
MOLECULE ID
JCGG-COM0000032
Reactant Type
AgClO4
Weight
15 mg
MOLECULE ID
JCGG-COM0001699
Reactant Type
Ag2CO3
Weight
150 mg
PRODUCT
MOLECULE ID
JCGG-COM0002122 (Reaction Tree)
Yield
81%
REACTION DETAIL
Reaction Time
1 hour, 20 minutes, 1 + 6 hours
Reaction Temp
20 degree C, 20 degree C, 20 degree C
Solvent
PhCH3/CH2Cl2 = 1/1, PhCH3/CH2Cl2 = 1/1, PhCH3/CH2Cl2 = 1/1
Comment
1) alcohol+MS 4A, Ag2CO3, 2) +AgClO4, 3) +bromide
MS 4A was included in the solvent.
The reaction was conducted with exclusion of light. (first step)
The bromide was added dropwise over 1 hour. (third step)
COMMENT
Keywords: synthesis of glycopeptide, O-glycan
There are multiple steps in this reaction.
REFERENCE
Reference Id
REF-0000-000073
Source
第4版 実験化学講座 (26), 丸善
Reference Id
REF-0000-000074
Source
ISBN 4-621-03702-1
Reference Id
REF-0000-000194
Source
H. Paulsen and M. Paal, Carbohydr. Res., 135, 53 (1984) ; H. Paulsen and M. Paal, ibid., 135, 71 (1984)

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