JCGGDB TOP Glycan Syntheses

Reaction

JCGG ID
JCGG-RAC0002858
Submitter
The Noguchi Institute
Reaction ID
R-0000-002858
Regist Date
2012/06/21 20:00:15
REACTANT
MOLECULE ID
JCGG-COM0003746 (Reaction Tree)
Mol
58 micro mole
MOLECULE ID
JCGG-COM0001281
Reactant Type
(CH2NH2)2
Mol
11.7 mmol
MOLECULE ID
JCGG-COM0000086
Reactant Type
Ac2O
Volume
1 mL
PRODUCT
MOLECULE ID
JCGG-COM0003748 (Reaction Tree)
Yield
75%
REACTION DETAIL
Reaction Time
2 hours, 0.5 hour
Reaction Temp
90 degree C, room temp
Solvent
n-BuOH (5mL), CH2Cl2/MeOH = 2mL/4mL
Comment
1) 17+(CH2NH2)2, 2) +Ac2O
COMMENT
Keywords: Biantennary, N-glycans, LacNAc, LacdiNAc, SPPS
There are multiple phases in this reaction.
REFERENCE
Reference Id
REF-0000-000371
Issn
Electronic
Doi
10.1021/jo200149d
PubMed ID
21612260
Journal Name
The Journal of organic chemistry. (2011) 76 (13): 5229-39.
Article Title
Synthesis of biantennary complex-type nonasaccharyl asn building blocks for solid-phase glycopeptide synthesis.
Author
Masashi, Hagiwara; Mizuki, Dohi; Yuko, Nakahara; Keiko, Komatsu; Yuya, Asahina; Akiharu, Ueki; Hironobu, Hojo; Yoshiaki, Nakahara; Yukishige, Ito
Affiliation
Department of Applied Biochemistry, Institute of Glycoscience, Tokai University, 4-1-1 Kitakaname, Hiratsuka-shi, Kanagawa 259-1292, Japan.
Reference Id
REF-0000-000372
Source
J. Org. Chem. 2011, 76, 5229-5239
Doi
10.1021/jo200149d

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