JCGGDB TOP Glycan Syntheses

Reaction

JCGG ID
JCGG-RAC0001264
Submitter
The Noguchi Institute
Reaction ID
R-0000-001264
Regist Date
2012/06/21 16:47:49
REACTANT
MOLECULE ID
JCGG-COM0001416 (Reaction Tree)
MOLECULE ID
JCGG-COM0000414
Reactant Type
H2 (gas, 75 psi)
MOLECULE ID
JCGG-COM0000979
Reactant Type
pyridine (solvent)
Volume
2.66 mL
MOLECULE ID
JCGG-COM0000086
Reactant Type
Ac2O (solvent)
Volume
1.33 mL
PRODUCT
MOLECULE ID
JCGG-COM0001417 (Reaction Tree)
Skeleton
JCGG-STR015955
Yield
79%
REACTION DETAIL
Reaction Time
24 hours, overnight
Reaction Temp
NOT specified, NOT specified
Solvent
EtOH, pyridine/Ac2O = 2/1
Catalyst
platinized Raney nickel T4 (first phase)
Comment
1) 34b+H2, 2) solvent change
COMMENT
Keywords: galactal derivatives, 6-O-TIPS protection, trichloroacetimidates, Michael-type addition, 2-nitroglycals
There are multiple phases in this reaction.
REFERENCE
Reference Id
REF-0000-000063
Issn
Print
Doi
10.1021/jo061670b
PubMed ID
17503844
Journal Name
The Journal of organic chemistry. (2007) 72 (12): 4367-77.
Article Title
Glycal glycosylation and 2-nitroglycal concatenation, a powerful combination for mucin core structure synthesis.
Author
Jürgen, Geiger; B Gopal, Reddy; Gottfried A, Winterfeld; R, Weber; M, Przybylski; R R, Schmidt
Affiliation
Fachbereich Chemie, Universität Konstanz, Fach M 725, D - 78457 Konstanz, Germany.
Reference Id
REF-0000-000064
Source
J. Org. Chem. 2007, 72, 4367-4377
Doi
10.1021/jo061670b

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