JCGGDB TOP Glycan Syntheses

Reaction

JCGG ID
JCGG-RAC0002720
Submitter
The Noguchi Institute
Reaction ID
R-0000-002720
Regist Date
2012/06/21 19:42:46
REACTANT
MOLECULE ID
JCGG-COM0003554 (Reaction Tree)
Reactant Type
2-(diphenyl(3-phenylpropoxy)methyl)-4-methoxyphenol
Mol
0.40 mmol
MOLECULE ID
JCGG-COM0002100
Reactant Type
NaH
Mol
0.48 mmol
MOLECULE ID
JCGG-COM0001727
Reactant Type
MeI
Mol
4.00 mmol
PRODUCT
MOLECULE ID
JCGG-COM0003555 (Reaction Tree)
Yield
68%
REACTION DETAIL
Reaction Time
3.5 hours
Reaction Temp
0 degree C
Solvent
THF (0.4mL)
COMMENT
Keywords: trityl, photolabile, PPGs, electron-donating substituents, m-dimethylamino, photochemical deprotection
The reaction is explained in text only.
REFERENCE
Reference Id
REF-0000-000365
Issn
Electronic
Doi
10.1021/jo200692c
PubMed ID
21612261
Journal Name
The Journal of organic chemistry. (2011) 76 (15): 5873-81.
Article Title
Development of trityl-based photolabile hydroxyl protecting groups.
Author
Lei, Zhou; Haishen, Yang; Pengfei, Wang
Affiliation
Department of Chemistry, University of Alabama at Birmingham, 901 14th Street South, Birmingham, Alabama 35294, USA.
Reference Id
REF-0000-000366
Source
J. Org. Chem. 2011, 76, 5873-5881
Doi
10.1021/jo200692c

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