JCGGDB TOP Glycan Syntheses

Reaction

JCGG ID
JCGG-RAC0002756
Submitter
The Noguchi Institute
Reaction ID
R-0000-002756
Regist Date
2012/06/21 19:45:49
REACTANT
MOLECULE ID
JCGG-COM0003599 (Reaction Tree)
Skeleton
JCGG-STR032527
Mol
0.134 mmol
PRODUCT
MOLECULE ID
JCGG-COM0003600 (Reaction Tree)
Skeleton
JCGG-STR032527
Yield
87%
MOLECULE ID
JCGG-COM0003601 (Reaction Tree)
Yield
43%
MOLECULE ID
JCGG-COM0003602 (Reaction Tree)
Yield
5%
MOLECULE ID
JCGG-COM0003603 (Reaction Tree)
Yield
11%
REACTION DETAIL
Reaction Time
4.5 hours
Reaction Temp
20 to 30 degree C
Solvent
MeOH (26.7mL)
Reaction Type
photochemical cleavage
Comment
irradiation of UV light
The reaction was conducted in a Pyrex test tube kept in a water bath.
COMMENT
Keywords: trityl, photolabile, PPGs, electron-donating substituents, m-dimethylamino, photochemical deprotection
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)