JCGGDB TOP Glycan Syntheses

Reaction

JCGG ID
JCGG-RAC0002429
Submitter
The Noguchi Institute
Reaction ID
R-0000-002429
Regist Date
2012/06/21 19:13:34
REACTANT
MOLECULE ID
JCGG-COM0003157 (Reaction Tree)
Skeleton
JCGG-STR032527
Mol
1.0 equiv.
MOLECULE ID
JCGG-COM0001109
Reactant Type
thiophenol
Mol
1.2 equiv.
MOLECULE ID
JCGG-COM0000009
Reactant Type
TMSOTf
Mol
0.8 equiv.
PRODUCT
MOLECULE ID
JCGG-COM0003158 (Reaction Tree)
Yield
85%
REACTION DETAIL
Reaction Time
2 hours
Reaction Temp
NOT specified
Solvent
CH2Cl2
Comment
MS 4A was included in the solvent.
COMMENT
Keywords: acylation, pivaloylation, pivaloyl chloride, esterifying, regioisomers
REFERENCE
Reference Id
REF-0000-000341
Issn
Electronic
PubMed ID
11672212
Journal Name
The Journal of organic chemistry. (1998) 63 (17): 6035-6038.
Article Title
Regioselective Acylation of Hexopyranosides with Pivaloyl Chloride.
Author
Lu, Jiang; Tak-Hang, Chan
Affiliation
Department of Chemistry, McGill University, Montréal, Québec H3A 2K6, Canada.
Reference Id
REF-0000-000342
Source
J. Org. Chem. 1998, 63, 6035-6038
Doi
10.1021/jo980294v

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