JCGGDB TOP Glycan Syntheses

Reaction

JCGG ID
JCGG-RAC0000257
Submitter
The Noguchi Institute
Reaction ID
R-0000-000257
Regist Date
2012/06/21 15:07:43
REACTANT
MOLECULE ID
JCGG-COM0000046 (Reaction Tree)
Reactant Type
1-Hydroxy sugar
Mol
1
MOLECULE ID
JCGG-COM0000096
Reactant Type
Alcohol
Mol
1
MOLECULE ID
JCGG-COM0000231
Reactant Type
Activator
Mol
0.05
PRODUCT
MOLECULE ID
JCGG-COM0000288 (Reaction Tree)
Skeleton
JCGG-STR032525
Product Type
alpha
Yield
35%(alpha/beta=57/43)
MOLECULE ID
JCGG-COM0000289 (Reaction Tree)
Skeleton
JCGG-STR031569
Product Type
beta
Yield
35%(alpha/beta=57/43)
MOLECULE ID
JCGG-COM0000290 (Reaction Tree)
Skeleton
JCGG-STR001328
Product Type
byproduct
Yield
4%
REACTION DETAIL
Reaction Time
12 hours
Reaction Temp
room temp
Solvent
CH2Cl2
Catalyst
Activator
Comment
anhydrous CaSO4 was included in the solvent.
Scheme 1
COMMENT
The PMID could not be found.
The alpha/beta ratio was determined by NMR.
REFERENCE
Reference Id
REF-0000-000012
Source
HETEROCYCLES, Vol. 77, No. 1, 2009, pp. 445 - 460
Doi
10.3987/COM-08-S(F)41

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