JCGGDB TOP Glycan Syntheses

Reaction

JCGG ID
JCGG-RAC0001318
Submitter
The Noguchi Institute
Reaction ID
R-0000-001318
Regist Date
2012/06/21 16:50:26
REACTANT
MOLECULE ID
JCGG-COM0001490 (Reaction Tree)
Mol
1.32 mmol
MOLECULE ID
JCGG-COM0000889
Reactant Type
BnOH
Mol
2.64 mmol
MOLECULE ID
JCGG-COM0000099
Reactant Type
BF3*OEt2
Mol
0.197 + 2.76 + 3.16 mmol
PRODUCT
MOLECULE ID
JCGG-COM0001491 (Reaction Tree)
Yield
92%
REACTION DETAIL
Reaction Time
6 hours
Reaction Temp
0 degree C
Solvent
CH2Cl2
Comment
MS 4A was included in the solvent.
BF3*OEt2 was added three times. (0 hour, 2 hours, and 4 hours)
COMMENT
Keywords: stereoselective synthesis, mycobacterial arabinan, arabinofuranosyl donors, arabinofuranosylation, TIDPS
REFERENCE
Reference Id
REF-0000-000067
Issn
Print
Doi
10.1021/ol062198j
PubMed ID
17107063
Journal Name
Organic letters. (2006) 8 (24): 5525-8.
Article Title
Stereoselective synthesis of a fragment of mycobacterial arabinan.
Author
Akihiro, Ishiwata; Hiroko, Akao; Yukishige, Ito
Affiliation
RIKEN (Institute of Physical and Chemical Research), Wako-shi, Saitama 351-0198, Japan.
Reference Id
REF-0000-000068
Source
ORGANIC LETTERS, 2006, Vol. 8, No. 24, 5525-5528
Doi
10.1021/ol062198j

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