JCGGDB TOP Glycan Syntheses

Reaction

JCGG ID
JCGG-RAC0001307
Submitter
The Noguchi Institute
Reaction ID
R-0000-001307
Regist Date
2012/06/21 16:49:58
REACTANT
MOLECULE ID
JCGG-COM0001475 (Reaction Tree)
Mol
76.85 mmol
MOLECULE ID
JCGG-COM0001476
Reactant Type
para-thiocresol
Mol
96.05 mmol
MOLECULE ID
JCGG-COM0000099
Reactant Type
BF3*OEt2
Mol
390 mmol
PRODUCT
MOLECULE ID
JCGG-COM0001477 (Reaction Tree)
Yield
86%
REACTION DETAIL
Reaction Time
30 minutes
Reaction Temp
0 degree C
Solvent
CH2Cl2
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)