JCGGDB TOP Glycan Syntheses

Reaction

JCGG ID
JCGG-RAC0001347
Submitter
The Noguchi Institute
Reaction ID
R-0000-001348
Regist Date
2012/06/21 16:52:04
REACTANT
MOLECULE ID
JCGG-COM0001541 (Reaction Tree)
Reactant Type
acceptor
Mol
14.9 micro mol
MOLECULE ID
JCGG-COM0001482 (Reaction Tree)
Reactant Type
donor
Mol
37.1 micro mol
MOLECULE ID
JCGG-COM0000129
Reactant Type
NIS
Mol
55.8 micro mol
MOLECULE ID
JCGG-COM0000624
Reactant Type
AgOTf
Mol
5.84 micro mol
PRODUCT
MOLECULE ID
JCGG-COM0001542 (Reaction Tree)
Yield
94%
REACTION DETAIL
Reaction Time
3 hours
Reaction Temp
-40 degree C
Solvent
dry CH2Cl2
Comment
Freshly dried MS3A was included in the solvent.
The acceptor, the donor, and MS3A were mixed at room temperature before the reaction.
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)