JCGGDB TOP Glycan Syntheses

Reaction

JCGG ID
 JCGG-RAC0001320
Submitter
 The Noguchi Institute
Reaction ID
 R-0000-001320
Regist Date
 2012/06/21 16:50:32
REACTANT
MOLECULE ID
 JCGG-COM0001493 (Reaction Tree)
Reactant Type
 donor
Mol
 NOT specified
MOLECULE ID
 JCGG-COM0001494 (Reaction Tree)
Reactant Type
 acceptor
Mol
 1.0 equiv.
MOLECULE ID
 JCGG-COM0000129
Reactant Type
 NIS
Mol
 1.2 to 2.0 equiv.
MOLECULE ID
 JCGG-COM0000624
Reactant Type
 AgOTf
Mol
 0.3 to 1.0 equiv.
PRODUCT
MOLECULE ID
 JCGG-COM0001495 (Reaction Tree)
Product Type
 alpha
Yield
 97%(alpha/beta=9.4/1)
MOLECULE ID
 JCGG-COM0001496 (Reaction Tree)
Skeleton
JCGG-STR006602
Product Type
 beta
Yield
 97%(alpha/beta=9.4/1)
REACTION DETAIL
Reaction Time
 1 hour
Reaction Temp
 -78 degree C
Solvent
 CH2Cl2
COMMENT
Keywords: stereoselective synthesis, mycobacterial arabinan, arabinofuranosyl donors, arabinofuranosylation, TIDPS
The details regarding this reaction are described in another paper in References.
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)