JCGGDB TOP Glycan Syntheses

Reaction

JCGG ID
 JCGG-RAC0002883
Submitter
 The Noguchi Institute
Reaction ID
 R-0000-002883
Regist Date
 2012/06/29 18:32:29
REACTANT
MOLECULE ID
 JCGG-COM0004262 (Reaction Tree)
Skeleton
JCGG-STR027560
MOLECULE ID
 JCGG-COM0004263 (Reaction Tree)
MOLECULE ID
 JCGG-COM0003517
Reactant Type
 Ph2SO
MOLECULE ID
 JCGG-COM0000761
Reactant Type
 Tf2O
MOLECULE ID
 JCGG-COM0002536
Reactant Type
 TTBP
PRODUCT
MOLECULE ID
 JCGG-COM0004264 (Reaction Tree)
Skeleton
JCGG-STR024639
Yield
 75%
REACTION DETAIL
Reaction Time
 NOT specified
Reaction Temp
 -78 degree C
Solvent
 CH2Cl2
Comment
 Very few were described regarding this reaction.
COMMENT
Keywords: diastereoselective synthesis, critical interplay, 2-deoxy-beta-glycopyranosides, beta-mannopyranosides, alpha-sialosides, alpha-glucopyranosides, beta-arabinofuranosides
REFERENCE
Reference Id
 REF-0000-000373
Issn
 Electronic
Doi
 10.1021/jo2017026
PubMed ID
 21919522
Journal Name
 The Journal of organic chemistry. (2011) 76 (22): 9193-209.
Article Title
 Methodology development and physical organic chemistry: a powerful combination for the advancement of glycochemistry.
Author
 David, Crich
Affiliation
 Department of Chemistry, Wayne State University, Detroit, Michigan 48202, USA. dcrich@chem.wayne.edu
Reference Id
 REF-0000-000374
Source
 J. Org. Chem. 2011, 76, 9193-9209
Doi
 10.1021/jo2017026
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST)