JCGGDB TOP Glycan Syntheses

Reaction

JCGG ID
 JCGG-RAC0002878
Submitter
 The Noguchi Institute
Reaction ID
 R-0000-002878
Regist Date
 2012/06/29 18:31:22
REACTANT
MOLECULE ID
 JCGG-COM0004245 (Reaction Tree)
Skeleton
JCGG-STR032527
MOLECULE ID
 JCGG-COM0004246
Reactant Type
 Bu3SnD
MOLECULE ID
 JCGG-COM0002547
Reactant Type
 AIBN
MOLECULE ID
 JCGG-COM0002446
Reactant Type
 SiO2
PRODUCT
MOLECULE ID
 JCGG-COM0004247 (Reaction Tree)
Yield
 31%
MOLECULE ID
 JCGG-COM0004248 (Reaction Tree)
Skeleton
JCGG-STR032527
Yield
 35%
MOLECULE ID
 JCGG-COM0004249 (Reaction Tree)
Yield
 22%
REACTION DETAIL
Reaction Time
 NOT specified, NOT specified
Reaction Temp
 heating, NOT specified
Solvent
 C6H6, NOT specified
Comment
 1) +all except SiO2, 2) +SiO2
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
There are multiple phases in this reaction.
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)