Linked Life Data

21341742

Source:http://linkedlifedata.com/resource/pubmed/id/21341742

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2011-3-11
pubmed:abstractText
All stereoisomers of a highly functionalized 2,3-unsaturated C-glycoside can be accessed in 10-100 g quantities from readily available starting materials and reagents in 3-7 steps. These chiral scaffolds contain three stereogenic centers along with orthogonally protected functional groups for downstream reactivity.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
1520-6904
pubmed:author
pubmed:issnType
Electronic
pubmed:day
18
pubmed:volume
76
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1898-901
pubmed:meshHeading
pubmed:year
2011
pubmed:articleTitle
Large-scale synthesis of all stereoisomers of a 2,3-unsaturated C-glycoside scaffold.
pubmed:affiliation
Chemical Biology Platform, The Broad Institute of MIT and Harvard, 7 Cambridge Center, Cambridge, Massachusetts 02142, USA.
pubmed:publicationType
Journal Article, Research Support, N.I.H., Extramural