Linked Life Data

19300809

Source:http://linkedlifedata.com/resource/pubmed/id/19300809

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
7
pubmed:dateCreated
2009-3-20
pubmed:abstractText
A convenient and efficient method for selective replacement of the primary hydroxyl groups of sugars by chlorine with concomitant O-formylation, compatible with the presence of a variety of functional groups, has been developed using the Vilsmeier-Haack reaction. Sugars having free primary hydroxyl groups mostly afforded the chloro-O-formylated product while sugars devoid of primary hydroxyl groups yielded only O-formylated products.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
1477-0539
pubmed:author
pubmed:issnType
Electronic
pubmed:day
7
pubmed:volume
7
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1280-3
pubmed:meshHeading
pubmed:year
2009
pubmed:articleTitle
Reaction of carbohydrates with Vilsmeier reagent: a tandem selective chloro O-formylation of sugars.
pubmed:affiliation
Bio-organic Chemistry Division, Indian Institute of Integrative Medicine, Canal Road, Jammu, India-180001.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't