Linked Life Data

11893203

Source:http://linkedlifedata.com/resource/pubmed/id/11893203

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2002-3-14
pubmed:abstractText
[structure: see text] Bifunctional macrolides projecting an anchor group to the right or left spatial position of the lactone ring were synthesized. The regioselectivity of the key [3 + 2] cycloaddition process was controlled by the remote cladinose group attached to the C-3 position. These conformationally constrained molecules were employed as molecular probes to study the ribosomal binding sites of bifunctional macrolide antibiotics.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
1523-7060
pubmed:author
pubmed:issnType
Print
pubmed:day
21
pubmed:volume
4
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
987-90
pubmed:dateRevised
2003-11-14
pubmed:meshHeading
pubmed:year
2002
pubmed:articleTitle
Regioselective synthesis of bifunctional macrolides for probing ribosomal binding.
pubmed:affiliation
Infectious Disease Research, Abbott Laboratories, D47P, AP52, 200 Abbott Park Road, Abbott Park, Illinois 60064, USA. zhenkun.ma@abbott.com
pubmed:publicationType
Journal Article