Source:http://linkedlifedata.com/resource/pubmed/id/20544751
Switch to
| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
28
|
| pubmed:dateCreated |
2010-7-26
|
| pubmed:abstractText |
The interaction of [Ru(eta(6)-C(10)H(8))(Cp)](+) (Cp=C(5)H(5)) with aromatic amino acids (L-phenylalanine, L-tyrosine, L-tryptophane, D-phenylglycine, and L-threo-3-phenylserine) under visible-light irradiation gives the corresponding [Ru(eta(6)-amino acid)(Cp)](+) complexes in near-quantitative yield. The reaction proceeds in air at room temperature in water and tolerates the presence of non-aromatic amino acids (except those which are sulfur containing), monosaccharides, and nucleotides. The complex [Ru(eta(6)-C(10)H(8))(Cp)](+) was also used for selective labeling of Tyr and Phe residues of small peptides, namely, angiotensin I and II derivatives.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Jul
|
| pubmed:issn |
1521-3765
|
| pubmed:author | |
| pubmed:issnType |
Electronic
|
| pubmed:day |
26
|
| pubmed:volume |
16
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
8466-70
|
| pubmed:meshHeading |
pubmed-meshheading:20544751-Amino Acids, Aromatic,
pubmed-meshheading:20544751-Light,
pubmed-meshheading:20544751-Magnetic Resonance Spectroscopy,
pubmed-meshheading:20544751-Molecular Structure,
pubmed-meshheading:20544751-Organometallic Compounds,
pubmed-meshheading:20544751-Peptides,
pubmed-meshheading:20544751-Ruthenium,
pubmed-meshheading:20544751-Stereoisomerism
|
| pubmed:year |
2010
|
| pubmed:articleTitle |
Simple synthesis of ruthenium pi complexes of aromatic amino acids and small peptides.
|
| pubmed:affiliation |
A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 119991 Moscow, Russian Federation.
|
| pubmed:publicationType |
Journal Article
|