-transparent.png){kind=logo}
Simple synthesis of ruthenium pi complexes of aromatic amino acids and small peptides. 2010
Dmitry S Perekalin, and
Eduard E Karslyan, and
Pavel V Petrovskii, and
Yulia V Nelyubina, and
Konstantin A Lyssenko, and
Alexey S Kononikhin, and
Eugene N Nikolaev, and
Alexander R Kudinov
A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 119991 Moscow, Russian Federation.
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.
Related Publications
Dmitry S Perekalin, and
Eduard E Karslyan, and
Pavel V Petrovskii, and
Yulia V Nelyubina, and
Konstantin A Lyssenko, and
Alexey S Kononikhin, and
Eugene N Nikolaev, and
Alexander R Kudinov
June 2007,
The Journal of nutrition,
Dmitry S Perekalin, and
Eduard E Karslyan, and
Pavel V Petrovskii, and
Yulia V Nelyubina, and
Konstantin A Lyssenko, and
Alexey S Kononikhin, and
Eugene N Nikolaev, and
Alexander R Kudinov
July 2001,
Inorganic chemistry,
Dmitry S Perekalin, and
Eduard E Karslyan, and
Pavel V Petrovskii, and
Yulia V Nelyubina, and
Konstantin A Lyssenko, and
Alexey S Kononikhin, and
Eugene N Nikolaev, and
Alexander R Kudinov
January 2007,
Dalton transactions (Cambridge, England : 2003),
Dmitry S Perekalin, and
Eduard E Karslyan, and
Pavel V Petrovskii, and
Yulia V Nelyubina, and
Konstantin A Lyssenko, and
Alexey S Kononikhin, and
Eugene N Nikolaev, and
Alexander R Kudinov
January 2013,
Metal ions in life sciences,
Dmitry S Perekalin, and
Eduard E Karslyan, and
Pavel V Petrovskii, and
Yulia V Nelyubina, and
Konstantin A Lyssenko, and
Alexey S Kononikhin, and
Eugene N Nikolaev, and
Alexander R Kudinov
March 2018,
Tetrahedron letters,
Dmitry S Perekalin, and
Eduard E Karslyan, and
Pavel V Petrovskii, and
Yulia V Nelyubina, and
Konstantin A Lyssenko, and
Alexey S Kononikhin, and
Eugene N Nikolaev, and
Alexander R Kudinov
September 2009,
Journal of the American Chemical Society,
Dmitry S Perekalin, and
Eduard E Karslyan, and
Pavel V Petrovskii, and
Yulia V Nelyubina, and
Konstantin A Lyssenko, and
Alexey S Kononikhin, and
Eugene N Nikolaev, and
Alexander R Kudinov
February 2024,
Angewandte Chemie (International ed. in English),
Dmitry S Perekalin, and
Eduard E Karslyan, and
Pavel V Petrovskii, and
Yulia V Nelyubina, and
Konstantin A Lyssenko, and
Alexey S Kononikhin, and
Eugene N Nikolaev, and
Alexander R Kudinov
April 1967,
Biochimica et biophysica acta,
Dmitry S Perekalin, and
Eduard E Karslyan, and
Pavel V Petrovskii, and
Yulia V Nelyubina, and
Konstantin A Lyssenko, and
Alexey S Kononikhin, and
Eugene N Nikolaev, and
Alexander R Kudinov
July 2014,
Angewandte Chemie (International ed. in English),
Dmitry S Perekalin, and
Eduard E Karslyan, and
Pavel V Petrovskii, and
Yulia V Nelyubina, and
Konstantin A Lyssenko, and
Alexey S Kononikhin, and
Eugene N Nikolaev, and
Alexander R Kudinov
November 1977,
Journal of medicinal chemistry,
