Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Nina Dovalil"'
Publikováno v:
Inorganic Chemistry. 50:5165-5174
The synthesis and Cu(II) coordination chemistry of the cyclic pseudo-octapeptide H(4)pat(1), a dimethyl-imidazole analogue of naturally occurring cyclic peptides (patellamide A-F, ascidiacyclamide) is reported. Substitution of the oxazoline and thiaz
Autor:
Jong Seung Kim, Young Ho Lee, Peter Comba, Hyang Hoo Kim, Marta Zajaczkowski, Nina Dovalil, Yang Kim, Pierre Thuéry
Publikováno v:
Journal of Inclusion Phenomena and Macrocyclic Chemistry. 65:59-64
Reported are the crystal and solution structures (determined by X-ray crystallography and EPR spectroscopy/simulation of the EPR spectra, respectively) of two dinuclear CuII complexes, coordinated to isomeric dinucleating azetidine-based ligands, who
Autor:
Jeffrey Harmer, Christopher J. Noble, Peter Comba, Nina Dovalil, Graeme R. Hanson, Bjoern Seibold, Mark J. Riley
Publikováno v:
Inorganic chemistry. 53(23)
Three synthetic analogues of westiallamide, H3L(wa), have previously been synthesized (H3L(1-3)) that have a common backbone (derived from l-valine) with H3L(wa) but differ in their heterocyclic rings (imidazole, oxazole, thiazole, and oxazoline). He
Publikováno v:
Dalton transactions (Cambridge, England : 2003). 43(5)
Cyclic pseudo-peptides derived from marine metabolites of the genus Lissoclinum bistratum and Lissoclinum patella have attracted scientific interest in the last two decades. Their structural properties and solution dynamics have been analyzed in deta
Publikováno v:
Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry. 15(7)
The CuII coordination chemistry of three synthetic analogues of westiellamide (H3Lwa) with an [18]azacrown-6 macrocyclic structure and imidazole (H3L1), oxazole (H3L2), or thiazole (H3L3) heterocyclic donors in addition to the peptide groups, is repo