The cytotoxic effect of Ru(II) complexes with 5-(2-hydroxyphenyl)-3-methyl-1-(2-pyridyl)-1H-pyrazole-4-carboxylic acid methyl ester: Synthesis, X-ray structure and DNA damage potential

Polyhedron ◽  
2019 ◽  
Vol 169 ◽  
pp. 228-238 ◽  
Author(s):  
Anna Skoczyńska ◽  
Beata Pasternak ◽  
Magdalena Małecka ◽  
Urszula Krajewska ◽  
Marek Mirowski ◽  
...  
1982 ◽  
Vol 60 (16) ◽  
pp. 2062-2064
Author(s):  
George M. Strunz ◽  
Peter S. White

The relative configurations of two intermediates in the synthetic route to cryptosporiopsin are clarified through the structure of 3,5-dichloro-1,4-dihydroxy-2-methylcyclopent-2-ene-1-carboxylic acid methyl ester, which was determined by single crystal X-ray techniques. The crystal was monoclinic, space group P21/c, a = 7.352(1), b = 8.868 (3), c = 16.300(7) Å; β = 96.49(2)°. The structure was solved by direct methods and refined to a final R of 0.057.


2007 ◽  
Vol 52 (2) ◽  
pp. 580-585 ◽  
Author(s):  
Maria D. M. C. Ribeiro da Silva ◽  
Vera L. S. Freitas ◽  
Luís M. N. B. F. Santos ◽  
Michal Fulem ◽  
M. J. Sottomayor ◽  
...  

1997 ◽  
Vol 40 (24) ◽  
pp. 3861-3864 ◽  
Author(s):  
Bruce E. Blough ◽  
Philip Abraham ◽  
Andrew C. Mills ◽  
Anita H. Lewin ◽  
John W. Boja ◽  
...  

Evergreen ◽  
2020 ◽  
Vol 7 (2) ◽  
pp. 275-279
Author(s):  
Shafira Nabilla ◽  
Sesia Fitri Anisa ◽  
Kania Zara ◽  
Setijo Bismo

1983 ◽  
Vol 38 (2) ◽  
pp. 220-225 ◽  
Author(s):  
W. S. Sheldrick ◽  
W. Trowitzsch

Abstract X-ray structural analyses of two α,γ-diketo esters and one α,γ-diketo acid, which are amino acid antagonists, have shown them all to be present in the solid state in the α,β-unsaturated γ-keto enolic form. The structures of the esters β-acetyl-pyruvic acid methyl ester (1) and 2-oxo-cyclopentyl-glyoxylic acid ethyl ester (3) are stabilized by intra-molecular O···H(-O) hydrogen bonds involving the enol proton. In the case of camphor oxalic acid (4) an intramolecular O···H-O hydrogen bond between the γ-keto oxygen and the acid proton is observed. The bond lengths and angles in 1 indicate a significant contribution from the mesomeric β,γ-unsaturated enol form. For comparison purposes the structure of the γ-enol methyl ether of 1, (4-methoxy-2-oxo-pentene)carboxylic acid methyl ester (2) has also been determined. The X-ray structures of the cyclization products of respectively an α,γ-diketo acid and an α,γ-diketo ester are reported.


1996 ◽  
Vol 47 (1) ◽  
pp. 79-81 ◽  
Author(s):  
John L. Musachio ◽  
Kathryn I. Keverline ◽  
F.Ivy Carroll ◽  
Robert F. Dannals

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