2003
Polycyclic ferrocenyl-4,5-dihydropyrazoles in nucleophilic reactions with beta-dicarbonyl compounds Elena I. Klimova, Tatiana Klimova, Marcos Martínez García, Eduardo A. Vázquez López, Rafael Moreno Esparza, José G. Alvarado Rodríguez, Teresa Ramírez Apan Journal of Organometallic Chemistry (2003), 665, 69-75. http://dx.doi.org/10.1016/S0022-328X(02)02064-8
Abstract
Polycyclic ferrocenyldihydropyrazoles with a free ?NH group react with ethyl acetoacetate and acetylacetone to give the corresponding enamino carbonyl compounds isolated as E-isomers. The spatial structure of (E)-4-[1-(ethoxycarbonyl)prop-2-en-2-yl]-3-ferrocenyl-1,4,5-triazatricyclo[5.2.2.02,6]undec-5-ene was determined using X-ray diffraction analysis. Spontaneous isomerization of (E)-(4-oxopent-2-en-2-yl)(ferrocenyl)dihydropyrazoles into the respective Z-isomers was observed.
Structural Studies by NMR and X-Ray Crystallography of N-(p-Toluenesulfonyl)-Amino Acids
Pyrite?Arsenopyrite Galvanic Interaction and Electrochemical Reactivity
Mild Oxidation of C?C Bonds of Benzoiridacycles
Study on the intramolecular transannular chalcogentin interactions in dithiastannecine compounds.