Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Marisa Belicchi Ferrari"'
Autor:
Enrico Buluggiu, Giorgio Pelosi, Marisa Belicchi-Ferrari, Franco Bisceglie, Pieralberto Tarasconi
Publikováno v:
Polyhedron. 29:2134-2141
The syntheses of four compounds, obtained by the reaction of methylpyruvate thiosemicarbazone (Hmpt) and its methyl (Me-Hmpt) and allyl (Allyl-Hmpt) derivatives with bis(triphenylphosphine)copper(I) acetate, are reported. The compounds [Cu(PPh3)2(ptc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce888f1939af1d6090a5efcb42b0b794
https://doi.org/10.1016/j.poly.2010.04.009
https://doi.org/10.1016/j.poly.2010.04.009
Autor:
Marco Giannetto, Federica Giordani, Annamaria Buschini, Marisa Belicchi Ferrari, Silvana Pinelli, Franco Bisceglie, Claudia Pellacani, Pieralberto Tarasconi, Giorgio Pelosi
Publikováno v:
Journal of Inorganic Biochemistry. 103:666-677
Thiosemicarbazones are versatile organic compounds that present considerable pharmaceutical interest because of a wide range of properties. In our laboratory we synthesised some new metal-complexes with thiosemicarbazones derived from natural aldehyd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0f9fb9d1ac6c96897ae7f9c5c58fa6c
https://doi.org/10.1016/j.jinorgbio.2008.12.016
https://doi.org/10.1016/j.jinorgbio.2008.12.016
Autor:
Marisa Belicchi-Ferrari, Franco Bisceglie, Giorgio Pelosi, Pieralberto Tarasconi, Enrico Buluggiu
Publikováno v:
Polyhedron. 28:1160-1168
This paper reports the synthesis of a series of methylpyruvate thiosemicarbazone derivatives containing, on the terminal nitrogen, substituents of different nature and size and namely, ethyl, phenyl and methylphenyl. These ligands were reacted with b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b27a48bac16974067143ff3cf5f9fc8
https://doi.org/10.1016/j.poly.2009.01.013
https://doi.org/10.1016/j.poly.2009.01.013
Publikováno v:
Polyhedron. 27:1361-1367
By reacting thiosemicarbazides substituted on the aminic nitrogen with 5-formyluracil, several new 5-formyluracil thiosemicarbazones (H 3 ut) derivatives were synthesised and characterized. These ligands, treated with copper chloride and nitrate, aff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5aabf9dc69d7f27f8e7185f3e99d0dfb
https://doi.org/10.1016/j.poly.2007.12.034
https://doi.org/10.1016/j.poly.2007.12.034
Autor:
Pieralberto Tarasconi, Silvana Pinelli, Franco Bisceglie, Giorgio Pelosi, Marisa Belicchi-Ferrari
Publikováno v:
Polyhedron. 26:5150-5161
In the course of a research on metal-based compounds active on white blood cell cancers (leukemia, lymphoma and myeloma) nine aliphatic thiosemicarbazones and their nickel complexes have been synthesized with the aim to test their effect on histiocyt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::839944f2d06da32969ffde41318151cd
https://doi.org/10.1016/j.poly.2007.07.014
https://doi.org/10.1016/j.poly.2007.07.014
Autor:
Giorgio Pelosi, Chiara Cavalieri, Marisa Belicchi-Ferrari, Pieralberto Tarasconi, Franco Bisceglie
Publikováno v:
Polyhedron. 26:3774-3782
This paper reports the synthesis and characterization of six compounds of copper(I), stabilized in its reduced state by two triphenylphosphines, in which 4-fluorobenzaldehyde thiosemicarbazone and N-methylthiosemicarbazone act as chelating through th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ec1aaabd79a9c4256a1a24a5db60efc
https://doi.org/10.1016/j.poly.2007.04.026
https://doi.org/10.1016/j.poly.2007.04.026
Autor:
Pieralberto Tarasconi, Enrico Cavalli, Franco Bisceglie, Vincenzo Verdolino, Marisa Belicchi Ferrari, Giorgio Pelosi
Publikováno v:
Inorganica Chimica Acta. 360:3233-3240
Reaction of phenylisothiocyanate with different aromatic amines allowed the synthesis of compounds containing the thiourea moiety. By reacting silver bis(triphenylphosphine)nitrate with suitable ligands belonging to this family of sulphurated compoun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a8bd849cbbad22a9433091ceed0a6d8b
https://doi.org/10.1016/j.ica.2007.03.025
https://doi.org/10.1016/j.ica.2007.03.025
Publikováno v:
Inorganica Chimica Acta. 360:2814-2818
The 2:1 reaction of [Ru(H2O)2(NH3)5]2+ with 1,2,4,5-tetrazine (tz) gives rise to the formation of the dinuclear complex ion [{Ru(NH3)5}2(μ-tz-N1:N4)]4+. Its tetraphenylborate and hexafluoro-phosphate salts have been fully characterized; the X-ray st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b264538ec02de973f1f2ad156ba6262d
https://doi.org/10.1016/j.ica.2006.12.044
https://doi.org/10.1016/j.ica.2006.12.044
Autor:
Silvana Pinelli, Marisa Belicchi-Ferrari, Maria Careri, Franco Bisceglie, Pieralberto Tarasconi, Enrico Buluggiu, Giorgio Pelosi, Monica Baldini
Publikováno v:
European Journal of Medicinal Chemistry. 42:627-634
9-cis-Retinal thiosemicarbazone and its Co(III), Ni(II) and Cu(II) complexes are synthesized and characterized. Central Co(III) atom is in an octahedral environment while Ni(II) and Cu(II) atoms are in a square planar environment. DNA binding constan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4da8a6a2a4a3e164766926028e295c5e
https://doi.org/10.1016/j.ejmech.2006.12.019
https://doi.org/10.1016/j.ejmech.2006.12.019
Autor:
Giorgio Pelosi, Silvana Pinelli, Monica Sassi, María C. Rodríguez-Argüelles, Corrado Pelizzi, Marisa Belicchi Ferrari, Franco Bisceglie
Publikováno v:
Journal of Inorganic Biochemistry. 98:313-321
Nickel, copper, and zinc complexes of isatin (H(2)L(1)) and N-methylisatin 3-picolinoyl hydrazone (HL(2)), were synthesized and characterized by means of spectroscopic techniques. H(2)L(1) and a nickel complex [Ni(L(2))(2)].2C(6)H(14) were also chara
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b570e3d03639c314b8c9087f0dac7906
https://doi.org/10.1016/j.jinorgbio.2003.10.006
https://doi.org/10.1016/j.jinorgbio.2003.10.006