Catalysis, Medicinal chemistry, Organic chemistry, Amination and Photochemistry are his primary areas of study. Sergio Cenini frequently studies issues relating to Phenanthroline and Catalysis. His biological study spans a wide range of topics, including Porphyrin, Nitrogen, Olefin fiber, Cyclopropanation and Reaction mechanism.
His work on Rhodium, Oxidative addition and Steric effects as part of general Organic chemistry study is frequently linked to Kinetic energy and Compound s, therefore connecting diverse disciplines of science. His work deals with themes such as Allylic rearrangement, Cyclohexene, Azide, Aryl and Nitrene, which intersect with Amination. His Photochemistry study combines topics in areas such as Transition metal and Homogeneous catalysis.
Sergio Cenini mainly focuses on Medicinal chemistry, Catalysis, Organic chemistry, Carbonylation and Ruthenium. His study in Medicinal chemistry is interdisciplinary in nature, drawing from both Inorganic chemistry, Reactivity, Carbon monoxide, Stereochemistry and Aryl. His Stereochemistry research focuses on subjects like Molecule, which are linked to Crystallography.
His research investigates the connection between Catalysis and topics such as Photochemistry that intersect with problems in Transition metal. Sergio Cenini has included themes like Rhodium and Nitro, Nitro compound in his Carbonylation study. His studies deal with areas such as Allylic rearrangement and Cyclohexene as well as Amination.
Sergio Cenini focuses on Catalysis, Organic chemistry, Ruthenium, Medicinal chemistry and Polymer chemistry. His studies in Catalysis integrate themes in fields like Combinatorial chemistry and Photochemistry. His Ruthenium study incorporates themes from Amination and Porphyrin.
His work carried out in the field of Medicinal chemistry brings together such families of science as Chemoselectivity, Nitrogen, Steric effects, Aryl and Reaction mechanism. He has researched Polymer chemistry in several fields, including Aniline, Membrane, Polymeric membrane and Nitrobenzene. In his research, Nitro and Monoxide is intimately related to Transition metal, which falls under the overarching field of Carbonylation.
The scientist’s investigation covers issues in Catalysis, Medicinal chemistry, Organic chemistry, Aryl and Photochemistry. Carbonylation, Alkyne, Palladium and Selectivity are the core of his Catalysis study. His Aryl research includes themes of Amination, Chemoselectivity, Porphyrin, Ruthenium and Nitrene.
The concepts of his Amination study are interwoven with issues in Combinatorial chemistry and Organic synthesis. His Nitrene study integrates concerns from other disciplines, such as Azide and Allylic rearrangement. His Photochemistry research incorporates themes from Organic reaction, Phenanthroline, Transition metal, Heteronuclear molecule and Coordination complex.
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Coordination chemistry of organic azides and amination reactions catalyzed by transition metal complexes
Sergio Cenini;Emma Gallo;Alessandro Caselli;Fabio Ragaini.
Coordination Chemistry Reviews (2006)
Amination of benzylic C-H bonds by arylazides catalyzed by CoII-porphyrin complexes: a synthetic and mechanistic study.
Fabio Ragaini;Andrea Penoni;Emma Gallo;Stefano Tollari.
Chemistry: A European Journal (2003)
Ruthenium carbonyl catalyzed reductive carbonylation of aromatic nitro compounds. A selective route to carbamates
Sergio Cenini;Corrado Crotti;Maddalena Pizzotti;Francesca Porta.
Journal of Organic Chemistry (1988)
Synthesis of Ar-BIAN Ligands (Ar-BIAN = Bis(aryl)acenaphthenequinonediimine) Having Strong Electron-Withdrawing Substituents on the Aryl Rings and Their Relative Coordination Strength toward Palladium(0) and -(II) Complexes
Michela Gasperini;Fabio Ragaini;Sergio Cenini.
Organometallics (2002)
Amination of benzylic C–H bonds by aryl azides catalysed by CoII(porphyrin) complexes. A new reaction leading to secondary amines and imines
Sergio Cenini;Emma Gallo;Andrea Penoni;Fabio Ragaini.
Chemical Communications (2000)
Synthesis, X-ray structure, and catalytic properties of the unprecedented tetranuclear copper(I) species [Cu(dppz)]4 (Hdppz = 3,5-diphenylpyrazole)
Ardizzoia Ga;Cenini S;Lamonica G;Masciocchi N.
Inorganic Chemistry (1994)
REACTION OF DIOXYGEN WITH [CU(DMPZ)]N (HDMPZ = 3,5-DIMETHYLPYRAZOLE) - CRYSTAL-STRUCTURE, REACTIVITY, AND CATALYTIC PROPERTIES OF [CU8(DMPZ)8(OH)8]
G Ardizzoia;M Angaroni;G Lamonica;F Cariati.
Inorganic Chemistry (1991)
Zerovalent platinum chemistry. Part VI. The reactions of bis- and tris-triphenylphosphineplatinum(0) with hydrogen sulphide, hydrogen selenide, sulphur, and related molecules
R. Ugo;G. La Monica;S. Cenini;A. Segre.
Journal of The Chemical Society A: Inorganic, Physical, Theoretical (1971)
Organic azides and isocyanates as sources of nitrene species in organometallic chemistry
S. Cenini;G. La Monica.
Inorganica Chimica Acta (1976)
The key intermediate in the amination of saturated C–H bonds: synthesis, X-ray characterization and catalytic activity of Ru(TPP)(NAr)2 (Ar = 3,5-(CF3)2C6H3)
Simone Fantauzzi;Emma Gallo;Alessandro Caselli;Fabio Ragaini.
Chemical Communications (2009)
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