The scientist’s investigation covers issues in Organic chemistry, Catalysis, Palladium, Medicinal chemistry and Aryl. His study in the field of Annulation, Reagent, Nucleophile and Ammonia is also linked to topics like Environmentally friendly. In general Catalysis, his work in Regioselectivity, Tributylamine and Norbornadiene is often linked to Norbornene linking many areas of study.
His Palladium research integrates issues from Yield, Halide, Carbonylation, Transition state and Bicyclic molecule. While the research belongs to areas of Medicinal chemistry, Fabio Marinelli spends his time largely on the problem of Alkylation, intersecting his research to questions surrounding Indole test, Dibenzylidene acetone and Organic reaction. His study in Aryl is interdisciplinary in nature, drawing from both Potassium carbonate, Carboxylic acid, Lactone and Phosphine.
His primary areas of study are Catalysis, Organic chemistry, Palladium, Medicinal chemistry and Aryl. His studies examine the connections between Catalysis and genetics, as well as such issues in Alkyl, with regards to Formate. The Palladium study combines topics in areas such as Yield, Polymer chemistry, Halide, Carbonylation and Stereoselectivity.
His Trimethylsilyl study in the realm of Medicinal chemistry interacts with subjects such as Triple bond, Conjugate and Reduction. His Aryl research incorporates elements of Allylic rearrangement, Stereochemistry and α methylene γ butyrolactone. His Annulation study which covers Amination that intersects with Propynyl.
Fabio Marinelli focuses on Catalysis, Organic chemistry, Medicinal chemistry, Combinatorial chemistry and Aryl. In the field of Catalysis, his study on Palladium, Oxidative cyclization and Alkyne overlaps with subjects such as Cascade. As part of the same scientific family, Fabio Marinelli usually focuses on Palladium, concentrating on Oxidative phosphorylation and intersecting with Acetanilide.
His Organic chemistry study often links to related topics such as Oxidation reduction. The study incorporates disciplines such as Intramolecular force and Brønsted–Lowry acid–base theory in addition to Medicinal chemistry. The concepts of his Aryl study are interwoven with issues in Cascade reaction and Stereoselectivity.
His primary scientific interests are in Catalysis, Organic chemistry, Combinatorial chemistry, Aryl and Cascade reaction. His research in Catalysis intersects with topics in Intramolecular force, Medicinal chemistry and Intermolecular force. His work carried out in the field of Medicinal chemistry brings together such families of science as Acyl group and Copper.
His Organic chemistry study frequently intersects with other fields, such as Oxidation reduction. The various areas that Fabio Marinelli examines in his Combinatorial chemistry study include Indole test and Lone pair. He merges Aryl with Cascade in his study.
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Palladium-Catalyzed Reaction of o-Ethynylphenols, o-((Trimethylsilyl)ethynyl)phenyl Acetates, and o-Alkynylphenols with Unsaturated Triflates or Halides: A Route to 2-Substituted-, 2,3-Disubstituted-, and 2-Substituted-3-acylbenzo[b]furans
Antonio Arcadi;Sandro Cacchi;Mario Del Rosario;and Giancarlo Fabrizi.
Journal of Organic Chemistry (1996)
Palladium-catalysed coupling of aryl and vinyl triflates or halides with 2-ethynylaniline: An efficient route to functionalized 2-substituted indoles
A. Arcadi;S. Cacchi;F. Marinelli.
Tetrahedron Letters (1989)
Gold catalysis in the reactions of 1,3-dicarbonyls with nucleophiles
A. Arcadi;G. Bianchi;S. Di Giuseppe;F. Marinelli.
Green Chemistry (2003)
Gold-Catalyzed Reactions of 2-Alkynyl-phenylamines with α,β-Enones
Maria Alfonsi;Antonio Arcadi;Massimiliano Aschi;Gabriele Bianchi.
Journal of Organic Chemistry (2005)
Sequential Amination/Annulation/Aromatization Reaction of Carbonyl Compounds and Propargylamine: A New One-Pot Approach to Functionalized Pyridines
Giorgio Abbiati;Antonio Arcadi;Gabriele Bianchi;Sabrina Di Giuseppe.
Journal of Organic Chemistry (2003)
Electrophilic cyclization of o-acetoxy- and o-benzyloxyalkynylpyridines: an easy entry into 2,3-disubstituted furopyridines.
Arcadi A;Cacchi S;Di Giuseppe S;Fabrizi G.
Organic Letters (2002)
Preparation of 2,5-disubstituted oxazoles from N-propargylamides.
Antonio Arcadi;Sandro Cacchi;Lauro Cascia;Giancarlo Fabrizi.
Organic Letters (2001)
Gold(III)-Catalyzed Annulation of 2-Alkynylanilines: A Mild and Efficient Synthesis of Indoles and 3-Haloindoles
Antonio Arcadi;Gabriele Bianchi;Fabio Marinelli.
2-Substituted-3-acylindoles through the Palladium-Catalysed Carbonylative Cyclization of 2-Alkynyltrifluoroacetanilides with Aryl Halides and Vinyl Triflates
Antonio Arcadi;Sandro Cacchi;Veronica Carnicelli;Fabio Marinelli.
A New Approach to 2,3-Disubstituted Benzo[b]furans from o-Alkynylphenols via 5-endo-dig-Iodocyclisation/Palladium-Catalysed Reactions
Antonio Arcadi;Sandro Cacchi;Giancarlo Fabrizi;Fabio Marinelli.
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