Letizia Sambri spends much of her time researching Organic chemistry, Enantioselective synthesis, Organocatalysis, Catalysis and Sodium iodide. Her Organic chemistry study frequently draws parallels with other fields, such as Environmental chemistry. Her studies deal with areas such as Bifunctional, Iminium, Stereochemistry and Amine gas treating as well as Enantioselective synthesis.
Her Organocatalysis research includes elements of Halogenation, Aldehyde and Electrophilic substitution. The concepts of her Catalysis study are interwoven with issues in Maleimide and Perchloric acid. Her Sodium iodide research is multidisciplinary, incorporating elements of Nuclear chemistry, Inorganic chemistry, Stereospecificity and Cerium chloride, Chloride.
The scientist’s investigation covers issues in Organic chemistry, Catalysis, Reagent, Alkyl and Lewis acids and bases. Her Enantioselective synthesis, Reactivity, Sodium iodide and Alcohol study, which is part of a larger body of work in Organic chemistry, is frequently linked to Magnesium perchlorate, bridging the gap between disciplines. Her Enantioselective synthesis study deals with Amine gas treating intersecting with Selectivity and Iminium.
Her Catalysis study combines topics from a wide range of disciplines, such as Combinatorial chemistry and Primary. As part of the same scientific family, Letizia Sambri usually focuses on Reagent, concentrating on Cerium and intersecting with Chloride. Her Alkyl research includes themes of Titanium, Stereochemistry, Medicinal chemistry and Stereoselectivity.
Her primary scientific interests are in Iridium, Photochemistry, Catalysis, Combinatorial chemistry and Photocatalysis. Letizia Sambri has researched Iridium in several fields, including Polymeric nanoparticles, Luminescence, Ligand and Cationic polymerization, Polymer chemistry. Her Catalysis study introduces a deeper knowledge of Organic chemistry.
Letizia Sambri interconnects Hydrolysis, Carbamate and Aqueous solution in the investigation of issues within Combinatorial chemistry. Her Photocatalysis study combines topics in areas such as Electrophile, Alkylation, Zinc, Michael reaction and Cyclam. Letizia Sambri has included themes like Alkyl radicals and Medicinal chemistry in her Zinc study.
Letizia Sambri focuses on Iridium, Catalysis, Cationic polymerization, Ligand and Pyridine. Her Catalysis study is related to the wider topic of Organic chemistry. Her research is interdisciplinary, bridging the disciplines of Medicinal chemistry and Organic chemistry.
Her Cationic polymerization study incorporates themes from Photochemistry, HOMO/LUMO, Mesoionic and Density functional theory. Her work is dedicated to discovering how Density functional theory, Acetonitrile are connected with Combinatorial chemistry and other disciplines. Letizia Sambri works mostly in the field of Pyridine, limiting it down to topics relating to Hydrogen transfer and, in certain cases, Carbene, as a part of the same area of interest.
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Organocatalytic Asymmetric Friedel−Crafts Alkylation of Indoles with Simple α,β-Unsaturated Ketones
Giuseppe Bartoli;Marcella Bosco;Armando Carlone;Fabio Pesciaioli.
Organic Letters (2007)
Conjugate Addition of Amines to α,β-Enones Promoted by CeCl3·7H2O−NaI System Supported in Silica Gel
Giuseppe Bartoli;Marcella Bosco;Enrico Marcantoni;Marino Petrini.
Journal of Organic Chemistry (2001)
The Michael addition of indoles to alpha,beta-unsaturated ketones catalyzed by CeCl3.7H2O-NaI combination supported on silica gel.
Giuseppe Bartoli;Massimo Bartolacci;Marcella Bosco;Gioia Foglia.
Journal of Organic Chemistry (2003)
Organocatalytic Asymmetric Conjugate Addition of 1,3‐Dicarbonyl Compounds to Maleimides
Giuseppe Bartoli;Marcella Bosco;Armando Carlone;Andrea Cavalli.
Angewandte Chemie (2006)
Asymmetric Iminium Ion Catalysis with a Novel Bifunctional Primary Amine Thiourea: Controlling Adjacent Quaternary and Tertiary Stereocenters
Patrizia Galzerano;Giorgio Bencivenni;Fabio Pesciaioli;Andrea Mazzanti.
Chemistry: A European Journal (2009)
Organocatalytic Asymmetric Sulfa-Michael Addition to α,β-Unsaturated Ketones
Paolo Ricci;Armando Carlone;Giuseppe Bartoli;Marcella Bosco.
Advanced Synthesis & Catalysis (2008)
Organocatalytic asymmetric hydrophosphination of α, β-unsaturated aldehydes
Armando Carlone;Giuseppe Bartoli;Marcella Bosco;Letizia Sambri.
Angewandte Chemie (2007)
Cerium (III) Chloride, a Novel Reagent for Nonaqueous Selective Conversion of Dioxolanes to Carbonyl Compounds
Enrico Marcantoni;Francesco Nobili;Giuseppe Bartoli;Marcella Bosco.
Journal of Organic Chemistry (1997)
Asymmetric Aminolysis of Aromatic Epoxides: A Facile Catalytic Enantioselective Synthesis of anti-β-Amino Alcohols
Giuseppe Bartoli;Marcella Bosco;Armando Carlone;Manuela Locatelli.
Organic Letters (2004)
Efficient preparation of 2-indolyl-1-nitroalkane derivatives employing nitroalkenes as versatile Michael acceptors : New practical linear approach to alkyl 9H-β-carboline-4-carboxylate
Giuseppe Bartoli;Marcella Bosco;Sandra Giuli;Arianna Giuliani.
Journal of Organic Chemistry (2005)
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