Organic chemistry, Enantioselective synthesis, Organocatalysis, Catalysis and Stereochemistry are his primary areas of study. His studies in Michael reaction, Alkylation, Indole test, Bartoli indole synthesis and Ketone are all subfields of Organic chemistry research. His Enantioselective synthesis research integrates issues from Halogenation, Cyclopropanation and Amine gas treating.
His Organocatalysis study combines topics from a wide range of disciplines, such as Aldehyde, Quaternary carbon, Molecule, Cascade reaction and Electrophilic substitution. His study in Catalysis is interdisciplinary in nature, drawing from both Combinatorial chemistry and Maleimide. The Stereochemistry study which covers Stereocenter that intersects with Chirality and Bifunctional.
Giuseppe Bartoli mostly deals with Organic chemistry, Reagent, Medicinal chemistry, Catalysis and Alkyl. Enantioselective synthesis, Lewis acids and bases, Organocatalysis, Alkylation and Cerium are subfields of Organic chemistry in which his conducts study. Iminium is closely connected to Amine gas treating in his research, which is encompassed under the umbrella topic of Enantioselective synthesis.
His Reagent research is multidisciplinary, incorporating elements of Combinatorial chemistry, Yield, Addition reaction and Chemoselectivity. His Medicinal chemistry course of study focuses on Reactivity and Nucleophile. The Alkyl study combines topics in areas such as Stereochemistry and Stereoselectivity.
The scientist’s investigation covers issues in Organic chemistry, Organocatalysis, Enantioselective synthesis, Catalysis and Combinatorial chemistry. In his works, Giuseppe Bartoli conducts interdisciplinary research on Organic chemistry and Hydrophosphination. Giuseppe Bartoli combines subjects such as Mannich reaction, Stereochemistry and Aldehyde with his study of Organocatalysis.
His research integrates issues of Alkylation, Cyclopropanation, Michael reaction, Nucleophile and Amine gas treating in his study of Enantioselective synthesis. In general Catalysis study, his work on Stereocenter, Stereoselectivity and Aldol reaction often relates to the realm of Glyoxylate cycle, thereby connecting several areas of interest. His Combinatorial chemistry research incorporates themes from Cascade reaction and Molecule.
His scientific interests lie mostly in Organic chemistry, Enantioselective synthesis, Organocatalysis, Catalysis and Stereochemistry. His Organic chemistry study frequently links to related topics such as Environmental chemistry. His Enantioselective synthesis study combines topics in areas such as Bifunctional, Cyclopropanation, Michael reaction and Amine gas treating.
The study incorporates disciplines such as Selectivity, Reactivity, Nucleophile and Iminium in addition to Amine gas treating. The various areas that Giuseppe Bartoli examines in his Organocatalysis study include Ketone, Cascade reaction, Molecule and Aldehyde. His work in the fields of Catalysis, such as Dicarbonate, intersects with other areas such as Acetoxy group.
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Asymmetric aminocatalysis--gold rush in organic chemistry.
Paolo Melchiorre;Mauro Marigo;Armando Carlone;Giuseppe Bartoli.
Angewandte Chemie (2008)
Recent advances in organocatalytic methods for the synthesis of disubstituted 2- and 3-indolinones
Renato Dalpozzo;Giuseppe Bartoli;Giorgio Bencivenni.
Chemical Society Reviews (2012)
Targeting Structural and Stereochemical Complexity by Organocascade Catalysis: Construction of Spirocyclic Oxindoles Having Multiple Stereocenters
Giorgio Bencivenni;Li-Yuan Wu;Andrea Mazzanti;Berardino Giannichi.
Angewandte Chemie (2009)
Organocatalytic strategies for the asymmetric functionalization of indoles
Giuseppe Bartoli;Giorgio Bencivenni;Renato Dalpozzo.
Chemical Society Reviews (2010)
Die asymmetrische Aminokatalyse – Goldrausch in der organischen Chemie
Paolo Melchiorre;Mauro Marigo;Armando Carlone;Giuseppe Bartoli.
Angewandte Chemie (2008)
The reaction of vinyl grignard reagents with 2-substituted nitroarenes: A new approach to the synthesis of 7-substituted indoles
Giuseppe Bartoli;Gianni Palmieri;Marcella Bosco;Renato Dalpozzo.
Tetrahedron Letters (1989)
Organocatalytic Asymmetric Friedel−Crafts Alkylation of Indoles with Simple α,β-Unsaturated Ketones
Giuseppe Bartoli;Marcella Bosco;Armando Carlone;Fabio Pesciaioli.
Organic Letters (2007)
Chemo- and Diastereoselective Reduction of .beta.-Enamino Esters: A Convenient Synthesis of Both cis- and trans-.gamma.-Amino Alcohols and .beta.-Amino Esters
Giuseppe Bartoli;Cristina Cimarelli;Enrico Marcantoni;Gianni Palmieri.
Journal of Organic Chemistry (1994)
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)
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