Giovanni Desimoni - Concepedia

Author

Giovanni Desimoni

University of Pavia

Also Known As

Desimoni, G., G. DESIMONI, G. Desimoni, GIOVANNI DESIMONI, Giovanni Desimoni

193

Publications

4.5K

Citations

H-Index

Concepts

All Affiliations

University of Pavia

About

Giovanni Desimoni is an author at University of Pavia specializing in chemistry, organic chemistry, and engineering.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	25	46	1.5K
2	Chemical Engineering	16	20	695
3	Biomolecular Engineering	15	19	647
4	Natural Sciences	11	13	382
5	Biochemistry	7	7	139

Giovanni Desimoni

Publications

2.1K

Citations

H-Index

Page 1

	Year	Citations
A new and highly efficient catalyst for the enantioselective Mukaiyama–Michael reaction between ( E )-3-crotonoyl-1,3-oxazolidin-2-one and 2-trimethylsilyloxyfuran Giovanni Desimoni, Giuseppe Faita, Salvatore Filippone, Tetrahedron Chemical EngineeringEngineeringOrganic ChemistryOrganometallic CatalysisCatalysis	2001	102
Asymmetric Friedel–Crafts Alkylation of Indoles with Methyl (<i>E</i>)‐2‐Oxo‐4‐aryl‐3‐butenoates Catalyzed by Sc(OTf)<sub>3</sub>/pybox Giovanni Desimoni, Giuseppe Faita, Marco Toscanini, Chemistry - A European Journal Enantioselective SynthesisDerivativesAsymmetric Friedel–crafts AlkylationEngineeringNatural Sciences	2008	69
The first enantioselective synthesis of both Diels-Alder enantiomers with the same bis(oxazoline)-magnesium perchlorate chiral catalyst Giovanni Desimoni, Giuseppe Faita, P. P. RIGHETTI Tetrahedron Letters Diels-alder EnantiomersSame BisOrganic ChemistryStereoselective SynthesisChemistry	1996	67
Solvent effect as the result of frontier molecular orbital interaction. V. Diels-Alder with heterodienophiles: a unified approach to the solvent effect of the Diels-Alder reactions Giovanni Desimoni, Giuseppe Faita, P. P. RIGHETTI, Tetrahedron Cross-coupling ReactionEngineeringAlkene MetathesisV. Diels-alderSolvent Effect	1990	65
Can a chiral catalyst containing the same ligand/metal components promote the formation of both enantiomers enantioselectively? The bis(oxazoline)-magnesium perchlorate-catalyzed asymmetric Diels-Alder reaction Giovanni Desimoni, Giuseppe Faita, Anna Gamba Invernizzi, Tetrahedron EngineeringOrganic ChemistryOrganometallic CatalysisCatalysisSame Ligand/metal Components	1997	63
A New Pyridine‐2,6‐bis(oxazoline) for Efficient and Flexible Lanthanide‐Based Catalysts of Enantioselective Reactions with 3‐Alkenoyl‐2‐oxazolidinones Giovanni Desimoni, Giuseppe Faita, Matilde Guala, Chemistry - A European Journal Enantioselective ReactionsChemical EngineeringEngineeringHeterocyclicOpposite Enantiomers	2005	61
Chiral amplification in Diels-Alder and 1,3-dipolar cycloadditions catalyzed by bis(oxazoline)-Zn(II)-based chiral complexes Stefano Crosignani, Giovanni Desimoni, Giuseppe Faita, Tetrahedron Letters EngineeringChiral AmplificationHeterocyclic1,3-Dipolar CycloadditionsOrganic Chemistry	1999	60
Copper(II) in organic synthesis. VIII enantioselective michael reactions with chiral copper(II) complexes as catalysts Giovanni Desimoni, Paolo Quadrelli, P. P. RIGHETTI Tetrahedron Chiral CopperChemical EngineeringEngineeringOrganic ChemistryOrganometallic Catalysis	1990	59
Copper (II) in organic synthesis. XI. Evaluation of the ligand architecture on the efficiency of a copper (II) catalyst for enantioselective Michael reactions Giovanni Desimoni, Guglielmo Dusi, Giuseppe Faita, Tetrahedron Ligand ArchitectureChemical EngineeringEngineeringOrganic ChemistryOrganometallic Catalysis	1995	58
Chiral Lewis acid controlled Diels-Alder reaction: Factors affecting the stereoselective formation of both enantiomers in the bis(oxazoline)-magnesium catalyzed process Paolo Carbone, Giovanni Desimoni, Giuseppe Faita, Tetrahedron Chiral Lewis AcidEngineeringStereoselective FormationOrganic ChemistryCatalysis	1998	54

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