Ludovico Ronzini - Concepedia

Author

Ludovico Ronzini

University of Bari Aldo Moro

Also Known As

L. RONZINI, L. Ronzini, LUDOVICO RONZINI, Ludovico Ronzini, Ronzini, L.

Publications

Citations

H-Index

Concepts

All Affiliations

University of Bari Aldo Moro University of Salento Institute of Molecular Science and Technologies Institute for the Chemistry of OrganoMetallic Compounds Istituto Nazionale di Fisica Nucleare, Sezione di Lecce

About

Ludovico Ronzini is an author at University of Bari Aldo Moro specializing in chemistry, organic chemistry, and engineering.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	14	17	661
2	Biomolecular Engineering	9	9	197
3	Natural Sciences	6	6	97
4	Biochemistry	4	4	50
5	Biology	1	1	34

Ludovico Ronzini

Publications

946

Citations

H-Index

Page 1

	Year	Citations
Iron catalyzed cross-coupling reactions of acyl chlorides with Grignard reagents. A mild, general, and convenient synthesis of aliphatic and aromatic ketones. Vito Fiandanese, Giuseppe Marchese, Virginia Martina, Tetrahedron Letters Chemical EngineeringCross-coupling ReactionEngineeringAromatic KetonesOrganic Chemistry	1984	123
A highly efficient synthetic route to ketones through sequential coupling reactions of grignard reagents with -phenyl carbonochloridothioate in the presence of nickel or iron catalysts Cosimo Cardellicchio, Vito Fiandanese, Giuseppe Marchese, Tetrahedron Letters Efficient Synthetic RouteChemical EngineeringCross-coupling ReactionEngineeringGrignard Reagents	1985	86
Functionalized ketones by iron mediated reaction of grignard reagents with acyl chlorides Cosimo Cardellicchio, Vito Fiandanese, Giuseppe Marchese, Tetrahedron Letters Chemical EngineeringEnantioselective SynthesisEngineeringGrignard ReagentsOrganic Chemistry	1987	76
One-step synthesis of ketones from car☐ylic acids and grignard reagents in the presence of a nickel(II)-phosphine catalyst. Vito Fiandanese, Giuseppe Marchese, Ludovico Ronzini Tetrahedron Letters Chemical EngineeringEngineeringGrignard ReagentsOrganometallic CatalysisOne-step Synthesis	1983	46
A stereospecific route to olefins through sequential coupling reaction of Grignard reagents with 1-bromo-2-phenylthioethene in the presence of nickel or palladium catalysts Vito Fiandanese, Giuseppe Marchese, Francesco Naso, Journal of the Chemical Society Chemical Communications Chemical EngineeringCross-coupling ReactionEngineeringAlkene MetathesisGrignard Reagents	1982	43
Stereospecific synthesis of (1E,3Z)- and (1E,3E)-1-trimethylsilyl-1,3- dienes by means of sequential cross-coupling reactions Vito Fiandanese, Giuseppe Marchese, G. Máscolo, Tetrahedron Letters Cross-coupling ReactionStereospecific Synthesis-1-Trimethylsilyl-1,3- DienesOrganic ChemistryStereoselective Synthesis	1988	42
Use of fluoride ion as a reagent in acetylene- and allene-forming eliminations Francesco Naso, Ludovico Ronzini Journal of the Chemical Society Perkin Transactions 1 HalogenationChemical EngineeringDerivative (Chemistry)DerivativesEngineering	1974	42
Stereoselective synthesis of heterosubstituted aziridines and their functionalization Luisella De Vitis, Saverio Florio, Catia Granito, Tetrahedron Organic ChemistryStereoselective SynthesisChemistryHeterocycle ChemistrySynthetic Chemistry	2003	36
Stereospecific synthesis of alkenyl sulphides by cross-coupling reactions of secondary alkyl Grignard reagents with Z- or E-1-bromo-2-phenylthioethene in the presence of transition metal catalysts Vito Fiandanese, Giovanni Miccoli, Francesco Naso, Journal of Organometallic Chemistry Asymmetric CatalysisChemical EngineeringCross-coupling ReactionEngineeringAlkene Metathesis	1986	35
Synthesis of 1,1-Disubstituted Ethenes by Means of Sequential Cross-Coupling Reactions Vito Fiandanese, Giuseppe Marchese, Francesco Naso, Synthesis Chemical EngineeringCross-coupling ReactionEngineeringAlkene MetathesisTransition-metal Catalysts	1987	34

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