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Achille Umani-Ronchi

Achille Umani-Ronchi

D-Index & Metrics

Chemistry

D-Index
50
Citations
9125
World Ranking
14364
National Ranking
491

Overview

Achille Umani-Ronchi is affiliated with the University of Bologna in Italy. Their academic profile reflects a career rooted at an institution with a significant history in higher education and research.

Currently, there is no available data on recent papers published by Achille Umani-Ronchi, so it is not possible to outline specific research outputs or highlight recent contributions to the field.

Similarly, there is no information regarding frequent co-authors or collaboration networks associated with their work, which would typically provide insight into research partnerships and scholarly communities.

No data is provided on frequent publication venues. Consequently, details about the typical journals, conferences, or other outlets where this researcher disseminates findings are not available.

Information about book publications is also unavailable, limiting the overview of their scholarly contributions to monographs or edited volumes.

There are no records concerning main fields of study, subfields, or specific research topics. This restricts the ability to define the thematic focus or specialized areas that characterize their scientific inquiry.

There are no awards listed for Achille Umani-Ronchi, so there are no recognitions or honors to report that might contextualize their standing in the academic community.

Best Publications

  • New Catalytic Approaches in the Stereoselective Friedel–Crafts Alkylation Reaction

    Marco Bandini;Alfonso Melloni;Achille Umani-Ronchi

  • A Journey Across Recent Advances in Catalytic and Stereoselective Alkylation of Indoles

    Marco Bandini;Alfonso Melloni;Simona Tommasi;Achille Umani-Ronchi

  • Catalytic asymmetric synthesis of homoallylic alcohols

    Anna Luisa Costa;Maria Giulia Piazza;Emilio Tagliavini;Claudio Trombini

  • Sequential One-Pot InBr3-Catalyzed 1,4- then 1,2-Nucleophilic Addition to Enones

    Marco Bandini;Pier Giorgio Cozzi;Massimo Giacomini;Paolo Melchiorre

  • Neue katalytische Methoden in der stereoselektiven Friedel‐Crafts‐Alkylierung

    Marco Bandini;Alfonso Melloni;Achille Umani‐Ronchi

  • Catalytic Asymmetric Friedel-Crafts Alkylations

    Marco Bandini;Achille Umani-Ronchi

  • Organometallic ring-opening reactions of N-acyl and N-alkoxycarbonyl lactams. Synthesis of cyclic imines

    Arianna Giovannini;Diego Savoia;Achille Umani-Ronchi

  • New versatile Pd-catalyzed alkylation of indoles via nucleophilic allylic substitution: controlling the regioselectivity.

    Marco Bandini;and Alfonso Melloni;Achille Umani-Ronchi

  • Highly Enantioselective Synthesis of Tetrahydro-β-Carbolines and Tetrahydro-γ-Carbolines Via Pd-Catalyzed Intramolecular Allylic Alkylation

    Marco Bandini;Alfonso Melloni;Fabio Piccinelli;Riccardo Sinisi

  • The First Catalytic Enantioselective Nozaki-Hiyama Reaction.

    Marco Bandini;Pier Giorgio Cozzi;Paolo Melchiorre;Achille Umani-Ronchi

  • Innovative Catalytic Protocols for the Ring‐Closing Friedel–Crafts‐Type Alkylation and Alkenylation of Arenes

    Marco Bandini;Enrico Emer;Simona Tommasi;Achille Umani‐Ronchi

  • Enantioselective Synthesis of Homoallylic Amines by Addition of Allylmetal Reagents to Imines Derived from (S)-Valine Esters

    Tiziana Basile;Allaye Bocoum;Diego Savoia;Achille Umani-Ronchi

  • Kinetic resolution of epoxides by a C-C bond-forming reaction: highly enantioselective addition of indoles to cis, trans, and meso aromatic epoxides catalyzed by [Cr(salen)] complexes.

    Marco Bandini;Pier Giorgio Cozzi;Paolo Melchiorre;Achille Umani-Ronchi

  • Highly enantioselective nitroaldol reaction catalyzed by new chiral copper complexes

    Marco Bandini;Fabio Piccinelli;Simona Tommasi;Achille Umani-Ronchi

  • [Cr(Salen)] as a ‘bridge’ between asymmetric catalysis, Lewis acids and redox processes

    Marco Bandini;Pier Giorgio Cozzi;Achille Umani-Ronchi

  • Catalytic asymmetric synthesis promoted by a chiral zirconate: Highly enantioselective allylation of aldehydes

    Paolo Bedeschi;Sonia Casolan;Anna L. Costa;Emilio Tagliavini

  • Recoverable PEG-supported copper catalyst for highly stereocontrolled nitroaldol condensation.

    Marco Bandini;Maurizio Benaglia;Riccardo Sinisi;and Simona Tommasi

  • Catalytic enantioselective conjugate addition of indoles to simple α,β-unsaturated ketones

    Marco Bandini;Matteo Fagioli;Paolo Melchiorre;Alfonso Melloni

  • Can simple enones be useful partners for the catalytic stereoselective alkylation of indoles

    Marco Bandini;Matteo Fagioli;Marco Garavelli;Alfonso Melloni

  • Salen as a Chiral Activator:anti versussyn Switchable Diastereoselection in the Enantioselective Addition of Crotyl Bromide to Aromatic Aldehydes

    Marco Bandini;Pier Giorgio Cozzi;Achille Umani-Ronchi

  • InBr3-catalyzed Friedel-Crafts addition of indoles to chiral aromatic epoxides: a facile route to enantiopure indolyl derivatives.

    Marco Bandini;Pier Giorgio Cozzi;Paolo Melchiorre;Achille Umani-Ronchi

Frequent Co-Authors

Pier Giorgio Cozzi
Pier Giorgio Cozzi University of Bologna
Marco Bandini
Marco Bandini University of Bologna
Paolo Melchiorre
Paolo Melchiorre Royal Society of Chemistry
Dario Braga
Dario Braga University of Bologna
Maurizio Benaglia
Maurizio Benaglia University of Milan
Michael O. Wolf
Michael O. Wolf University of British Columbia
Aldo Roda
Aldo Roda University of Bologna
Gian Piero Spada
Gian Piero Spada University of Bologna
Giovanna Barbarella
Giovanna Barbarella National Research Council (CNR)
Massimo Gazzano
Massimo Gazzano National Research Council (CNR)

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