MS
Mattia Silvi
University of Nottingham, University of Bristol, Institut Català d'Investigació Química, Sapienza University of Rome
Research areas: Chemistry · Organic Chemistry · Radical Photochemical Reactions · Asymmetric Synthesis and Catalysis · Organic Chemistry Synthesis Methods
0000-0002-0728-7193
Employment
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University of Nottingham Nottingham Research Fellow2019 - Present
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University of Bristol Research Associate2019 - 2019
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University of Bristol Marie Skłodowska-Curie IF Fellow2017 - 2019
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University of Bristol Research Associate2016 - 2017
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Institut Català d'Investigació Química Post-Doctoral Researcher2015 - 2015
Education
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Institut Català d'Investigació Química Doctoral Degree2011 - 2015
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Università degli Studi di Roma La Sapienza MSc in Organic Chemistry2008 - 2011
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Università degli Studi di Roma La Sapienza BSc in Analytical Chemistry2004 - 2008
Projects & Funding
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Light-Driven Multicomponent C-C Couplings: New Avenues to Bioactive Molecules Engineering and Physical Sciences Research Council2021 - 2023
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Nottingham Research Fellowship University Of Nottingham2019 - 2022
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PHOTO-BORAD European Commission2017 - Present
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ICIQ - UM Global Engagement Program Fellowship Institut Català d'Investigació Química - University of Michigan2014 - 2014
Publications (18)
- Polarity Transduction Enables the Formal Electronically Mismatched Radical Addition to Alkenes Save
- The Conceptual Development of a Conjunctive Olefination Save
- Visible light-driven conjunctive olefination Save
- Visible Light-Driven Strain-Increase Ring Contraction Allows the Synthesis of Cyclobutyl Boronic Esters Save
- Radical Addition to Strained σ-Bonds Enables the Stereocontrolled Synthesis of Cyclobutyl Boronic Esters Save
- Enantiospecific Three-Component Alkylation of Furan and Indole Save
- Direct Stereoselective Installation of Alkyl Fragments at the β-Carbon of Enals via Excited Iminium Ion Catalysis Save
- Enhancing the potential of enantioselective organocatalysis with light Save
- Reoptimization of the Organocatalyzed Double Aldol Domino Process to a Key Enal Intermediate and Its Application to the Total Synthesis of Δ12-Prostaglandin J<inf>3</inf> Save
- Merging Photoredox with 1,2-Metallate Rearrangements: The Photochemical Alkylation of Vinyl Boronate Complexes Save
- Enantioselective Formal α-Methylation and α-Benzylation of Aldehydes by Means of Photo-organocatalysis Save
- Visible-light excitation of iminium ions enables the enantioselective catalytic β-alkylation of enals Save
- Enamine-Mediated Catalysis (n?→?π*) Save
- Synthesis of Cyclic Guanidines via Silver-Catalyzed Intramolecular Alkene Hydroamination Reactions of N-Allylguanidines Save
- Enantioselective Organocatalytic Alkylation of Aldehydes and Enals Driven by the Direct Photoexcitation of Enamines Save
- Controlling the Molecular Topology of Vinylogous Iminium Ions by Logical Substrate Design: Highly Regio- and Stereoselective Aminocatalytic 1,6-Addition to Linear 2,4-Dienals Save
- Enantioselective aza-Michael addition of imides by using an integrated strategy involving the synthesis of a family of multifunctional catalysts, usage of multiple catalysis, and rational design of experiment Save
- Secondary Amine-Catalyzed Asymmetricγ-Alkylation ofα-Branched EnalsviaDienamine Activation Save