M
Matteo Minozzi
Researcher at University of Bologna
Publications - 43
Citations - 1160
Matteo Minozzi is an academic researcher from University of Bologna. The author has contributed to research in topics: Radical & Aryl. The author has an hindex of 21, co-authored 43 publications receiving 1101 citations.
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From azides to nitrogen-centered radicals: applications of azide radical chemistry to organic synthesis.
TL;DR: Over the last thirty years organic azides have drawn a great deal of attention as radical traps for carbon- and heteroatom-centered radicals, both in intra- and in intermolecular processes.
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Approach to Spirocyclohexadienimines and Corresponding Dienones through Radical ipso Cyclization onto Aromatic Azides
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An Insight into the Radical Thiol/Yne Coupling: The Emergence of Arylalkyne-Tagged Sugars for the Direct Photoinduced Glycosylation of Cysteine-Containing Peptides
Matteo Minozzi,Alessandro Monesi,Daniele Nanni,Piero Spagnolo,Nicola Marchetti,Alessandro Massi +5 more
TL;DR: The glycosylation of the tripeptide glutathione in its native form was successfully applied, under physiological conditions, to a cysteine-containing nonapeptide with marked advantages over the analogous Thiol-Ene Coupling (TEC) derivatization.
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Generation and intramolecular reactivity of acyl radicals from alkynylthiol esters under reducing tin-free conditions.
Luisa Benati,Gianluca Calestani,Rino Leardini,Matteo Minozzi,Daniele Nanni,Piero Spagnolo,Samantha Strazzari +6 more
TL;DR: The radical chain reaction of benzenethiol with alkynylthiol esters provides a new, valuable protocol for the tin-free generation of acyl radicals that arise from intramolecular substitution at sulfur by the initial sulfanylvinyl radicals.
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Reaction of azides with dichloroindium hydride: very mild production of amines and pyrrolidin-2-imines through possible indium-aminyl radicals.
Luisa Benati,Giorgio Bencivenni,Rino Leardini,Daniele Nanni,Matteo Minozzi,Piero Spagnolo,Rosanna Scialpi,Giuseppe Zanardi +7 more
TL;DR: A rationalization of the overall experimental data cannot exclude the occurrence of competitive radical and nonradical pathways, but certain results are soundly consistent with the intermediacy of indium-bound nitrogen-centered radicals.