Michael Andresini

Dr. Michael Andresini

orcid

Research Focus & Metrics

Academic Career Length

9Years (2018-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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3 May 2022 in Chemical Communications
Verified
Journal Article
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PMPantaleo Musci
Pantaleo Musci
Marco ColellaMarco Colella
Marco Colella
MAMichael Andresini
Michael Andresini
AAAndrea Aramini
Andrea Aramini
Leonardo DegennaroLeonardo Degennaro
Leonardo Degennaro
Renzo LuisiRenzo Luisi
Renzo Luisi
The use of flow technology as an enabling tool for accessing 1-azabicyclo[1.1.0]butanes bearing strained 3-, 4-, and 5-membered O-heterocycles with C3 (N-het) –C2 (O-het) connectivity is reported.

28 November 2023 in Journal of Flow Chemistry
Verified
Journal Article
Closed access
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MSMauro Spennacchio
Mauro Spennacchio
Philipp NathoPhilipp Natho
Philipp Natho
MAMichael Andresini
Michael Andresini
Marco ColellaMarco Colella
Marco Colella

13 August 2021 in Organic Letters
Verified
Journal Article
Closed access
MAMichael Andresini
Michael Andresini
MSMauro Spennacchio
Mauro Spennacchio
Marco ColellaMarco Colella
Marco Colella
GLGianluca Losito
Gianluca Losito
AAAndrea Aramini
Andrea Aramini
Renzo LuisiRenzo Luisi
Renzo Luisi

13 September 2023 in Organic & Biomolecular Chemistry
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Journal Article
Closed access
PDF file
MAMichael Andresini
Michael Andresini
Marco ColellaMarco Colella
Marco Colella
LDLeonardo Degennaro
Leonardo Degennaro
Renzo LuisiRenzo Luisi
Renzo Luisi
Significant advancements have recently been made in the chemistry of sulfinamidines and sulfinimidate esters. This review aims to provide an overview of the synthetic methods for the preparation and transformation of these overlooked compounds.

28 March 2024 in Organic Letters
Verified
Journal Article
Open access
Philipp NathoPhilipp Natho
Philipp Natho
Marco ColellaMarco Colella
Marco Colella
MAMichael Andresini
Michael Andresini
Leonardo DegennaroLeonardo Degennaro
Leonardo Degennaro
Renzo LuisiRenzo Luisi
Renzo Luisi
The oxetane ring has evolved as a useful bioisostere for dimethyl and carbonyl groups for the improvement of physiochemical properties of drug candidates. Herein, we report the generation and utilization of highly unstable 3-oxetanyllithium as a hitherto unexplored nucleophile leveraging flash technology. A range of different electrophiles are suitable reaction partners in this protocol, and we demonstrate the utility of this protocol in late-stage pharmaceutical analogue synthesis.

12 May 2022 in Organic & Biomolecular Chemistry
Verified
Journal Article
Closed access
PDF file
Marco ColellaMarco Colella
Marco Colella
PMPantaleo Musci
Pantaleo Musci
MAMichael Andresini
Michael Andresini
MSMauro Spennacchio
Mauro Spennacchio
Leonardo DegennaroLeonardo Degennaro
Leonardo Degennaro
Renzo LuisiRenzo Luisi
Renzo Luisi
This minireview covers the recent relevant literature updates on the use of CH 2 FI as readily available platform for monofluoromethylation strategies.