A
Andrea Milelli
Researcher at University of Bologna
Publications - 61
Citations - 1928
Andrea Milelli is an academic researcher from University of Bologna. The author has contributed to research in topics: GSK-3 & Tacrine. The author has an hindex of 20, co-authored 56 publications receiving 1650 citations. Previous affiliations of Andrea Milelli include National Research Foundation of South Africa.
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Journal ArticleDOI
Tacrine derivatives and Alzheimer's disease.
Vincenzo Tumiatti,Anna Minarini,Maria Laura Bolognesi,Andrea Milelli,Michela Rosini,Carlo Melchiorre +5 more
TL;DR: This review will focus on and summarize the last two years of research into the development of tacrine derivatives able to hit AD targets beyond simple AChE inhibition.
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Oxidative Stress in Alzheimer’s Disease: Are We Connecting the Dots?
TL;DR: Significant progress in the field of antioxidant research is highlighted, including the fine-tuned equilibrium between antioxidant defenses and free radical production, the lack of specific antioxidant target(s), and the inherent difficulty in delivering antioxidants where they are needed.
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Organocatalytic Asymmetric Synthesis of α,α-Disubstituted α-Amino Acids and Derivatives
Silvia Cabrera,Efraim Reyes,José Alemán,Andrea Milelli,Sara Kobbelgaard,Karl Anker Jørgensen +5 more
TL;DR: It is shown that racemic oxazolones are excellent reagents for the synthesis of chiral quaternary amino acids and its derivatives by the diastereo- and enantioselective nucleophilic addition to alpha,beta-unsaturated aldehydes catalyzed by diarylprolinol silyl ethers.
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How to make five contiguous stereocenters in one reaction: asymmetric organocatalytic synthesis of pentasubstituted cyclohexanes.
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Asymmetric 1,4‐Addition of Oxazolones to Nitroalkenes by Bifunctional Cinchona Alkaloid Thiourea Organocatalysts: Synthesis of α,α‐Disubstituted α‐Amino Acids
TL;DR: An easy and simple synthetic approach to optically active alpha,alpha-quaternary alpha-amino acids using asymmetric organocatalysis is presented and additional transformations are presented, such as the synthesis of amino esters, amino acids, and transformation into 3,4-disubstituted pyrrolidin-2-ones.