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Cecilia Pinna

Researcher at University of Milan

Publications -  8
Citations -  168

Cecilia Pinna is an academic researcher from University of Milan. The author has contributed to research in topics: Chemistry & Medicine. The author has an hindex of 3, co-authored 4 publications receiving 52 citations.

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An overview of coumarin as a versatile and readily accessible scaffold with broad-ranging biological activities

TL;DR: This review is intended to be a critical overview on coumarins, comprehensive of natural sources, metabolites, biological evaluations and synthetic approaches.
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Efficient chemo-enzymatic flow synthesis of high value amides and esters

TL;DR: A flow-based chemo-enzymatic synthesis of selected APIs (i.e., butacaine, procaine and procainamide) has been developed, demonstrating high stability and reusability and making the process fast, safe and easily handled.
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Biocatalyzed Flow Oxidation of Tyrosol to Hydroxytyrosol and Efficient Production of Their Acetate Esters.

TL;DR: In this article, a sustainable, biocatalyzed flow protocol was developed for the chemo-and regio-selective oxidation of Ty into HTy catalyzed by free tyrosinase from Agaricus bisporus in a gas/liquid biphasic system.
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Biocatalytic Approaches for an Efficient and Sustainable Preparation of Polyphenols and Their Derivatives.

TL;DR: In this paper, an overview of the potential of biocatalysis as a powerful tool for the modification of polyphenols to enhance their bioaccessibility, bioavailability, biological activity or modification of their physicochemical properties is presented.
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Investigation of the Effects of Monomeric and Dimeric Stilbenoids on Bacteria-Induced Cytokines and LPS-Induced ROS Formation in Bone Marrow-Derived Dendritic Cells

TL;DR: In this paper , the authors compared five monomeric (resveratrol, piceatannol, pterostilbene, pinostil bene, and trimethoxy-reserveratrol) and two dimeric stilbenoids for their capability to modulate the production of bacteria-induced IL-12, IL-10, and TNF-α in murine bone marrow-derived dendritic cells.