H
Henriette Molinari
Researcher at University of Verona
Publications - 128
Citations - 4020
Henriette Molinari is an academic researcher from University of Verona. The author has contributed to research in topics: Nuclear magnetic resonance spectroscopy & Ligand (biochemistry). The author has an hindex of 31, co-authored 125 publications receiving 3734 citations. Previous affiliations of Henriette Molinari include University of Milano-Bicocca.
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The Poisson-Boltzmann equation for biomolecular electrostatics: a tool for structural biology.
TL;DR: An ever‐increasing body of successful applications proves that the Poisson–Boltzmann equation is a useful tool for structural biology and complementary to other established experimental and theoretical methodologies.
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Synthetic enzymes. Part 2. Catalytic asymmetric epoxidation by means of polyamino-acids in a triphase system
Sebastián Juliá,Joan Guixer,Jaume Masana,José Rocas,Stefano Colonna,Rita Annuziata,Henriette Molinari +6 more
TL;DR: In this article, the asymmetric epoxidation of several chalcones and other electron-poor olefins, in the presence of catalytic amounts of poly-(S)-amino-acids in a triphase system with optical yields of up to 96% is described.
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Protocol for MM/PBSA molecular dynamics simulations of proteins.
TL;DR: A fast and reliable methodology to implement continuum forces in standard molecular mechanics and dynamics algorithms is proposed and results for a totally unrestrained 1 ns molecular dynamics simulation of a small protein are quantitatively similar to results obtained by explicit solvent molecular dynamics simulations.
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Synthetic enzymes—4
TL;DR: In this article, the influence of the molecular structure of catalysts and of their secondary conformation on the enantioselectivity of chalcone and other electron-poor olefins in a triphase system was examined.
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Asymmetric epoxidation of electron-poor olefins-V: Influence on stereoselectivity of the structure of poly-α-aminoacids used as catalysts
TL;DR: In this article, new poly-α-aminoacids modified at the C or N -terminal groups were synthetised and employed in the asymmetric epoxidation of chalcone.