Voichita Mihali
Zürcher Fachhochschule
23 Papers
119 Citations
Voichita Mihali is an academic researcher from Zürcher Fachhochschule. The author has contributed to research in topics: Chirality (chemistry) & Stereocenter. The author has an hindex of 8, co-authored 19 publications. Previous affiliations of Voichita Mihali include University of Milan.
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Papers
“Inherently Chiral” Ionic-Liquid Media: Effective Chiral Electroanalysis on Achiral Electrodes
Simona Rizzo,Serena Arnaboldi,Voichita Mihali,Roberto Cirilli,Alessandra Forni,Armando Gennaro,Abdirisak Ahmed Isse,Marco Pierini,Patrizia R. Mussini,Francesco Sannicolò +9 more
TL;DR: Inherently chiral ionic liquids (ICILs) have now been prepared starting from atropisomeric 3,3'-bicollidine, synthesized from inexpensive reagents, resolved into antipodes without need of chiral HPLC and converted into long-chain dialkyl salts with melting points below room temperature.
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Highly stereoselective intramolecular α-arylation of self-stabilized non-racemic enolates: synthesis of α-quaternary α-amino acid derivatives
TL;DR: The 'one-pot' stereoselective conversion of N-(4-nitrobenzene)sulfonyl-alpha-amino acid tert-butyl esters into the corresponding N-alkyl-alpha-( 4-nitrophenyl)-alpha- amino esters has been realized through N-alksylation of the starting amido esters.
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pH-Responsive Pickering Foams Generated by Surfactant-Free Soft Hydrogel Particles.
TL;DR: This work synthesized surfactant-free biocompatible poly[2(diethylamino)ethyl methacrylate] (PDEAEMA) hydrogel particles (HGPs) by emulsion polymerization by defining the morphology, structure, and surface charge of the HGPs by TEM, DLS, and the zeta potential.
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Enantioselective Rearrangement of Proline Sulfonamides: An Easy Entry to Enantiomerically Pure α-Aryl Quaternary Prolines
Francesca Foschi,Dario Landini,Vittoria Lupi,Voichita Mihali,Michele Penso,Tullio Pilati,Aaron Tagliabue +6 more
TL;DR: A highly enantioselective rearrangement of proline-derived sulfonamides proceeds in the presence of base to give α-arylprolines with a quaternary stereocenter in up to 96% optical purity.
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Memory of chirality approach to the enantiodivergent synthesis of chiral benzo[d]sultams.
TL;DR: The interest of this protocol resides in the possibility of using the chirality of a starting sulfonamide single enantiomer to synthesize the target sultams in both absolute configurations, by using different base systems, under homogeneous conditions.
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