S. Rizzo

发表

Natural-based chiral task-specific deep eutectic solvents: A novel, effective tool for enantiodiscrimination in electroanalysis

P. Mussini, L. Micheli, F. Arduini, 2021 .

An “inherently chiral” 1,1′-bibenzimidazolium additive for enantioselective voltammetry in ionic liquid media

F. Sannicolò, P. Mussini, A. Gennaro, 2018 .

Chirality in the absence of rigid stereogenic elements: the absolute configuration of residual enantiomers of C3-symmetric propellers.

F. Sannicolò, P. Mussini, T. Pilati, 2009, Chemistry.

Chirality in the absence of rigid stereogenic elements: the design of configurationally stable C3-symmetric propellers.

F. Sannicolò, T. Pilati, T. Benincori, 2009, Chemistry.

Advanced chiral molecular media for enantioselective electrochemistry and electroanalysis

P. Mussini, S. Arnaboldi, Sara Grecchi, 2021, Current Opinion in Electrochemistry.

Towards molecular design rationalization in branched multi-thiophene semiconductors: the 2-thienyl-persubstituted alpha-oligothiophenes.

F. Sannicolò, P. Mussini, M. Muccini, 2010, Chemistry.

Influence of the nature of alkyl substituents on the high-performance liquid chromatography enantioseparation and retention of new atropisomeric 1,1'-bibenzimidazole derivatives on amylose tris(3,5-dimethylphenylcarbamate) chiral stationary phase.

R. Cirilli, Sergio Menta, C. Faggi, 2014, Journal of chromatography. A.

Electrocatalytic reduction of bromothiophenes on gold and silver electrodes: An example of synergy in electrocatalysis

P. Mussini, A. Gennaro, T. Benincori, 2018 .

A family of chiral ionic liquids from the natural pool: Relationships between structure and functional properties and electrochemical enantiodiscrimination tests

P. Mussini, C. Chiappe, S. Arnaboldi, 2019, Electrochimica Acta.

Helicity: A Non-Conventional Stereogenic Element for Designing Inherently Chiral Ionic Liquids for Electrochemical Enantiodifferentiation

P. Mussini, L. Micheli, F. Fontana, 2021, Molecules.

Free design of chiral diphosphine chelating ligands for stereoselective homogeneous catalysis by assmbling five‐membered atomatic heterocycles

T. Benincori, S. Rizzo, F. Sannicò, 2002 .

2,12-Diaza[6]helicene: An Efficient Non-Conventional Stereogenic Scaffold for Enantioselective Electrochemical Interphases

P. Mussini, L. Micheli, M. Tommasini, 2021, Chemosensors.

Ph‐tetraMe‐Bithienine, the First Member of the Class of Chiral Heterophosphepines: Synthesis, Electronic and Steric Properties, Metal Complexes and Catalytic Activity

F. Sannicolò, P. Mussini, T. Pilati, 2013 .

Enantioselective hydrogenation of diaryl-substituted α,β-unsaturated nitriles

A. Buschauer, T. Benincori, O. Reiser, 2006 .

An Electrochemically Prepared Small-Bandgap Poly(biheteroarylidenemethine): Poly{bi[(3,4-ethylenedioxy)thienylene]methine}

G. Zotti, S. Zecchin, T. Benincori, 2003 .

Steric and electronic tuning of chiral bis(oxazoline) ligands with 3,3'-bithiophene backbone.

P. Mussini, T. Pilati, T. Benincori, 2005, The Journal of organic chemistry.

2,5-Dimethyl-3,4-bis[(2R,5R)-2,5-dimethylphospholano]thiophene: first member of the hetero-DuPHOS family.

M. Burk, T. Pilati, T. Benincori, 2005, The Journal of organic chemistry.

A new modular class of easily accessible, inexpensive, and efficient chiral diphosphine ligands for homogeneous stereoselective catalysis.

F. Sannicolò, T. Benincori, S. Gladiali, 2001, The Journal of organic chemistry.

Determination of the Enantiomerization Barrier of the Residual Enantiomers of C3 -Symmetric Tris[3-(1-Methyl-2-Alkyl)Indolyl]Phosphane Oxides: Case Study of a Multitasking HPLC Investigation Based on an Immobilized Polysaccharide Stationary Phase.

F. Sannicolò, T. Benincori, R. Cirilli, 2015, Chirality.

Steric and electronic effects on the configurational stability of residual chiral phosphorus-centered three-bladed propellers: tris-aryl phosphanes.

F. Sannicolò, P. Mussini, T. Pilati, 2013, Chemistry.

Potential-driven chirality manifestations and impressive enantioselectivity by inherently chiral electroactive organic films.

W. Kutner, F. Sannicolò, P. Mussini, 2014, Angewandte Chemie.

Process-scale preparation of enantiomerically pure γ-lactones by asymmetric hydrogenation of γ-ketoesters and comparative tests of the sensory properties of some antipodes

T. Pilati, T. Benincori, E. Pagliarini, 2004 .

A Raman and SERS study on the interactions of aza[5]helicene and aza[6]helicene with a nanostructured gold surface

M. Tommasini, F. Fontana, A. Lucotti, 2020, Vibrational Spectroscopy.

BITHIENOLs: new promising C2-symmetric bis-heteroaromatic diols for organic transformations

T. Benincori, R. Cirilli, S. Rossi, 2016 .

Calix[4]arene-functionalized poly-cyclopenta[2,1-b;3,4-b']bithiophenes with good recognition ability and selectivity for small organic molecules for application in QCM-based sensors

Sandro Zecchin, Tiziana Benincori, G. Zotti, 2004 .

Inherently Chiral Macrocyclic Oligothiophenes: Easily Accessible Electrosensitive Cavities with Outstanding Enantioselection Performances

F. Sannicolò, P. Mussini, T. Benincori, 2014, Chemistry.

An effective multipurpose building block for 3D electropolymerisation: 2,2 -Bis(2,2 -bithiophene-5-yl)-3,3 -bithianaphthene

W. Kutner, F. Sannicolò, P. Mussini, 2010 .

"Inherently Chiral" Ionic-Liquid Media: Effective Chiral Electroanalysis on Achiral Electrodes.

F. Sannicolò, P. Mussini, A. Gennaro, 2017, Angewandte Chemie.

Electrochemistry and Chirality in Bibenzimidazole Systems

F. Sannicolò, P. Mussini, A. Gennaro, 2015 .

Configurationally Stable Molecular Propellers: First Resolution of Residual Enantiomers†

Tullio Pilati, Alessandro Ponti, Giuseppe Celentano, 2006 .

Diels–Alder reactions of enantiopure [(1S)-isoborneol-10-sulfinyl]- and [(1S-exo)-2-bornylsulfinyl]vinylcyclohexenes with maleimides

F. Nicolò, P. Bonaccorsi, A. Barattucci, 1999 .

Diels–Alder reactions of (RS)-3-[(1S)-isoborneol-10-sulfinyl]-1-methoxybuta-1,3-dienes with electron-deficient carbodienophiles. The effects of Lewis acid catalysis

P. Bonaccorsi, A. Barattucci, S. Rizzo, 1998 .

Diels—Alder Reactions of Enantiopure [(1S)-Isoborneol-10-sulfinyl]- and [(1S-exo)-2-Bornylsulfinyl]vinylcyclohexenes with Maleimides.

F. Nicolò, P. Bonaccorsi, A. Barattucci, 2010 .

Diels—Alder Reactions of (RS)-3-[(1S)-Isoborneol-10-sulfinyl]-1-methoxybuta-1,3-dienes with Electron-Deficient Carbodienophiles. The Effects of Lewis Acid Catalysis.

P. Bonaccorsi, A. Barattucci, S. Rizzo, 1998 .

Electronic Tuning in C1-Symmetric Chelating Diphosphane Ligands Supported on Stereogenic Aryl-Heteroaryl Templates

G. Zotti, T. Benincori, S. Gladiali, 2001 .

Potential-driven chirality manifestations and impressive enantioselectivity by inherently chiral electroactive organic films.

W. Kutner, F. Sannicolò, P. Mussini, 2014, Angewandte Chemie.

HPLC Enantioseparation of Rigid Chiral Probes with Central, Axial, Helical, and Planar Stereogenicity on an Amylose (3,5-Dimethylphenylcarbamate) Chiral Stationary Phase

D. Pasini, T. Benincori, F. Fontana, 2022, Molecules.