F. Viani

发表

L-Amino acid amides via dynamic kinetic resolution

S. Servi, Davide Tessaro, P. D’Arrigo, 2011 .

Base catalyzed racemization of amino acid derivatives

S. Servi, Davide Tessaro, P. D’Arrigo, 2011 .

Synthesis and use of (E)-1-ethoxy-3-fluoroalkyl-3-hydroxy-4-(4-methylphenylsulfinyl)but-1-enes

V. Kukhar, S. V. Meille, I. Gerus, 1995 .

New fluorinated chiral synthons

S. V. Meille, V. Soloshonok, M. Frigerio, 1994 .

Synthesis of Nonracemic α‐Trifluoromethyl α‐Amino Acids from Sulfinimines of Trifluoropyruvate

S. V. Meille, A. Volonterio, M. Zanda, 2001 .

Experimental Evidence for Intramolecular Attractive Nonbonded C–F…H–C Interactions in 2′,3′-Dideoxy-4′-(fluoromethyl)nucleosides – Through-Space JCF and JHF NMR Coupling Constants, Correlation with Empirical Parameters of Solvent Polarity and Single-Crystal X-ray Structures

B. Vergani, A. Mele, S. V. Meille, 1999 .

Synthesis and anti-bacterial activity of a library of 1,2-benzisothiazol-3(2H)-one (BIT) derivatives amenable of crosslinking to polysaccharides

W. Panzeri, L. Merlini, A. Martorana, 2017 .

Mild α-fluorination of enantiomerically pure β-ketosulfoxides by F-TEDA-BF4

M. Zanda, A. Arnone, C. Zappalà, 1997 .

Synthesis of 3′-Arylsulfonyl-4′-[(diethoxyphosphoryl)difluoromethyl]thymidine

A. Arnone, C. Zappalà, M. Frigerio, 1998 .

Stereoselective Synthesis of Fluorinated Isoxazolidines and 2,3-Dihydroisoxazoles: A Cycloadditive Route to Enantiomerically Pure Amino Fluoro Alcohols

W. Panzeri, A. Arnone, F. Viani, 1999 .

Chiral sulfoxide controlled asymmetric additions to CN double bond. An efficient approach to stereochemically defined α-fluoroalkyl amino compounds

M. Zanda, V. Soloshonok, A. Sorochinsky, 1998 .

Synthesis of 2‐Fluoro Analogues of Frontalin

W. Panzeri, M. Frigerio, A. Sekine, 2000 .

Highly diastereoselective methylene transfer from diazomethane to the carbonyl of β-keto sulfoxides. A general approach to synthetically versatile fluorine-containing chiral building blocks

A. Arnone, V. Soloshonok, M. Frigerio, 1998 .

Synthesis and reactivity of enantiomerically pure 2-fluoromethyl-2-(1′-p-tolylsulfinyl)alkyl oxiranes

A. Arnone, V. Soloshonok, M. Frigerio, 1998 .

SYNTHESIS OF SELECTIVELY FLUORINATED MOLECULES FROM DIMETHYLSULFOXIDE, FLUOROACETIC ACID ESTERS AND DIAZOMETHANE

W. Panzeri, F. Viani, P. Bravo, 1998 .

EPC synthesis of gem-difluorocyclopentane derivatives

M. Frigerio, F. Viani, G. Cavicchio, 1992 .

Through‐Space 7JHF and 6JCF Spin–Spin Couplings in 2′,3′‐Dideoxy‐4′‐fluoroalkylnucleosides. The Role of Sugar Ring Conformation and Solvent Effect

A. Mele, G. Salani, F. Viani, 1997 .

Stereoselective synthesis of trifluoro- and monofluoro-analogues of frontalin and evaluation of their biological activity.

P. Roversi, P. Ambrosi, M. Zanda, 2001, The Journal of organic chemistry.

The Influence of Fluorinated Molecules (Semiochemicals and Enzyme Substrate Analogues) on the Insect Communication System

F. Viani, C. Pesenti, 2004, Chembiochem : a European journal of chemical biology.

Homochiral fluoroorganic compounds. Part 17. 2-(p-Tolylsulphinylmethyl)-3-fluorotetrahydro-pyrans and -furans through intramolecular oxymercuriation

G. Resnati, A. Arnone, F. Viani, 1991 .

Asymmetric synthesis of α-arylglycinols via additions of lithium methyl p-tolyl sulfoxide to N-(PMP)arylaldimines followed by “non oxidative” Pummerer reaction

S. V. Meille, M. Zanda, V. Soloshonok, 1999 .

STEREOSELECTIVE ADDITIONS OF ALPHA -LITHIATED ALKYL-P-TOLYLSULFOXIDES TO N-PMP(FLUOROALKYL)ALDIMINES. AN EFFICIENT APPROACH TO ENANTIOMERICALLY PURE F LUORO AMINO COMPOUNDS

S. V. Meille, M. Zanda, V. Soloshonok, 1997 .

Stereocontrolled synthesis of hydroxyethylamine isosteres via chiral sulfoxide chemistry

S. V. Meille, M. Zanda, W. Panzeri, 2004 .

Synthesis of (+)- and (-)-statine via chiral sulfoxide chemistry.

S. V. Meille, M. Zanda, W. Panzeri, 2001, The Journal of organic chemistry.

Synthesis of Enantiomerically Pure 2′,3′,5′‐Trideoxy‐4′‐[(diethoxyphosphoryl)difluoromethyl]thymidine Analogues

B. Vergani, A. Mele, A. Arnone, 1999 .

Synthesis of optically pure (R)- and (S)-α-trifluoromethyl-alanine

S. V. Meille, M. Zanda, V. Soloshonok, 1994 .

Stereoselective Synthesis of the Pheromone (R)-(–)-Sulcatol, and Its Enantiopure (R)- and (S)-1-Mono-, -1,1-Di-, and -1,1,1-Trifluoro Analogues[1]

M. Zanda, W. Panzeri, A. Arnone, 1999 .

Synthesis and reactions of enantiomerically pure chloromethyl oxiranes

M. Zanda, M. Frigerio, F. Viani, 1996 .

Synthesis of fluorinated chirons: Stereoselective oxirane formation by reaction of diazomethane on 1-fluoro-3-arylsulfinyl-2-propanone and ring opening by selected nucleophiles

A. Arnone, C. Zappalà, M. Frigerio, 1995 .

A new versatile fluorinated C4 chiron

A. Arnone, C. Zappalà, M. Frigerio, 1992 .

Synthesis of optically pure fluoro- and gem-chlorofluoro-cyclohexane derivatives by intramolecular trapping of dihaloalkyl radicals.

A. Arnone, M. Frigerio, F. Viani, 1992 .

Synthesis of optically pure α-methylene-γ-lactones from (+)-R-(4-methylphenyl)-alkylsulphoxides

G. Resnati, F. Viani, P. Bravo, 1985 .

Total synthesis of a pepstatin analog incorporating two trifluoromethyl hydroxymethylene isosteres (Tfm-GABOB) and evaluation of Tfm-GABOB containing peptides as inhibitors of HIV-1 protease and MMP-9

S. V. Meille, M. Zanda, W. Panzeri, 2001 .

Stereocontrolled approaches to (+)- and (−)-γ-trifluoromethyl-GABOB, a new hydroxymethylene (statine) dipeptide isostere

B. Vergani, A. Volonterio, M. Zanda, 1998 .

Optically pure and fluoro substituted carboacyclic nucleoside analogues

V. Soloshonok, M. Frigerio, F. Viani, 1993 .

Homochiral 2,5-disubstituted 3-fluorotetrahydrofurans carrying differently functionalized ring appendages

G. Resnati, A. Arnone, F. Viani, 1989 .

Asymmetric synthesis of gem-chlorofluorocyclopentane derivatives by intramolecular trapping of dihaloalkyl radicals

A. Arnone, M. Frigerio, F. Viani, 1993 .

On the preparation of disymmetrized tris(hydroxymethyl) methanol equivalents

S. V. Meille, A. Arnone, M. Frigerio, 1995 .

Replacement of Isobutyl by Trifluoromethyl in Pepstatin A Selectively Affects Inhibition of Aspartic Proteinases

L. Prade, M. Zanda, C. Binkert, 2006, Chembiochem : a European journal of chemical biology.

Solution and solid-phase synthesis of trifluoromethyl peptides and mimetics

A. Volonterio, M. Zanda, F. Viani, 2001 .

Total synthesis of a Pepstatin analogue incorporating two trifluoromethyl hydroxymethylene isosteres

M. Zanda, W. Panzeri, A. Arnone, 2000 .

Synthesis of both enantiomers of optically pure saturated and α,β-unsaturated γ-substituted γ-lactones from chiral sulphoxides. X-Ray molecular structure of (3R,4S)-4-methyl-4-t-butyl-3-(p-tolylthio)butanolide and of (3R,4R)-4-(cyclohex-1-enyl)-4-methyl-3-(p-tolylthio)butanolide

G. Resnati, A. Albinati, F. Ganazzoli, 1986 .

Traceless solid-phase synthesis of 2,4,6-chlorodiamino and triaminopyrimidines

A. Wagner, A. Volonterio, C. Mioskowski, 2003 .

Chiroptical phenomena in reverse micelles: the case of (1R,2S)-dodecyl (2-hydroxy-1-methyl-2-phenylethyl)dimethylammonium bromide (DMEB).

F. Castiglione, A. Mele, G. Longhi, 2014, Chirality.

Unimolecular decomposition of M+. and [M+H]+ species of some fluorosubstituted acyclic nucleoside analogs.

P. Traldi, D. Favretto, F. Viani, 1991, Rapid communications in mass spectrometry : RCM.

Enzyme oxidation of plant galactomannans yielding biomaterials with novel properties and applications, including as delivery systems

T. Silvetti, M. Brasca, P. Campia, 2018, Applied Microbiology and Biotechnology.

Synergy between catalysts : enzymes and bases. DKR of non-natural amino acids derivatives

S. Servi, Davide Tessaro, P. D’Arrigo, 2012 .

SYNTHETICALLY USEFUL C-4 FLUORINATED BUILDING BLOCKS BEARING A QUATERNARY STEREOCENTRE

A. Arnone, M. Frigerio, G. Salani, 1994 .

Synthetically Useful C‐4 Fluorinated Building Blocks Bearing a Quaternary Stereocenter.

A. Arnone, M. Frigerio, G. Salani, 1995 .

Synthesis of Enantiomerically Pure gem-Difluorocyclohexane Derivatives by Intramolecular Trapping of .alpha.,.alpha.-Difluoroalkyl Radicals

A. Arnone, M. Frigerio, M. Crucianelli, 1994 .

Optically pure and fluoro substituted acyclovir analogues

G. Resnati, F. Viani, P. Bravo, 1993 .

Synthesis and pharmacological evaluation of enantiomerically pure 4-deoxy-4-fluoromuscarines.

G. Marucci, G. Resnati, A. Arnone, 1992, Journal of medicinal chemistry.

Intramolecular trapping of difluoroalkyl radicals by tethered olefin in the asymmetric synthesis of 2,4-disubstituted-3,3-difluorotetrahydrofurans

A. Arnone, F. Viani, P. Bravo, 1991 .

ON THE SYNTHESIS OF OPTICALLY PURE MONOFLUOROCYCLOHEXANOL DERIVATIVES BY THE FLUORINATED SULFOXIDE CHIRON ROUTE

A. Arnone, M. Frigerio, M. Crucianelli, 1994 .

Synthesis of 4'-Fluoroalkyl Nucleoside Analogues

A. Mele, G. Salani, P. L. Colla, 1995 .

Asymmetric synthesis of enantiomerically pure 4′-fluoroalkyl-2,3′-dideoxy nucleosides

A. Mele, F. Viani, P. Bravo, 1994 .

Asymmetric Synthesis of Enantiomerically Pure 4′-Fluoroalkyl-2′,3′- Dideoxy Nucleosides.

A. Mele, G. Salani, F. Viani, 1995 .

SYNTHESIS OF ENANTIOMERICALLY PURE 1',2'-SECO-AND 1',2'-SECO-2'-NOR-NUCLEOSIDES CARRYING FLUORINE AND SULPHUR SUBSTITUENTS

G. Resnati, F. Viani, P. Bravo, 1992 .

Influence of different ionization conditions on the mass spectrometric behaviour of some fluorinated acyclic nucleoside analogs

P. Traldi, Á. Somogyi, D. Favretto, 1995 .

Synthesis of Enantiomerically Pure 1′,2′‐seco‐ and 1′,2′‐seco‐2′‐nor‐ Nucleosides Carrying Fluorine and Sulfur Substituents.

G. Resnati, F. Viani, P. Bravo, 1993 .

Electron impact mass spectrometry of hemiterpenoid tricyclic quinoline alkaloids

P. Traldi, G. Resnati, A. Sturaro, 1987 .

Multifunctional Neomycin-Triazine-Based Cationic Lipids for Gene Delivery with Antibacterial Properties

N. Bono, Federica Ponti, G. Candiani, 2021, Bioconjugate chemistry.

Synthesis and Conformational Analysis of Hydantoin-Based Universal Peptidomimetics.

M. Mori, F. Meneghetti, A. Volonterio, 2022, The Journal of organic chemistry.

Stereoselective Additions of α‐Lithiated Alkyl‐p‐tolylsulfoxides to N‐PMP(Fluoroalkyl)aldimines. An Efficient Approach to Enantiomerically Pure Fluoro Amino Compounds.

S. V. Meille, M. Zanda, V. Soloshonok, 1997 .

Overexpression of a bacterial chymotrypsin: application for L-amino acid ester hydrolysis.

L. Pollegioni, S. Servi, P. D’Arrigo, 2011, Enzyme and microbial technology.

Fast atom bombardment and angle resolved mass spectrometry in the structural and stereochemical characterization of homochiral 3‐deoxy‐3‐fluoro muscarins

P. Traldi, F. Viani, P. Bravo, 1991 .

Naphthyl-l-α-amino acids via chemo-enzymatic dynamic kinetic resolution

S. Servi, Davide Tessaro, P. D’Arrigo, 2012 .

Dimerizable Redox‐Sensitive Triazine‐Based Cationic Lipids for in vitro Gene Delivery

N. Zaffaroni, C. Verpelli, C. Sala, 2007, ChemMedChem.

Synthesis of Enantiomerically Pure 3′-Arylsulfonyl-4′-fluoromethyl-4′-(diethoxyphosphorylmethyl)thymidine Analogues

A. Arnone, C. Zappalà, M. Frigerio, 1997 .

Peptidyl fluoro-ketones as proteolytic enzyme inhibitors.

R. Sinisi, F. Viani, M. Sani, 2006, Current topics in medicinal chemistry.

Fluorinated Barbituric Acid Derivatives: Synthesis and Bio-activity

M. Zanda, F. Viani, L. Bruché, 2003 .

Design of a novel LOX-1 receptor antagonist mimicking the natural substrate.

P. Patrizi, A. Desideri, M. Falconi, 2013, Biochemical and biophysical research communications.

Enzyme oxidation of plant galactomannans yielding biomaterials with novel properties and applications, including as delivery systems

T. Silvetti, M. Brasca, P. Campia, 2018, Applied Microbiology and Biotechnology.

SYNTHESIS OF BOTH ANANTIOMERS OF ALPHA -(TRIFLUOROMETHYL)BUTYRINE AND ALPHA -(TRIFLUOROMETHYL)PHENYLALANINE

M. Zanda, O. Shishkin, Y. Struchkov, 1996 .