S. Superchi

发表

Determination of absolute configuration using vibrational circular dichroism spectroscopy: the chiral sulfoxide 1-thiochromanone S-oxide.

P. Stephens, F. Devlin, C. Rosini, 2002, Chirality.

Amplification of the chiroptical response of UV-transparent amines and alcohols by N-phthalimide derivatization enabling absolute configuration determination through ECD computational analysis.

G. Mazzeo, Daniele Padula, P. Scafato, 2020, Organic & biomolecular chemistry.

Capillary electrophoretic resolution of chiral aryl alkyl and aryl benzyl sulphoxides using sulphated β‐cyclodextrins as chiral selectors

C. Rosini, S. Superchi, A. J. Hutt, 2001 .

New Isoflavonoids from the extract of Rhynchosia precatoria (Humb. & Bonpl. ex Willd.) DC. and their antimycobacterial activity.

M. Curini, S. Superchi, A. Garibay-Escobar, 2017, Journal of ethnopharmacology.

Absolute Configuration Assignment to Chiral Natural Products by Biphenyl Chiroptical Probes: The Case of the Phytotoxins Colletochlorin A and Agropyrenol

M. Masi, A. Evidente, P. Scafato, 2020, Journal of natural products.

Absolute Configuration Assignment from Optical Rotation Data by Means of Biphenyl Chiroptical Probes.

P. Scafato, S. Superchi, S. Belviso, 2019, Chemistry.

Central-to-axial chirality induction in biphenyl chiroptical probes for the stereochemical characterization of chiral primary amines.

P. Scafato, S. Superchi, S. Vergura, 2018, Organic & biomolecular chemistry.

Helical Sense-Responsive and Substituent-Sensitive Features in Vibrational and Electronic Circular Dichroism, in Circularly Polarized Luminescence, and in Raman Spectra of Some Simple Optically Active Hexahelicenes

A. Mele, M. Tommasini, C. Villani, 2014 .

Thioethyl‐Porphyrazine/Nanocarbon Hybrids for Photoinduced Electron Transfer

S. Bellani, F. Bonaccorso, A. E. D. R. Castillo, 2018, 1903.08944.

Absolute Configuration Sensing of Chiral Aryl- and Aryloxy-Propionic Acids by Biphenyl Chiroptical Probes

S. Orlando, P. Scafato, S. Superchi, 2021, Chemosensors.

Diplofuranoxin, a disubstituted dihydrofuranone, was produced together with sphaeropsidin A and epi-sphaeropsidone by Diplodia subglobosa, an emerging ash (Fraxinus excelsior L.) pathogen in Europe.

M. Masi, A. Evidente, B. T. Linaldeddu, 2022, Phytochemistry.

Further secondary metabolites produced by the fungus Pyricularia grisea isolated from buffelgrass (Cenchrus ciliaris).

M. Masi, A. Evidente, S. Meyer, 2020, Chirality.

Drophiobiolins A and B, Bioactive Ophiobolan Sestertepenoids Produced by Dreschslera gigantea.

V. Calabrò, M. Masi, A. Evidente, 2020, Journal of natural products.

Stoechanones A and B, Phytotoxic Copaane Sesquiterpenoids Isolated from Lavandula stoechas with Potential Herbicidal Activity against Amaranthus retroflexus.

M. Masi, A. Evidente, S. Superchi, 2020, Journal of natural products.

Assignment Through Chiroptical Methods of The Absolute Configuration of Fungal Dihydropyranpyran-4-5-Diones Phytotoxins, Potential Herbicides for Buffelgrass (Cenchrus ciliaris) Biocontrol

M. Masi, A. Evidente, G. Mazzeo, 2019, Molecules.

α-Costic acid, a plant sesquiterpene with acaricidal activity against Varroa destructor parasitizing the honey bee

A. Cimmino, M. Masi, A. Evidente, 2019, Natural product research.

Absolute configuration assignment to anticancer Amaryllidaceae alkaloid jonquailine.

M. Masi, A. Evidente, G. Mazzeo, 2018, Fitoterapia.

Chenopodolans E and F, two new furopyrans produced by Phoma chenopodiicola and absolute configuration determination of chenopodolan B

A. Cimmino, M. Masi, A. Evidente, 2016 .

Phytotoxins produced by Phoma chenopodiicola, a fungal pathogen of Chenopodium album.

A. Cimmino, M. Masi, A. Evidente, 2015, Phytochemistry.

Cationic half-sandwich quinolinophaneoxazoline-based (η6-p-cymene)ruthenium(II) complexes exhibiting different chirality types: synthesis and structural determination by complementary spectroscopic methods.

S. Lepri, G. Bellachioma, G. Ciancaleoni, 2014, Dalton transactions.

Enantiopure Dendrimers Derived from the 1,1′-Binaphthyl Moiety: A Correlation Between Chiroptical Properties and Conformation of the 1,1′-Binaphthyl Template

C. Rosini, S. Superchi, H. Peerlings, 2000 .

1,1′-Binaphthylazepine-based ligands for the enantioselective dialkylzinc addition to aromatic aldehydes

S. Superchi, L. Pisani, 2008 .

Synthetic approach toward cis-disubstituted γ- and δ-lactones through enantioselective dialkylzinc addition to aldehydes: application to the synthesis of optically active flavors and fragrances

C. Rosini, P. Scafato, S. Superchi, 2012 .

Enantioselective alkynylation and phenylation of aromatic aldehydes promoted by atropisomeric 1,1′-binaphthylazepine-based amino alcohols

S. Superchi, M. Pizzuti, 2005 .

Rational design of chiral 1,1′-binaphthylazepine-based ligands for the enantioselective addition of ZnEt2 to aromatic aldehydes

E. Giorgio, C. Rosini, P. Scafato, 2002 .

Chirality Transfer in a Calixarene-Based Directional Pseudorotaxane Complex

C. Gaeta, P. Neri, S. Superchi, 2021, Chemistry.

Fungal phytotoxins with potential herbicidal activity: chemical and biological characterization.

A. Cimmino, M. Masi, A. Evidente, 2015, Natural product reports.

Catalytic Asymmetric Oxidation of Aryl Sulfides with a Ti/H2O/(R,R)-Diphenylethane-1,2-diol Complex: a Versatile and Highly Enantioselective Oxidation Protocol

C. Rosini, S. Superchi, M. I. Donnoli, 1998 .

Mitochondrial Role in Intrinsic Apoptosis Induced by a New Synthesized Chalcone in Hepatocellular Carcinoma Cells

Isabella Pisano, P. Convertini, A. Santarsiero, 2022, Biomedicines.

In Vitro Effects of Fungal Phytotoxins on Cancer Cell Viability: First Insight into Structure Activity Relationship of a Potent Metabolite of Cochliobolus australiensis Radicinin

A. Kornienko, V. Mathieu, M. Masi, 2022, Toxins.

Porphyrins Through the Looking Glass: Spectroscopic and Mechanistic Insights in Supramolecular Chirogenesis of New Self-Assembled Porphyrin Derivatives

R. Paolesse, G. Magna, C. Di Natale, 2020, Frontiers in Chemistry.

Towards a correlation of absolute configuration and chiroptical properties of alkyl aryl sulfoxides: a coupled-oscillator foundation of the empirical Mislow rule?

C. Rosini, S. Superchi, M. I. Donnoli, 2001, Chemistry.

Synthetic Approach Toward cis-Disubstituted γ- and δ-Lactones Through Enantioselective Dialkylzinc Addition to Aldehydes: Application to the Synthesis of Optically Active Flavors and Fragrances.

C. Rosini, P. Scafato, S. Superchi, 2012 .

Absolute Configuration Determination by Quantum Mechanical Calculation of Chiroptical Spectra: Basics and Applications to Fungal Metabolites.

G. Pescitelli, M. Górecki, P. Scafato, 2018, Current medicinal chemistry.

Synthesis and Herbicidal Activity Against Buffelgrass (Cenchrus ciliaris) of (±)-3-deoxyradicinin

M. Masi, A. Evidente, M. Cristofaro, 2019, Molecules.

An umpolung sulfoxide reagent for use as a functionalized benzyl carbanion equivalent

G. Pinna, A. Volonterio, M. Zanda, 2011 .

Circular dichroism spectra and absolute configuration of some aryl methyl sulfoxides.

E. Giorgio, C. Rosini, S. Superchi, 2003, Organic & biomolecular chemistry.

Determination of absolute configuration using vibrational circular dichroism spectroscopy: the chiral sulfoxide 1-thiochroman S-oxide

P. Stephens, F. Devlin, C. Rosini, 2001 .

Computational ECD spectrum simulation of the phytotoxin scytalone: importance of solvent effects on conformer populations.

A. Cimmino, A. Evidente, G. Mazzeo, 2014, Chirality.

Anomalous Face-Selectivity in Sharpless Asymmetric Dihydroxylation of o-Allylbenzamides.

F. Minutolo, P. Salvadori, S. Superchi, 1996, The Journal of organic chemistry.

5,5,7,7-Tetrametyl-6,7-dihydro-5H-dibenzo[c,e]azepine

P. Scafato, S. Superchi, D. Casarini, 2023, Molbank.

Synthesis and toxicity to mammalian cells of the carrot dihydroisocoumarins.

F. Marinelli, U. Zanelli, P. Salvadori, 1993, Chemical research in toxicology.

Asymmetric Synthesis of the Dihydroisocoumarin Moiety of AI-77-B via Copper-Mediated Cross-Coupling and Sharpless Asymmetric Dihydroxylation.

F. Minutolo, P. Salvadori, S. Superchi, 1996, The Journal of organic chemistry.

Asymmetric addition of dimethylzinc to alkylidenmalonates mediated by phosphorous ligands: a new synthetic route to floral fragrances.

P. Scafato, S. Superchi, L. Pisani, 2011, Chirality.

Synthesis and Stereochemical Characterization of a Novel Chiral α-Tetrazole Binaphthylazepine Organocatalyst

G. Longhi, S. Abbate, P. Scafato, 2022, Molecules.

Enantioselective synthesis of the fragrance trans-magnolione under asymmetric phase transfer catalysis

C. Rosini, P. Scafato, S. Superchi, 2005 .

Enantiopure p,p′-disubstituted 1,2-diphenylethane-1,2-diols as chiral inducers in the Ti-mediated oxidation of sulfides: a case of reversal of asymmetric induction by fluorine substitution

C. Rosini, S. Superchi, M. I. Donnoli, 1998 .

1,1′-Binaphthylazepine-based ligands for asymmetric catalysis. Part 2: New aminoalcohols as chiral ligands in the enantioselective addition of ZnEt2 to aromatic aldehydes

E. Giorgio, C. Rosini, S. Superchi, 2001 .

Enantioselective oxidation of sulfides catalyzed by titanium complexes of 1,2-diarylethane-1,2-diols: effect of the aryl substitution.

C. Rosini, P. Scafato, S. Superchi, 2008, Chirality.

1,1′-Binaphthylazepine-based ligands for asymmetric catalysis. Part 1: Preparation and characterization of some new aminoalcohols and diamines

E. Giorgio, C. Rosini, S. Superchi, 2001 .

Determination of Molecular Absolute Configuration: Guidelines for Selecting a Suitable Chiroptical Approach

E. Giorgio, C. Rosini, G. Mazzeo, 2012 .

Amaryllidaceae alkaloids: Absolute configuration and biological activity.

A. Cimmino, M. Masi, A. Evidente, 2017, Chirality.

Induction of a Preferred Twist in a Biphenyl Core by Stereogenic Centers: A Novel Approach to the Absolute Configuration of 1,2- and 1,3-Diols.

C. Rosini, A. Bavoso, A. Laurita, 2001, Angewandte Chemie.

Absolute configurations of phytotoxic inuloxins B and C based on experimental and computational analysis of chiroptical properties.

Ana G. Petrovic, N. Berova, A. Cimmino, 2016, Phytochemistry.

Regiolone and Isosclerone, Two Enantiomeric Phytotoxic Naphthalenone Pentaketides: Computational Assignment of Absolute Configuration and Its Relationship with Phytotoxic Activity

D. Rubiales, A. Cimmino, A. Evidente, 2011 .

Synthesis and stereochemical characterization of optically active 1,2-diarylethane-1,2-diols: useful chiral controllers in the Ti-mediated enantioselective sulfoxidation.

C. Rosini, P. Scafato, S. Superchi, 2001, Chirality.

Circular dichroism spectra (350–185 nm) of a new series of 4-substituted [2.2]paracyclophanes: A quantitative analysis within the DeVoe polarizability model

C. Rosini, O. Piermatti, S. Superchi, 1998 .

The absolute configuration of simple aliphatic alcohols through a chemical/computational approach: triarylether derivatives of (+)-endo-2-norborneol as a case study

C. Rosini, G. Mazzeo, P. Scafato, 2009 .

Asymmetric synthesis and structure-activity studies of the fungal metabolites colletorin A, colletochlorin A and their halogenates analogues

J. Bloomquist, M. Masi, A. Evidente, 2018, Tetrahedron.

Anomalous Face‐Selectivity in Sharpless Asymmetric Dihydroxylation of o‐Allylbenzamides.

F. Minutolo, P. Salvadori, S. Superchi, 1996 .

Selective and Practical Oxidation of Sulfides to Diastereopure Sulfoxides: A Combined Experimental and Computational Investigation

B. Cosimelli, D. Spinelli, A. Ciogli, 2013 .

Monobenzylethers of (R, R)-1,2-diphenylethane-1,2-diol as a possible alternative to cyclohexyl-based chiral auxiliaries in the stereoselective reduction of α-ketoesters

C. Rosini, P. Scafato, S. Superchi, 2002 .

Tropos Amino Alcohol Mediated Enantioselective Aryl Transfer Reactions to Aromatic Aldehydes

P. Scafato, S. Superchi, L. Pisani, 2014 .

Monobenzylether of (R,R)-1,2-diphenylethane-1,2-diol as chiral auxiliary in the diastereoselective reduction of α-ketoesters

C. Rosini, S. Superchi, M. Contursi, 1998 .

Asymmetric Synthesis of the Dihydroisocoumarin Moiety of AI-77-B via Copper-Mediated Cross-Coupling and Sharpless Asymmetric Dihydroxylation.

F. Minutolo, P. Salvadori, S. Superchi, 1996, The Journal of organic chemistry.

Synthesis, enzymatic resolution, and stereochemical characterization of isoparaconic acid derivatives: a combined experimental and theoretical investigation.

G. Mazzeo, S. Superchi, F. Felluga, 2014, Chirality.

Noncovalent organocatalysis: a powerful tool for the nucleophilic epoxidation of α-ylideneoxindoles.

G. Mazzeo, T. Gasperi, D. Tofani, 2011, Organic letters.

Computational Approaches and Use of Chiroptical Probes in the Absolute Configuration Assignment to Natural Products by ECD Spectroscopy: A 1,2,3-Trihydroxy-p-menthane as a Case Study

A. Evidente, P. Scafato, S. Superchi, 2022, Biomolecules.

α-Aryl O-vinyl carbamates. Tandem carbolithiation — α-alkylation and -[1,2]-Wittig rearrangement reactions

N. Sotomayor, V. Snieckus, S. Superchi, 1996 .

Regio- and stereoselective intermolecular carbolithiation reactions

P. Scafato, S. Superchi, S. Belviso, 2020, RSC advances.

Central-to-axial chirality transfer revealed by liquid crystals: a combined experimental and computational approach for the determination of absolute configuration of carboxylic acids with an α chirality centre.

C. Rosini, A. Ferrarini, G. Spada, 2011, Chirality.

Flexible biphenyl chromophore as a circular dichroism probe for assignment of the absolute configuration of carboxylic acids.

C. Rosini, A. Laurita, S. Superchi, 2006, Journal of the American Chemical Society.

Determination of absolute configuration using vibrational circular dichroism spectroscopy: the chiral sulfoxide 1-(2-methylnaphthyl) methyl sulfoxide.

P. Stephens, F. Devlin, C. Rosini, 2001, The Journal of organic chemistry.

Synthesis and L-type calcium channel blocking activity of new chiral oxadiazolothiazinones.

B. Cosimelli, F. Devlin, E. Carosati, 2015, European journal of medicinal chemistry.

Structural determinations by circular dichroism spectra analysis using coupled oscillator methods: an update of the applications of the DeVoe polarizability model.

Carlo Rosini, Stefano Superchi, E. Giorgio, 2004, Chirality.

Absolute configurations of fungal and plant metabolites by chiroptical methods. ORD, ECD, and VCD studies on phyllostin, scytolide, and oxysporone.

Ana G. Petrovic, N. Berova, A. Cimmino, 2013, Journal of natural products.

Application of Mosher's method for absolute configuration assignment to bioactive plants and fungi metabolites

A. Cimmino, M. Masi, A. Evidente, 2017, Journal of pharmaceutical and biomedical analysis.

Stereochemical Stability and Absolute Configuration of Atropisomeric Alkylthioporphyrazines by Dynamic NMR and HPLC Studies and Computational Analysis of HPLC-ECD Recorded Spectra

F. Lelj, C. Villani, S. Superchi, 2018, European Journal of Organic Chemistry.

Electrical and mechanical anharmonicities from NIR-VCD spectra of compounds exhibiting axial and planar chirality: the cases of (S)-2,3-pentadiene and methyl-d(3) (R)- and (S)-[2.2]paracyclophane-4-carboxylate.

G. Longhi, S. Abbate, F. Gangemi, 2011, Chirality.

Determination of the Absolute Configuration of 1-Arylethane-1,2-diols by a Nonempirical Analysis of the CD Spectra of Their 4-Biphenylboronates

C. Rosini, S. Superchi, and Maria Irene Donnoli, 1999 .

Absolute configurations of phytotoxins seiricardine A and inuloxin A obtained by chiroptical studies.

Ana G. Petrovic, N. Berova, A. Cimmino, 2015, Phytochemistry.

A correlation between the absolute configuration of alkyl aryl sulfoxides and their helical twisting powers in nematic liquid crystals.

C. Rosini, G. Gottarelli, A. Ferrarini, 2003, The Journal of organic chemistry.

Absolute configuration of bioactive furanogermacrenones from Commiphora erythraea (Ehrenb) Engl. by computational analysis of their chiroptical properties

S. Superchi, E. Santoro, M. Marcotullio, 2014 .

Argyrotoxins A-C, a trisubstituted dihydroisobenzofuranone, a tetrasubstituted 2-hydroxyethylbenzamide and a tetrasubstitutedphenyl trisubstitutedbutyl ether produced by Alternaria argyroxiphii, the causal agent of leaf spot on African mahogany trees (Khaya senegalensis).

M. Masi, A. Evidente, L. Maddau, 2021, Phytochemistry.

Pinofuranoxins A and B, Bioactive Trisubstituted Furanones Produced by the Invasive Pathogen Diplodia sapinea

M. Masi, A. Evidente, B. T. Linaldeddu, 2021, Journal of Natural Products.

Structure and Absolute Configuration of Kongiidiazadione, a New Phytotoxic 3-Substituted-5-Diazenylcyclopentendione Produced by Diaporthe Kongii.

G. Ash, A. Cimmino, A. Evidente, 2015, Chirality.

Absolute configurations of chiral molecules with multiple stereogenic centers without prior knowledge of the relative configurations: A case study of inuloxin C.

Ana G. Petrovic, N. Berova, A. Cimmino, 2018, Chirality.

Agarsenone, a Cadinane Sesquiterpenoid from Commiphora erythraea.

S. Superchi, E. Santoro, C. Santi, 2013, Journal of natural products.

Papyracillic acid, a phytotoxic 1,6-dioxaspiro[4,4]nonene produced by Ascochyta agropyrina Var. nana, a potential mycoherbicide for Elytrigia repens biocontrol.

A. Cimmino, A. Evidente, A. Andolfi, 2009, Journal of agricultural and food chemistry.

Synthesis and absolute configuration of a new chiral [2.2]paracyclophane-based diene

C. Rosini, Daniela Lanari, A. Marrocchi, 2002 .

α-Zinc >O-vinyl carbamates as anionic Friedel-Crafts equivalents. Cross coupling reactions with aryl and heteroaryl halides and triflates

N. Sotomayor, V. Snieckus, S. Superchi, 1996 .

Natural and Synthetic Furanones with Anticancer Activity

R. Kiss, V. Mathieu, A. Cimmino, 2016, Natural product communications.

Catalytic asymmetric oxidation of aryl methyl sulfides mediated by a (S,S)-1,2-diphenylethan-1,2-diol/titanium/water complex

C. Rosini, S. Superchi, 1997 .

Biphenyl dioxolanes as circular dichroism probes for the assignment of absolute configuration to aliphatic diols: Extending the scope to anti 1,n-diols and cyclic syn 1,2-diols.

P. Scafato, S. Superchi, 2010, Chirality.