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2017

Anionic Cyclometalated Iridium(III) Complexes with a Bis-Tetrazolate Ancillary Ligand for Light-Emitting Electrochemical Cells

Anionic Cyclometalated Iridium(III) Complexes with a Bis-Tetrazolate Ancillary Ligand for Light-Emitting Electrochemical Cells

 

E. Matteucci, A. Baschieri, A. Mazzanti, L. Sambri, J. Ávila, A. Pertegás, H. J. Bolink, F. Monti, E. Leoni, N. Armaroli

Inorg. Chem. 2017, 56, 10584−10595

https://doi.org/10.1021/acs.inorgchem.7b01544

Betti’s base for crystallization-induced deracemization of substituted aldehydes: synthesis of enantiopure amorolfine and fenpropimorph

Betti’s base for crystallization-induced deracemization of substituted aldehydes: synthesis of enantiopure amorolfine and fenpropimorph

 

A. Carella, G. R. Ferronatto, E. Marotta, A. Mazzanti, P. Righi, C. Paolucci

Org. Biomol. Chem., 2017, 15, 2968

https://doi.org/10.1039/C6OB02765B

Conformational Analysis and Absolute Configuration of Axially Chiral 1‑Aryl and 1,3-Bisaryl-xanthines

Conformational Analysis and Absolute Configuration of Axially Chiral 1‑Aryl and 1,3-Bisaryl-xanthines

 

M. Mancinelli, S. Perticarari, L. Prati, A. Mazzanti

J. Org. Chem. 2017, 82, 6874−6885

https://doi.org/10.1021/acs.joc.7b01010

Controlling the C(sp3)−C(sp2) Axial Conformation in the Enantioselective Friedel−Crafts-Type Alkylation of β‑Naphthols with Inden-1-ones

Controlling the C(sp3)−C(sp2) Axial Conformation in the Enantioselective Friedel−Crafts-Type Alkylation of β‑Naphthols with Inden-1-ones

 

N. Di Iorio, G. Filippini, A. Mazzanti, P. Righi, G. Bencivenni

Org. Lett. 2017, 19, 6692−6695

https://doi.org/10.1021/acs.orglett.7b03415

Highly Enantioselective Synthesis of Alkylpyridine Derivativesthrough a Michael/Michael/Aldol Cascade Reaction

Highly Enantioselective Synthesis of Alkylpyridine Derivativesthrough a Michael/Michael/Aldol Cascade Reaction

 

M. Meazza, M. Potter, M. B. Pitak, S. J. Coles, A. Mazzanti, R. Rios

Eur. J. Org. Chem. 2017, 719–725

https://doi.org/10.1002/ejoc.201601491

Hydroxy‐ and Methoxybenzene Derivatives with Benzenediazonium Salts ― Chemical Behavior and Tautomeric Problems

Hydroxy‐ and Methoxybenzene Derivatives with Benzenediazonium Salts ― Chemical Behavior and Tautomeric Problems

 

G. Micheletti, C. Boga, L. Forlani, E. Del Vecchio, N. Zanna, A. Mazzanti, M. Monari

Eur. J. Org. Chem. 2017, 964–974

https://doi.org/10.1002/ejoc.201601393

Michael Addition of Oxindoles to N-(2-tert-Butylphenyl)maleimides: Efficient Desymmetrization for the Synthesis of Atropisomeric Succinimides with Quaternary and Tertiary Stereocenters

Michael Addition of Oxindoles to N-(2-tert-Butylphenyl)maleimides: Efficient Desymmetrization for the Synthesis of Atropisomeric Succinimides with Quaternary and Tertiary Stereocenters

 

N. Di Iorio, L. Soprani, S. Crotti, E. Marotta, A. Mazzanti, P. Righi, G. Bencivenni

Synthesis 2017, 49, 1519–1530

http://dx.doi.org/10.1055/s-0036-1588408

N-heterocyclic linkers from 1,2-diaza-1,3-dienes for dye-sensitizedsolar cells: DFT calculations, synthesis and photovoltaic performance

N-heterocyclic linkers from 1,2-diaza-1,3-dienes for dye-sensitizedsolar cells: DFT calculations, synthesis and photovoltaic performance

 

A. Fattori, R. Majer, A. Mazzanti, M. F. Ottaviani, A. Modelli, F. Mantellini, S. Santeusanio

Dyes and Pigments 2017, 145, 246-255

https://doi.org/10.1016/j.dyepig.2017.05.058

Nucleophilic Dearomatization of Pyridines under Enamine Catalysis: Regio-, Diastereo-, and Enantioselective Addition of Aldehydes to Activated N-Alkylpyridinium Salts

Nucleophilic Dearomatization of Pyridines under Enamine Catalysis: Regio-, Diastereo-, and Enantioselective Addition of Aldehydes to Activated N-Alkylpyridinium Salts

 

G. Bertuzzi, A. Sinisi, D. Pecorari, L. Caruana, A. Mazzanti, L. Bernardi, M. Fochi

Org. Lett. 2017, 19, 834−837

https://doi.org/10.1021/acs.orglett.6b03824

Organocatalytic Asymmetric Sulfa‐Michael Addition of 2‐Aminothiophenols to Chalcones: First Enantioselective Access to 2,3,4,5‐Tetrahydro‐1,5‐benzothiazepines

Organocatalytic Asymmetric Sulfa‐Michael Addition of 2‐Aminothiophenols to Chalcones: First Enantioselective Access to 2,3,4,5‐Tetrahydro‐1,5‐benzothiazepines

 

V. Corti, P. Camarero Gonzalez, J. Febvay, L. Caruana, A. Mazzanti, M. Fochi, L. Bernardi

Eur. J. Org. Chem. 2017, 49–52

 https://doi.org/10.1002/ejoc.201601364

Synthesis and investigation on processing-depending polarized fluorescence emission in thin-films of 2,2′-([2,2′-bithiophene]-5,5′-diyl)bis(5-octyl-4-phenyl-4H-thieno[2,3-c]pyrrol-6(5H)-one)

Synthesis and investigation on processing-depending polarized fluorescence emission in thin-films of 2,2′-([2,2′-bithiophene]-5,5′-diyl)bis(5-octyl-4-phenyl-4H-thieno[2,3-c]pyrrol-6(5H)-one)

 

L. Favaretto, M. Zambianchi, S. G. Lopez, A. Mazzanti, C. Zanardi, R. Seeber, D. Gentili, F. Valle, E. Benvenuti, M. Muccini, G. Ruani, F. Mercuri, S. Milita, F. Liscio, M. Cavallini, S. Toffanin, M. Melucci

J. Mater. Chem. C, 2017, 5, 10320

 https://doi.org/10.1039/c7tc03930a

Tetrasubstituted cyclopentadienones as suitable enantiopure ligands with axial chirality

Tetrasubstituted cyclopentadienones as suitable enantiopure ligands with axial chirality

 

L. Prati, M. Mancinelli, A. Ciogli, A. Mazzanti

Org. Biomol. Chem., 2017, 15, 8720

https://doi.org/10.1039/C7OB01455D

3,5-Dinitrobenzoyl-9-amino-9-deoxy-9-epiquinine as Pirkle-Anion Exchange Hybrid-Type Chiral Selector in High-Performance Liquid Chromatography

3,5-Dinitrobenzoyl-9-amino-9-deoxy-9-epiquinine as Pirkle-Anion Exchange Hybrid-Type Chiral Selector in High-Performance Liquid Chromatography

 

M. De Martino, G. Bencivenni, A. Mazzanti, S. Menta, O. H. Ismail, R. Sabia, A. Ciogli

Chromatographia 2017, 80, 751–762

https://doi.org/10.1007/s10337-016-3161-6

Enantioselective Approaches to 3,4-Annulated Indoles Using Organocatalytic Domino Reactions

Enantioselective Approaches to 3,4-Annulated Indoles Using Organocatalytic Domino Reactions

Lorenzo Caruana, Mariafrancesca Fochi and Luca Bernardi

Synlett 2017, 28, 1530–1543

https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0036-1589494