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2016

A Mesoionic Carbene as Neutral Ligand for Phosphorescent Cationic Ir(III) Complexes

A Mesoionic Carbene as Neutral Ligand for Phosphorescent Cationic Ir(III) Complexes

 

A. Baschieri, F. Monti, E. Matteucci, A. Mazzanti, A. Barbieri, N. Armaroli, L. Sambri

Inorg. Chem. 2016, 55, 7912−7919

https://doi.org/10.1021/acs.inorgchem.6b00869

An Atropisomerically Enforced Phosphoric Acid forOrganocatalytic Asymmetric Reactions

An Atropisomerically Enforced Phosphoric Acid forOrganocatalytic Asymmetric Reactions

 

L. Bernardi, G. Bolzoni, M. Fochi, M. Mancinelli, A. Mazzanti

Eur. J. Org. Chem. 2016, 3208–3216

https://doi.org/10.1002/ejoc.201600296

Atropisomerism in 3-arylthiazolidine-2-thiones. A combined dynamic NMR and dynamic HPLC study

Atropisomerism in 3-arylthiazolidine-2-thiones. A combined dynamic NMR and dynamic HPLC study

 

A. Ciogli, S. Vivek Kumar, M. Mancinelli, A. Mazzanti, S. Perumal, C. Severi, C. Villani

Org. Biomol. Chem., 2016, 14, 11137

https://doi.org/10.1039/C6OB02145J

Axial Chirality about Boron–Carbon Bond: Atropisomeric Azaborines

Axial Chirality about Boron–Carbon Bond: Atropisomeric Azaborines

 

A. Mazzanti, E. Mercanti, M. Mancinelli

Org. Lett. 2016, 18, 2692−2695

https://doi.org/10.1021/acs.orglett.6b01159

Catalytic Enantioselective Addition of Indoles to Activated N‑Benzylpyridinium Salts: Nucleophilic Dearomatization of Pyridines with Unusual C‑4 Regioselectivity

Catalytic Enantioselective Addition of Indoles to Activated N‑Benzylpyridinium Salts: Nucleophilic Dearomatization of Pyridines with Unusual C‑4 Regioselectivity

 

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

ACS Catal. 2016, 6, 6473−6477

https://doi.org/10.1021/acscatal.6b01962

Computational and DNMR Analysis of the Conformational Isomers and Stereodynamics of Secondary 2,2′-Bisanilides

Computational and DNMR Analysis of the Conformational Isomers and Stereodynamics of Secondary 2,2′-Bisanilides

 

A. Mazzanti, M. Chiarucci, L. Prati, K. W. Bentley, C. Wolf

J. Org. Chem. 2016, 81, 89−99

https://doi.org/10.1021/acs.joc.5b02330

Enantioselective Organocatalytic Cyclopropanation of Enals Using Benzyl Chlorides

Enantioselective Organocatalytic Cyclopropanation of Enals Using Benzyl Chlorides

 

M. Meazza, M. Ashe, H. Y. Shin, H. S. Yang, A. Mazzanti, J. W. Yang, R. Rios

J. Org. Chem. 2016, 81, 3488−3500

https://doi.org/10.1021/acs.joc.5b02801

New azo-decorated N-pyrrolidinylthiazoles: synthesis, properties and an unexpected remote substituent effect transmission

New azo-decorated N-pyrrolidinylthiazoles: synthesis, properties and an unexpected remote substituent effect transmission

 

C. Boga, S. Cino, G. Micheletti, D. Padovan, L. Prati, A. Mazzanti, N. Zanna

Org. Biomol. Chem., 2016, 14, 7061-7068

https://doi.org/10.1039/C6OB00994H

Straightforward synthesis of a novel ring-fused pyrazole-lactam andin vitro cytotoxic activity on cancer cell lines

Straightforward synthesis of a novel ring-fused pyrazole-lactam andin vitro cytotoxic activity on cancer cell lines

 

G. Bertuzzi, E. Locatelli, D. Colecchia, P. Calandro, B.F. Bonini, J.Z. Chandanshive, A. Mazzanti, P. Zani, M. Chiariello, M. Comes Franchini

European Journal of Medicinal Chemistry 2016, 117, 1-7

https://doi.org/10.1016/j.ejmech.2016.04.006

Synergistic formal ring contraction for the enantioselective synthesis of spiropyrazolones

Synergistic formal ring contraction for the enantioselective synthesis of spiropyrazolones

 

M. Meazza, M. Kamlar, L. Jašíková,  Bedřich Formánek, A. Mazzanti, Jana Roithová, Jan Veselý, R. Rios

Chem. Sci., 2018, 9, 6368-6373

https://doi.org/10.1039/C8SC00913A

Targeting remote axial chirality control ofN-(2-tert-butylphenyl)succinimides by means of Michael addition type reactions

Targeting remote axial chirality control ofN-(2-tert-butylphenyl)succinimides by means of Michael addition type reactions

 

N. Di Iorio, F. Champavert, A. Erice, P. Righi, A. Mazzanti, G. Bencivenni

Tetrahedron 2016, 72, 5191-5201

https://doi.org/10.1016/j.tet.2016.02.052

Reversible modulation of the activity of thiourea catalysts with anions: a simple approach to switchable asymmetric catalysis

Reversible modulation of the activity of thiourea catalysts with anions: a simple approach to switchable asymmetric catalysis

Giacomo Foli, Cecilia Sasso D’Elia, Mariafrancesca Fochi and Luca Bernardi

RSC Adv. 2016, 6, 66490-66494

https://pubs.rsc.org/en/content/articlelanding/2016/ra/c6ra12732k/unauth#!divAbstract

A General Catalytic Enantioselective Transfer Hydrogenation Reaction of β,β-Disubstituted Nitroalkenes Promoted by a Simple Organocatalyst

A General Catalytic Enantioselective Transfer Hydrogenation Reaction of β,β-Disubstituted Nitroalkenes Promoted by a Simple Organocatalyst

 

Luca Bernardi and Mariafrancesca Fochi


Molecules 2016 vol. 21 (8) Article number 1000 pp.1-14

OPEN ACCESS

 https://doi.org/10.3390/molecules21081000

Organocatalytic Enantioselective Transfer Hydrogenation of -Amino Nitroolefins

Organocatalytic Enantioselective Transfer Hydrogenation of b-Amino Nitroolefins

 

Antonino Ferraro, Luca Bernardi and Mariafrancesca Fochi

Adv. Synth. Catal. 2016, 358, 1561 – 1565

https://doi.org/10.1002/adsc.201600061

Synthesis and Preliminary Results on the Catalytic Activity of Metal Complexes obtained from C2‐Symmetric Ligands Derived from R‐(+)‐Betti base

Synthesis and Preliminary Results on the Catalytic Activity of Metal Complexes obtained from C2‐Symmetric Ligands Derived from R‐(+)‐Betti base

 

T. Rigotti, P. Righi, E. Marotta, C. Paolucci

Chemsitry SELECT 2016, 1, 2624 - 2629

 https://doi.org/10.1002/slct.201600547