vai al contenuto della pagina vai al menu di navigazione

2015

A chelating diisocyanide ligand for cyclometalated Ir(III) complexes with strong and tunable luminescence

A chelating diisocyanide ligand for cyclometalated Ir(III) complexes with strong and tunable luminescence

 

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

Faraday Discuss., 2015, 185, 233-248

https://doi.org/10.1039/C5FD00064E

An Unexpected Pathway to Enantiomerization of Hemithioketals in TolueneInvolving a Dimeric Transition State: A Combined Experimental andComputational Study

An Unexpected Pathway to Enantiomerization of Hemithioketals in TolueneInvolving a Dimeric Transition State: A Combined Experimental andComputational Study

 

A. Bottoni, M. Calvaresi, B. Cosimelli, A. Mazzanti, M. Rambaldi, D. Spinelli

Eur. J. Org. Chem. 2015, 4353–4357

 https://doi.org/10.1002/ejoc.201500421

APTES mediated modular modification of regenerated silk fibroin in a water solution

APTES mediated modular modification of regenerated silk fibroin in a water solution

 

A. Sagnella, M. Zambianchi, M. Durso, T. Posati, A. Del Rio, A. Donnadio, A. Mazzanti, A. Pistone, G. Ruani, R. Zamboni, V. Benfenati, M. Melucci

RSC Adv., 2015, 5, 63401-53406

https://doi.org/10.1039/C5RA10016J

Catalytic Asymmetric Addition of Meldrum’sAcid, Malononitrile,and 1,3-Dicarbonyls to ortho-Quinone Methides Generated In SituUnder Basic Conditions

Catalytic Asymmetric Addition of Meldrum’sAcid, Malononitrile,and 1,3-Dicarbonyls to ortho-Quinone Methides Generated In SituUnder Basic Conditions

 

L. Caruana, M. Mondatori, V. Corti, S. Morales, A. Mazzanti, M. Fochi, L. Bernardi

Chem. Eur.J. 2015, 21, 6037 –6041

https://doi.org/10.1002/chem.201500710

Catalytic Asymmetric Reactions of 4-Substituted IndoleswithNitroethene:ADirect EntrytoErgot Alkaloid Structures

Catalytic Asymmetric Reactions of 4-Substituted Indoles with Nitroethene: A Direct Entry to Ergot Alkaloid Structures

 

S. Romanini, E. Galletti, L. Caruana, A. Mazzanti, F. Himo, S. Santoro, M. Fochi, L. Bernardi

Chem. Eur. J. 2015, 21, 17578 –17582

https://doi.org/10.1002/chem.201502655

Catalytic highly enantioselective transfer hydrogenation of b-trifluoromethyl nitroalkenes. An easy and general entry to optically active b-trifluoromethyl amines

Catalytic highly enantioselective transfer hydrogenation of b-trifluoromethyl nitroalkenes. An easy and general entry to optically active b-trifluoromethyl amines

 

E. Martinelli, A. C. Vicini, M. Mancinelli, A. Mazzanti, P. Zani, L. Bernardi, M. Fochi

Chem. Commun., 2015, 51, 658--660

https://doi.org/10.1039/C4CC07801B

Chiral nanostructuring of multivalent macrocycles in solution and on surfaces

Chiral nanostructuring of multivalent macrocycles in solution and on surfaces

 

M. Caricato, A. Delforge, D. Bonifazi, D. Dondi, A. Mazzanti, D. Pasini

Org. Biomol. Chem., 2015, 13, 3593–3601

https://doi.org/10.1039/C4OB02643H

Enantioselective Preparation, Conformational Analysis and Absolute Configuration of Highly Substituted Aziridines

Enantioselective Preparation, Conformational Analysis and Absolute Configuration of Highly Substituted Aziridines

 

G. Bencivenni, P. Righi, L. Lunazzi, S. Ranieri, M. Mancinelli, A. Mazzanti

Chirality 201527, 875–887

 https://doi.org/10.1002/chir.22522

Long-Range Bonding/Nonbonding Interactions: A Donor–Acceptor Resonance Studied by Dynamic NMR

Long-Range Bonding/Nonbonding Interactions: A Donor–Acceptor Resonance Studied by Dynamic NMR

 

R. Ruzziconi, S. Lepri, F. Buonerba, M. Schlosser, M. Mancinelli, S. Ranieri, L. Prati, A. Mazzanti

Org. Lett. 2015, 17, 2740−2743


https://doi.org/10.1021/acs.orglett.5b01152

 

Me2Zn-Mediated Catalytic Enantio- and Diastereoselective Addition of TosMIC to Ketones

Me2Zn-Mediated Catalytic Enantio- and Diastereoselective Addition of TosMIC to Ketones

 

A. R. Keeri, A. Gualandi, A. Mazzanti, J. Lewinski, P. G. Cozzi

Chem. Eur. J. 2015, 21,18949 –18952

 https://doi.org/10.1002/chem.201504362

Organocatalytic Atroposelective Formal Diels−Alder Desymmetrization of N‑Arylmaleimides

Organocatalytic Atroposelective Formal Diels−Alder Desymmetrization of N‑Arylmaleimides

 

F. Eudier, P. Righi, A. Mazzanti, A. Ciogli, G. Bencivenni

Org. Lett. 2015, 17, 1728−1731

https://doi.org/10.1021/acs.orglett.5b00509

Structure and conformational dynamics of an aromatic sulfonamide: NMR, X-Ray and computational studies

Structure and conformational dynamics of an aromatic sulfonamide: NMR, X-Ray and computational studies

S. Menichetti, C. Biagioli, C. Viglianisi, L. Tofani, L. Lunazzi, M. Mancinelli, A. Mazzanti

Arkivic 2015, iv, 66-79

http://dx.doi.org/10.3998/ark.5550190.p008.974

Synthesis and antimicrobial activity of novel structural hybrids ofbenzofuroxan and benzothiazole derivatives

Synthesis and antimicrobial activity of novel structural hybrids ofbenzofuroxan and benzothiazole derivatives

 

E. Chugunova, C. Boga, I. Sazykin, S. Cino, G. Micheletti, A. Mazzanti, M. Sazykina, A. Burilov, L. Khmelevtsova, N. Kostina

European Journal of Medicinal Chemistry 2015, 93, 349-359

https://doi.org/10.1016/j.ejmech.2015.02.023

Vinylogous Reactivity of Oxindoles Bearing Nonsymmetric 3‑Alkylidene Groups

Vinylogous Reactivity of Oxindoles Bearing Nonsymmetric 3‑Alkylidene Groups

 

N. Di Iorio, P. Righi, S. Ranieri, A. Mazzanti, R. G. Margutta, G. Bencivenni

J. Org. Chem. 2015, 80, 7158−7171

https://doi.org/10.1021/acs.joc.5b01022

Alginic acid aerogel: a heterogeneous Brønsted acid promoter for the direct Mannich reaction.

Alginic acid aerogel: a heterogeneous Brønsted acid promoter for the direct Mannich reaction.

 

Asja Pettignano, Luca Bernardi, Mariafrancesca Fochi, Lorenzo Geraci, Mike Robitzer, Nathalie Tanchoux and Françoise Quignard

New J. Chem., 2015, 39, 4222-4226

https://pubs.rsc.org/en/content/articlelanding/2015/NJ/c5nj00349k#!divAbstract

The Emergence of Quinone Methides in Asymmetric Organocatalysis

The Emergence of Quinone Methides in Asymmetric Organocatalysis

Mariafrancesca Fochi, Lorenzo Caruana and Luca Bernardi

Molecules 2015, 20, 11733-11764

OPEN ACCESS

https://www.mdpi.com/1420-3049/20/7/11733

 

Organocatalytic Asymmetric Conjugate Additions to Cyclopent-1-enecarbaldehyde: A Critical Assessment of Organocatalytic Approaches towards the Telaprevir Bicyclic Core

Organocatalytic Asymmetric Conjugate Additions to Cyclopent-1-enecarbaldehyde: A Critical Assessment of Organocatalytic Approaches towards the Telaprevir Bicyclic Core

 

Luca Bernardi, Mariafrancesca Fochi, Riccardo Carbone, Ada Martinelli, Martin E. Fox, Christopher J. Cobley, Bhaskar Kandagatla, Srinivas Oruganti, Vilas H. Dahanukar and Armando Carlone

Chem. Eur. J. 2015, 21, 19208–19222

 https://doi.org/10.1002/chem.201503352