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2018

Stereodynamic Analysis of New Atropisomeric 4,7-Di(naphthalen-1-yl)-5,6-dinitro-1 H -indoles

Stereodynamic Analysis of New Atropisomeric 4,7-Di(naphthalen-1-yl)-5,6-dinitro-1 H -indoles

A. Pagano, E. Marotta, A. Mazzanti, G. Petrillo, C. Tavani, M. Mancinelli

Synlett 201829, 2161-2166

https://www.thieme-connect.de/products/ejournals/abstract/10.1055/s-0037-1609908

Enantioselective Synthesis of Trifluoromethyl α, β-Unsaturated δ-Lactones via Vinylogous Aldol-Lactonization Cascade

Enantioselective Synthesis of Trifluoromethyl α, β-Unsaturated δ-Lactones via Vinylogous Aldol-Lactonization Cascade

S. Crotti, N. Di Iorio, A. Mazzanti, P. Righi, G. Bencivenni

J. Org. Chem. 2018, 83, 12440-12448

https://doi.org/10.1021/acs.joc.8b01672

Synergistic Catalysis: Highly Enantioselective Acetyl Aza‐arene Addition to Enals

Synergistic Catalysis: Highly Enantioselective Acetyl Aza‐arene Addition to Enals

M. Meazza, G. Sitinova, C. Poderi, M. Mancinelli, K. Zhang, A. Mazzanti

Chemistry–A European Journal , 2018, 24, 13306-13310

https://doi.org/10.1002/chem.201802303

Quinone‐Fused Pyrazoles through 1, 3‐Dipolar Cycloadditions: Synthesis of Tricyclic Scaffolds and in vitro Cytotoxic Activity Evaluation on Glioblastoma Cancer Cells

Quinone‐Fused Pyrazoles through 1, 3‐Dipolar Cycloadditions: Synthesis of Tricyclic Scaffolds and in vitro Cytotoxic Activity Evaluation on Glioblastoma Cancer Cells

G. Bertuzzi, S. Crotti, P. Calandro, B. F. Bonini, I. Monaco, E. Locatelli, M. Fochi, P. Zani, E. Strocchi, A. Mazzanti, M. Chiariello, M. Comes Franchini

ChemMedChem 2018, 13, 1744-1750

https://doi.org/10.1002/cmdc.201800251

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, B. Formánek, A. Mazzanti, J. Roithová, J. Veselý, R. Rios

Chemical Science 2018, 9, 6368-6373

https://doi.org/10.1039/C8SC00913A

Click to view Correction:

https://doi.org/10.1039/C9SC90160D

Catalytic Enantioselective Povarov Reactions of Ferrocenecarbaldehyde‐Derived Imines–Brønsted Acid Catalysis at Parts‐Per‐Million Level Loading

Catalytic Enantioselective Povarov Reactions of Ferrocenecarbaldehyde‐Derived Imines–Brønsted Acid Catalysis at Parts‐Per‐Million Level Loading

Dragana Stevanović, Giulio Bertuzzi, Andrea Mazzanti, Mariafrancesca Fochi and Luca Bernardi

Advanced Synthesis & Catalysis 2018, 360, 893-900

https://doi.org/10.1002/adsc.201701484

Enantioselective Dearomatization of Alkylpyridiniums by N-Heterocyclic Carbene-Catalyzed Nucleophilic Acylation

Enantioselective Dearomatization of Alkylpyridiniums by N-Heterocyclic Carbene-Catalyzed Nucleophilic Acylation

G. Di Carmine, D. Ragno, O. Bortolini, P.P. Giovannini, A. Mazzanti, A. Massi, M. Fogagnolo

J. Org. Chem. 2018, 83, 2050-2057

https://doi.org/10.1021/acs.joc.7b02996

Asymmetric vinylogous aldol addition of alkylidene oxindoles on trifluoromethyl-α, β-unsaturated ketones

Asymmetric vinylogous aldol addition of alkylidene oxindoles on trifluoromethyl-α, β-unsaturated ketones

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

RSC Advances 2018, 8, 33451-33458

https://doi.org/10.1039/C8RA06615A

Catalytic enantioselective one-pot approach to cis-and trans-2, 3-diaryl substituted 1, 5-benzothiazepines

Catalytic enantioselective one-pot approach to cis-and trans-2, 3-diaryl substituted 1, 5-benzothiazepines

S. Meninno, I. Quaratesi, C. Volpe, A. Mazzanti, A. Lattanzi

Organic & Biomolecular Chemistry 2018, 16, 6923-6934

https://doi.org/10.1039/C8OB01988F

An organocatalytic enantioselective direct α-heteroarylation of aldehydes with isoquinoline N-oxides

 An organocatalytic enantioselective direct α-heteroarylation of aldehydes with isoquinoline N-oxides

Giulio Bertuzzi, Daniel Pecorari, Luca Bernardi, and Mariafrancesca Fochi

Chem. Commun., 2018, 54, 3977–3980

https://pubs.rsc.org/en/content/articlelanding/2018/cc/c8cc01735b#!divAbstract

gamma-Regioselective Functionalization of 3-Alkenylindoles via 1,6-Addition to Extended Alkylideneindolenine Intermediates

gamma-Regioselective Functionalization of 3-Alkenylindoles via 1,6-Addition to Extended Alkylideneindolenine Intermediates

Giulio Bertuzzi, Lucia Lenti, Denisa Giorgiana Bisag, Mariafrancesca Fochi, Marino Petrini, and Luca Bernardi

Adv. Synth. Catal. 2018, 360, 1296 – 1302

https://doi.org/10.1002/adsc.201701558

Nucleophilic Dearomatization of Activated Pyridines

Nucleophilic Dearomatization of Activated Pyridines

Giulio Bertuzzi, Luca Bernardi, and Mariafrancesca Fochi

Catalysts 2018, 8, 632

OPEN ACCESS

https://www.mdpi.com/2073-4344/8/12/632