C. Faggi

发表

The Anancomeric Character of the Pharmacophore 1,3,4-Thiadiazoline Framework in Chiral Spiro-Cyclohexyl Derivatives: Effects on Stereochemistry and Spiro-Junction Lability. Thermodynamic Aspects.

S. Carradori, L. Mannina, D. Secci, 2015, The Journal of organic chemistry.

Glucocerebrosidase (GCase) activity modulation by 2-alkyl trihydroxypiperidines: Inhibition and pharmacological chaperoning.

P. Paoli, S. Giachetti, A. Morrone, 2020, Bioorganic chemistry.

Two-step one-pot synthesis of dihydropyrazinones as Xaa-Ser dipeptide isosteres through morpholine acetal rearrangement.

A. Trabocchi, E. Lenci, G. Menchi, 2015, Organic & biomolecular chemistry.

Isolation of ugi four-component condensation primary adducts: a straightforward route to isocoumarins.

M. García-Valverde, G. Menchi, S. Marcaccini, 2010, Organic letters.

Maleimide cycloadditions by sulfinyldienes: is the sulfur configuration the only controller of the diastereofacial selectivity?

A. Marrocchi, C. Faggi, M. Aversa, 2005 .

Thiacyclophane cages and related bi- and tripodal molecules via transient polysulfenic acids.

T. Papalia, C. Faggi, M. Aversa, 2007, The Journal of organic chemistry.

Mono‐ and Trinuclear Tripodal Platinum(II) Chelated Complexes Containing a Pyridine/Sulfoxide Based Anchoring Framework

L. Monsù Scolaro, M. Plutino, L. M. Scolaro, 2013 .

Drug design, synthesis, in vitro and in silico evaluation of selective monoaminoxidase B inhibitors based on 3-acetyl-2-dichlorophenyl-5-aryl-2,3-dihydro-1,3,4-oxadiazole chemical scaffold.

S. Alcaro, R. Cirilli, M. Yáñez, 2016, European journal of medicinal chemistry.

Allyl Cyanate/Isocyanate Rearrangement in Glycals: Stereoselective Synthesis of 1-Amino and Diamino Sugar Derivatives

C. Matassini, F. Cardona, C. Faggi, 2020, Organic letters.

Chiral HPLC separation and absolute configuration of novel S-DABO derivatives.

A. Mai, M. Camalli, D. Rotili, 2009, Chirality.

(3S,4S)-1-Benzyl-4-(N-octylcarbamoyloxy)pyrrolidin-3-yl N-octylcarbamate: a low-temperature redetermination

S. Cicchi, G. Ghini, C. Faggi, 2007 .

An enantiopure azasteroidal derivative bearing an isoborneol sulfinyl residue

C. Faggi, M. Aversa, P. Bonaccorsi, 2007 .

Synthesis, HPLC enantioresolution, and X-ray analysis of a new series of C5-methyl pyridazines as N-formyl peptide receptor (FPR) agonists.

G. Bartolucci, C. Vergelli, M. Giovannoni, 2013, Chirality.

Design, Synthesis, and Biological Evaluation of New 1-(Aryl-1 H-pyrrolyl)(phenyl)methyl-1 H-imidazole Derivatives as Antiprotozoal Agents.

P. Mäser, V. Summa, R. Di Santo, 2019, Journal of medicinal chemistry.

A chromatographic study on the exceptional chiral recognition of 2-(benzylsulfinyl)benzamide by an immobilized-type chiral stationary phase based on cellulose tris(3,5-dichlorophenylcarbamate).

S. Carradori, D. Secci, R. Cirilli, 2018, Journal of chromatography. A.

Approaches towards the synthesis of 7-halo-1,2-dihydroxyindolizidines (7-halolentiginosines) thwarting Grob fragmentation processes

S. Grelli, A. Brandi, F. M. Cordero, 2015 .

Influence of the nature of alkyl substituents on the high-performance liquid chromatography enantioseparation and retention of new atropisomeric 1,1'-bibenzimidazole derivatives on amylose tris(3,5-dimethylphenylcarbamate) chiral stationary phase.

R. Cirilli, Sergio Menta, C. Faggi, 2014, Journal of chromatography. A.

Regioselective electrophilic access to naphtho[1,2-b:8,7-b']- and -[1,2-b:5,6-b']dithiophenes.

S. Menichetti, P. Procacci, C. Viglianisi, 2013, The Journal of organic chemistry.

A chromatographic study on the exceptional enantioselectivity of cellulose tris(4-methylbenzoate) towards C5-chiral 4,5-dihydro-(1H)-pyrazole derivatives.

S. Alcaro, R. Cirilli, R. Ferretti, 2011, Journal of chromatography. A.

Semipreparative HPLC enantioseparation, chiroptical properties, and absolute configuration of two novel cyclooxygenase-2 inhibitors.

S. Fiore, D. Secci, R. Cirilli, 2010, Chirality.

4-Nitroisoxazoles as nitroalkene heterodienes: diastereoselective synthesis of spiro tricyclic nitroso acetals by thermal reactions with ethyl vinyl ether

A. Danesi, D. Giomi, C. Faggi, 2001 .

Enantioselective Synthesis of (7R,8R,8aR)‐ and (7S,8S,8aS)‐7‐Hydroxy‐8‐indolizidinemethanol by 1,3‐Dipolar Cycloaddition of 1‐Pyrroline N‐Oxide to Chiral Pentenoates

A. Brandi, F. M. Cordero, C. Faggi, 2000 .

Separation and identification of volatile and non‐volatile compounds of wine by sorbent extraction and capillary gas chromatography

F. Capozzi, C. Faggi, N. Gelsomini, 1990 .

Yttrium‐Amidopyridinate Complexes: Synthesis and Characterization of Yttrium‐Alkyl and Yttrium‐Hydrido Derivatives

A. Rossin, G. Giambastiani, C. Bianchini, 2010 .

Preparation of N‐Glycosylhydroxylamines and Their Oxidation to Nitrones for the Enantioselective Synthesis of Isoxazolidines

S. Cicchi, M. Marradi, C. Faggi, 2003 .

Enantioselectivity in cardioprotection induced by (S)- (-)-2,2-dimethyl-N-(4'-acetamido-benzyl)-4-spiromorpholone-chromane.

S. Rapposelli, V. Calderone, R. Cirilli, 2009, Journal of medicinal chemistry.

Transformation of .alpha.- and .beta.-ionones into .alpha.- and .beta.-damascone and .beta.-damascenone using allylsilane chemistry

M. Taddei, C. Faggi, N. Gelsomini, 1990 .

Synthesis of enantiopure indolizinones by cascade ring enlargements of 4'-chlorospiro[cyclopropane-1,5'-isoxazolidines].

A. de Meijere, S. Cicchi, A. Brandi, 2006, The Journal of organic chemistry.

1,2,5-Oxadiazole (Furazan) Derivatives from Benzoylnitromethane and Dipolarophiles in the Presence of DABCO: Structure and Intermediates

F. Machetti, C. Faggi, F. Sarlo, 2006 .

New enantiopure C2 symmetric bis(2-oxazolinyl)cage (Cage-Box) ligands from 4,5-dicyanopyridazine

D. Giomi, C. Faggi, M. Cecchi, 2005 .

Synthesis of 1,2-dihydroxyindolizidines from 1-(2-pyridyl)-2-propen-1-ol.

A. Brandi, D. Giomi, C. Faggi, 2011, The Journal of organic chemistry.

Cycloaddition Reactions of C,N-Diphenylnitrone to Methylene-γ-butyrolactones

M. Cacciarini, F. M. Cordero, C. Faggi, 2000 .

Polyhydroxyamino‐Piperidine‐Type Iminosugars and Pipecolic Acid Analogues from a D‐Mannose‐Derived Aldehyde

C. Matassini, F. Cardona, I. Robina, 2014 .

Gold(I)-Catalyzed Cycloisomerization/Hetero-Diels-Alder Reaction/Ring Opening Cascade to Functionalized Cyclopentadienes.

E. Gómez-Bengoa, C. Faggi, D. Scarpi, 2022, The Journal of organic chemistry.

Easy one-step general synthesis of acylsilanes

A. Degl'innocenti, A. Capperucci, C. Faggi, 1988 .

Configuration-guided reactions: the case of highly decorated spiro[cyclopropane-1,2′(3′H)-pyrrolo[1,2-b]isoxazole] derivatives en route to polyhydroxyindolizidines

A. Brandi, F. M. Cordero, C. Faggi, 2016 .

Transformations of α- and β-Ionones into α- and β-Damascone and β-Damascenone Using Allylsilane Chemistry.

M. Taddei, C. Faggi, N. Gelsomini, 1990 .

o-Thioquinones on [2.2]paracyclophanes: an example of totally stereocontrolled hetero Diels–Alder reactions

S. Menichetti, G. Lamanna, A. Marrocchi, 2006 .

Thia-Bridged Triarylamine Hetero[4]Helicenes: Regioselective Synthesis and Functionalization

S. Menichetti, M. Maggini, C. Viglianisi, 2018, European Journal of Organic Chemistry.

Preparation and cycloaddition reactions of enantiopure 2-(N-acylamino)-1,3-dienes for the synthesis of octahydroquinoline derivatives.

A. Guarna, C. Faggi, E. Occhiato, 2003, The Journal of organic chemistry.

Click Reaction of Selenols with Isocyanates: Rapid Access to Selenocarbamates as Peroxide‐Switchable Reservoir of Thiol‐Peroxidase‐Like Catalysts

A. Capperucci, A. Petrucci, C. Faggi, 2021, Advanced Synthesis & Catalysis.

Double addition of grignard reagents to N-glycosyl nitrones: a new tool for the construction of enantiopure azaheterocycles.

S. Cicchi, M. Marradi, C. Faggi, 2005, Organic letters.

Allylsilanes derived from α- and β-ionone. Synthesis and unusual reactivity with electrophiles

M. Taddei, C. Faggi, N. Gelsomini, 1989 .

Application of an immobilised amylose-based chiral stationary phase to the development of new monoamine oxidase B inhibitors.

R. Cirilli, E. Maccioni, C. Faggi, 2010, Talanta.

A general access to acylstannanes

A. Degl'innocenti, A. Capperucci, G. Reginato, 1989 .

Accessing 2-substituted piperidine iminosugars by organometallic addition/intramolecular reductive amination: aldehyde vs. nitrone route.

C. Matassini, F. Cardona, G. Fibbi, 2017, Organic & biomolecular chemistry.

The reaction of Ru(CO)2(MeCO2)2(PR3)2 or Ru2(CO)4(MeCO2)2(PR3)2 [RBu, Ph] with H2 in the presence of Na2CO3: a stoichiometric carbon dioxide activation

P. Frediani, A. Salvini, C. Faggi, 1998 .

Efficient Thia-bridged triarylamine heterohelicenes: synthesis, resolution, and absolute configuration determination.

S. Menichetti, P. Stephens, F. Devlin, 2008, Chemistry.

Behaviour of triphenylphosphine-substituted ruthenium carbonyl carboxylates with hydrogen

P. Frediani, A. Salvini, M. Nardelli, 1997 .

Quasienantiomeric levoglucosenone and isolevoglucosenone allow the parallel kinetic resolution of a racemic nitrone.

D. Lalli, F. Cardona, A. Brandi, 2008, Journal of Organic Chemistry.

Mass spectral studies of some 1,2,4‐oxa‐(thia)diazol‐5(4H)‐ones(thiones)

C. Faggi, Y. Dürüst, 1997 .

Mass Spectral Studies of Some 1,2,4‐Oxa(thia)diazol‐5(4H)‐ones(thiones).

C. Faggi, Y. Dueruest, 1998 .

Enantiopure arenesulfenic acids as intermediates in stereoselective synthesis

S. Menichetti, G. Lamanna, C. Faggi, 2005 .

Copper-Catalyzed A3 -Coupling for the Diversity-Oriented Synthesis of Proline-Derived Alkynyl-Substituted Peptidomimetic Scaffolds

A. Trabocchi, E. Lenci, G. Menchi, 2019, European Journal of Organic Chemistry.

Novel l-TartaricAcid Derived Pyrrolidinium Cations for the Synthesis of Chiral IonicLiquids

F. Cardona, C. Faggi, A. Goti, 2009 .