M. Marzi

发表

N-Hydroxy-(4-oxime)-cinnamide: a versatile scaffold for the synthesis of novel histone deacetylase [correction of deacetilase] (HDAC) inhibitors.

G. Giannini, C. Pisano, L. Vesci, 2009, Bioorganic & medicinal chemistry letters.

Bis-indols: a novel class of molecules enhancing the cytodifferentiating properties of retinoids in myeloid leukemia cells.

C. Pisano, F. F. Ferrara, L. Vesci, 2002, Blood.

Exploring bis-(indolyl)methane moiety as an alternative and innovative CAP group in the design of histone deacetylase (HDAC) inhibitors.

G. Giannini, C. Pisano, L. Vesci, 2009, Bioorganic & medicinal chemistry letters.

Towards the development of 5-HT₇ ligands combining serotonin-like and arylpiperazine moieties.

M. Mor, G. Tarzia, W. Cabri, 2014, European journal of medicinal chemistry.

Omega-alkoxy analogues of SAHA (vorinostat) as inhibitors of HDAC: a study of chain-length and stereochemical dependence.

G. Giannini, S. Hanessian, C. Pisano, 2007, Bioorganic & medicinal chemistry letters.

Design, synthesis, and structure-activity relationship of N-arylnaphthylamine derivatives as amyloid aggregation inhibitors.

R. Di Santo, R. Costi, S. Caccia, 2012, Journal of medicinal chemistry.

Exploring alternative Zn-binding groups in the design of HDAC inhibitors: squaric acid, N-hydroxyurea, and oxazoline analogues of SAHA.

G. Giannini, S. Hanessian, L. Auzzas, 2006, Bioorganic & medicinal chemistry letters.

Reversible carnitine palmitoyltransferase inhibitors with broad chemical diversity as potential antidiabetic agents.

A. Arduini, R. Conti, M. Mabilia, 2001, Journal of medicinal chemistry.

Synthetic studies in the intramolecular carbocyclization of N-acyloxyiminium ions. Stereoelectronic and steric implications of nucleophilic alkene, alkyne, and allene tethers.

J. D. Del Valle, S. Hanessian, M. Tremblay, 2005, The Journal of organic chemistry.

Studies related to cephalosporins. Part 2 . Displacement reactions on 3‐bromomethylcephems with salts of carboxylic acids

F. Angelis, M. Botta, R. Nicoletti, 1985 .

Synthesis of enantiomerically pure (2R, 5R) disubstituted pyrrolidines from D-mannitol

M. Marzi, D. Misiti, P. Minetti, 1992 .

Efficient enantioselective synthesis of (R)-(-)-carnitine from glycerol.

F. De Angelis, M. Marzi, P. Minetti, 2000, The Journal of organic chemistry.

E-ring-modified 7-oxyiminomethyl camptothecins: Synthesis and preliminary in vitro and in vivo biological evaluation.

G. Giannini, F. Zunino, C. Pisano, 2008, Bioorganic & medicinal chemistry letters.

Asymmetric synthesis of trans-(2R,5R)-bis(benzyloxymethyl)pyrrolidine

M. Marzi, D. Misiti, 1989 .

Synthesis and biological activity of fluorinated combretastatin analogues.

G. Giannini, C. Pisano, W. Cabri, 2008, Journal of medicinal chemistry.

Corrigendum to “N-Hydroxy-(4-oxime)-cinnamide: A versatile scaffold for the synthesis of novel histone deacetilase (HDAC) inhibitors” [Bioorg. Med. Chem. Lett. 19 (2009) 2346]

G. Giannini, C. Pisano, L. Vesci, 2009 .