M. P. Paradisi

发表

β-Peptido sulfonamides: for-Met-Leu-Phe-OMe analogues containing taurine and chiral β-amino-ethanesulfonic acid residues

M. Nalli, A. Sansone, S. Spisani, 2004 .

Biscarbamate analogues of the chemotactic tripeptide fMLF-OMe.

M. Nalli, S. Spisani, G. Lucente, 2000, Farmaco.

Chemotactic Peptide Analogues Centrally Constrained Chemotactic N‐Formyltripeptides: Synthesis, Conformation, and Activity of Two New Analogues

M. Paci, S. Spisani, G. Lucente, 1996 .

Chemotactic Peptide Analogues The Role of (Z)‐2,3‐Didehydrophenylalanine and Phenylalanine C‐Terminal Residues in Determining the Chemotactic Activity of Formylpeptides

S. Spisani, M. P. Paradisi, I. Torrini, 1996, Archiv der Pharmazie.

Chemotactic Peptide Analogues. Synthesis and Chemotactic Activity of N‐Formyl‐Met‐Leu‐Phe Analogues Containing (S)‐Phenylalaninol Derivatives

S. Spisani, M. P. Paradisi, I. Torrini, 1995, Archiv der Pharmazie.

Modified chemotactic peptides: Synthesis, conformation, and biological activity of for‐Thp‐Leu‐ΔzPhe‐OMe

G. Cerichelli, G. Pochetti, S. Traniello, 1994 .

Two new formylated peptides able to activate chemotaxis and respiratory burst selectively as tools for studying human neutrophil responses.

M. Pareschi, M. E. Ferretti, C. Biondi, 1994, Cellular signalling.

Modified chemotactic peptides: synthesis, crystal conformation, and activity of For‐Hse(Me)‐Leu‐Phe‐OMe

G. Pochetti, S. Traniello, S. Spisani, 1994, Biopolymers.

Cyclic Analogs of Chemotactic Formylpeptides, I.: Synthesis and Biological Activity of For‐Cys‐Leu‐Phe‐Cys‐OMe

S. Traniello, S. Spisani, G. Lucente, 1993, Archiv der Pharmazie.

Synthesis and Chemotactic Activity of the fMLP Analog HCO‐Hmb‐Leu‐Phe‐OMe

S. Traniello, S. Spisani, G. Lucente, 1993, Archiv der Pharmazie.

Topographically constrained aromatic α-aza-amino acids. Part 2. New azaTic-containing peptides: Synthesis, conformation, and intramolecular NH…N interaction

F. Mazza, G. Lucente, G. Mastropietro, 1999 .

α-Peptide/β-sulfonamidopeptide hybrids: Analogs of the chemotactic agent for-Met-Leu-Phe-OMe

A. Masi, A. Sansone, S. Spisani, 2006 .

Chemotactic peptides: fMLF-OMe analogues incorporating proline-methionine chimeras as N-terminal residue.

A. Mollica, K. Varani, S. Spisani, 2006, Bioorganic & medicinal chemistry.

Synthesis of peptides containing 1,2,3,4-tetrahydroquinoline-2-carboxylic acid. Part 1. Absolute configurations of 1,2,3,4-tetrahydroquinoline-2-carboxylic acids and 2-substituted 1,2,3,4-tetrahydroquinolines.

M. P. Paradisi, A. Romeo, 1977, Journal of the Chemical Society. Perkin transactions 1.

The reactivity of 2,3-diaminopyridine toward alkyl chloroformates and dicarbonates

M. P. Paradisi, I. Torrini, G. P. Zecchini, 1985 .

Synthesis of some 2,3-Dihydro-11bH-thiazolo[3,2-d][1,4]benzoxazepin-5-(6H)one derivatives. A new heterocyclic ring system

M. P. Paradisi, I. Torrini, A. Romeo, 1981 .

A convenient route to pyrrolidine-2-phosphonic acid dipeptides

G. Lucente, M. P. Paradisi, I. Torrini, 2009 .

Synthesis of quino[2,3-b][1,5]benzoxazepines: a novel tetracyclic ring system

M. P. Paradisi, I. Torrini, G. P. Zecchini, 1987 .

Synthesis of peptides containing 1,2,3,4‐tetrahydroquinoline‐2‐carboxylic acid. Part 3. Cyclization of dipeptides and amides with acetic anhydride

M. P. Paradisi, G. P. Zecchini, 1979 .

Synthesis of peptides containing 1,2,3,4-tetrahydroquinoline-2-carboxylic acid. Part 2. Crystal and molecular structure of a 1H,3H,5H-oxazolo[3,4-a]quinolin-3-one derivative obtained from a linear tripeptide

W. Fedeli, F. Mazza, G. Lucente, 1979 .

Dehydration of β-Hydroxy-α-amino Acid Derivatives With Phenyltriflimide

M. P. Paradisi, I. Torrini, G. P. Zecchini, 1989 .

Proline-glutamate chimeras in isopeptides. Synthesis and biological evaluation of conformationally restricted glutathione analogues.

A. Mollica, A. Caccuri, A. Di Stefano, 2003, Bioorganic & medicinal chemistry.

Synthesis, stereochemistry and conformational properties of diastereomeric cyclic dipeptides containing tetrahydro-1,4-thiazine-3,5-dicarboxylic acid

G. Lucente, M. P. Paradisi, I. Torrini, 1990 .

Applications of 1-alkoxycarbonyl- and 1-acyl-v-triazolo[4,5-b]pyridines as acylating reagents

M. P. Paradisi, I. Torrini, G. P. Zecchini, 1986 .

A new route to N2- and N3-substituted-2,3-diaminopyridines. Synthesis of 1- and 3-alkoxycarbonyl-v-triazolo[4,5-b]pyridines

M. P. Paradisi, I. Torrini, G. P. Zecchini, 1985 .

Synthesis and properties of chemotactic peptide analogs. I. Crystal structure and molecular conformation of HCO-Met-leu-Ain-OMe.

G. Pochetti, F. Mazza, G. Lucente, 2009, International journal of peptide and protein research.

Hydrogenolyses of 3-hydroxycholest-4-enes by mixed hydrides.

M. P. Paradisi, A. Romeo, 1972, Journal of the Chemical Society. Perkin transactions 1.

Inhibition of adamalysin II and MMPs by phosphonate analogues of snake venom peptides.

G. Pochetti, B. Gorini, F. Mazza, 1999, Bioorganic & medicinal chemistry.

Retrosulfonamido peptide analogues. Synthesis and crystal conformation of Boc-Pro-Leu-Ψ(NH-SO2)-Gly-NH2

G. Pochetti, F. Mazza, G. Lucente, 1991 .

Conformational properties of β-residue-containing oligopeptides in apolar solvent

A. Mollica, M. Aschi, F. Mazza, 2006 .

Chemotactic tripeptides incorporating at position 2 α-aminoacid residues with unsaturated side chains

D. Torino, A. Sansone, S. Spisani, 2008, Amino Acids.

Peptides containing the sulfonamide junction: Synthesis, structure, and conformation of Z-Tau-Pro-Phe-NHiPr

M. Paci, G. Luisi, G. Pochetti, 1997 .

Synthesis and properties of chemotactic peptide analogs

G. Pochetti, A. Giuliani, F. Mazza, 2009 .

Reactions of steroid allylic systems: solvolyses of cholest-4-en-3β- and 3α-yl trifluoroacetates

G. Ortar, E. Morera, M. P. Paradisi, 1978 .

Reduction of steroidal dicarbonyl compounds with poly(n-isopropyliminoalane)

M. P. Paradisi, G. P. Zecchini, 1981 .

Selective reduction of 3-keto group in steroidal ketoaldehydes

M. P. Paradisi, G. P. Zecchini, 1982 .

Selective acylations of aminophenols and hydroxyalkylphenols with 1-acetyl-v-triazolo[4,5-b]pyridine

M. P. Paradisi, I. Torrini, G. P. Zecchini, 1986 .

Oxidation of Sulfides to Sulfoxides by 1-Acetyl-v-Triazolo/4,5-b_/Pyridine/Hydrogen Peroxide System

M. P. Paradisi, I. Torrini, G. P. Zecchini, 1987 .

γ-Turn conformation induced by α,α-disubstituted amino acids with a cyclic six-membered side chain

G. Pochetti, F. Mazza, G. Lucente, 1995 .

Synthesis, conformation, and biological activity of two fMLP‐OMe analogues containing the new 2‐[2′‐(methylthio) ethyl] methionine residue

G. Pochetti, S. Traniello, S. Spisani, 1997, Biopolymers.

In situ selective protection of aldehydes via aldimines

M. P. Paradisi, I. Torrini, G. P. Zecchini, 1983 .

For‐Met‐Lys‐Phe‐ For‐Met‐Lys‐Phe‐: A new cyclic analogue of the chemotactic formylpeptides

G. Pochetti, S. Traniello, S. Spisani, 1995, Biopolymers.

Synthesis, conformation, and activity of HCO‐Met‐ΔZ Leu‐Phe‐Ome, an active analogue of chemotactic N‐formyltripeptides

G. Veglia, M. Paci, G. Pochetti, 1993, Biopolymers.

In situ selective protection of aldehydes via aldimines : Simple conversions of ketoaldehydes to methylene aldehydes and to methylhydroxy aldehydes

M. P. Paradisi, I. Torrini, G. P. Zecchini, 1984 .

Modified chemotactic peptides: synthesis, conformation, and activity of HCO-Thp-Ac6c-Phe-OMe.

G. Pochetti, S. Traniello, S. Spisani, 1998, Biopolymers.

Synthesis, conformation and biological activity of centrally modified pseudopeptidic analogues of For-Met-Leu-Phe-OMe

A. Masi, A. Sansone, S. Spisani, 2007, Amino Acids.

2 Å X‐ray structure of adamalysin II complexed with a peptide phosphonate inhibitor adopting a retro‐binding mode

G. Pochetti, B. Gorini, F. Gomis-ruth, 1997 .