G. Porzi

发表

Electrostatic interactions effect in the aminolysis of some β‐lactams in the presence of poly(ethyleneimine):structure‐reactivity

Monica Sandri, Samuele Rinaldi, A. Arcelli, 2008 .

Cyclization of .alpha.,.omega. aliphatic diamines and conversion of primary amines to symmetrical tertiary amines by a homogeneous ruthenium catalyst

G. Porzi, C. Concilio, 1981 .

Selective conversion of primary amines into N,N-dimethylalkyl- or N,N-dialkylmethyl-amines with methanol and RuCl2(Ph3P)3

A. Arcelli, G. Porzi, Bui-The-Khai, 1982 .

Stereoselective synthesis of pseudotripeptides incorporating uncommon bis-α-aminoacid derivatives and X-ray analysis. Part 3

A. Grandi, G. Porzi, P. Sabatino, 2004 .

Acidity effect on the cleavage of ether function intramolecularly assisted by the amide group. Part 5

A. Arcelli, G. Porzi, S. Rinaldi, 2001 .

Mechanistic investigation of an anomalous anchimeric assistance in the acid hydrolysis of the ether linkage. Part 4

A. Arcelli, G. Porzi, S. Rinaldi, 2001 .

Stereoselective synthesis of a new chiral synthon: a cyclic pseudodipeptide containing an aspartic acid derivative and l-valine

A. Grandi, G. Porzi, S. Sandri, 2006 .

Stereocontrolled synthesis of unnatural cyclic dipeptides containing an l-valine unit

A. Grandi, G. Porzi, S. Sandri, 2005 .

Enantioselective synthesis of pseudotripeptides incorporating a γ-methylene derivative of 2,6-diaminopimelic acid: Part 6

G. Porzi, S. Sandri, Daniele Balducci, 2004 .

Stereoselective synthesis of bis(α-amino acid) derivatives isosteric of cysteine. Part 4

G. Porzi, F. Ferioli, F. Piccinelli, 2002 .

A new stereocontrolled synthesis of uncommon tripeptides derived from 2,6-diaminopimelic acid (2,6-DAP)

G. Porzi, F. Paradisi, S. Sandri, 2001 .

(S)-α-methyl,α-amino acids: a new stereocontrolled synthesis

G. Porzi, F. Piccinelli, M. Monari, 2010, Amino Acids.

Acid Hydrolysis of an Ether Bond Assisted by the Neighbouring Amide Group: Effects Induced by Salts and by Structural Changes Part 61-5

A. Arcelli, G. Porzi, S. Rinaldi, 2002 .

Ammonolysis of morpholine-2,5-diones: participation of the primary amide group. Part 2

A. Arcelli, G. Porzi, S. Rinaldi, 2012 .

Regio- and stereocontrolled synthesis of epoxy alcohols and triols from allylic and homoallylic alcohols via iodocarbonates

G. Porzi, A. Bongini, G. Cardillo, 1982 .

A new regio- and stereo-selective functionalization of allylic and homoallylic alcohols

G. Porzi, G. Cardillo, M. Orena, 1981 .

Stereocontrolled Synthesis of Unnatural Tetrapeptides Containing L‐Valine Units. Part 3

G. Porzi, Daniele Balducci, 2011 .

A highly efficient stereocontrolled synthesis of ( S )-2′,6′-dimethyltyrosine [( S )-DMT]

G. Porzi, Daniele Balducci, S. Contaldi, 2009 .

A facile synthesis of symmetrical secondary amines from primary amines promoted by the homogeneous catalyst RuCl2(Ph3P)3

G. Porzi, C. Concilio, Bui-The-Khai, 1981 .

Diastereoselective alkylation of (3S)- and (3R)-3-methylpiperazine-2,5-dione derivatives. A convenient approach to both (S)- and (R)-alanine

G. Porzi, M. Orena, S. Sandri, 1992 .

Enantioselective synthesis of (R)-and (S)-α-aminoacids using (6S)- and (6R)-6-methyl-morpholine-2,5-dione derivatives

G. Porzi, S. Sandri, 1996 .

Novel synthesis of .alpha.-hydroxy ketones and .gamma.- or .delta.-keto esters from cyclic iodo carbonates and iodo lactones

G. Porzi, C. Tomasini, G. Cardillo, 1984 .

Synthesis of Aminoalcohols via Perihydro-1,3-oxazin-2-ones and Absolute Configuration Assignment through MM2 Calculations

G. Porzi, A. Bongini, G. Cardillo, 1988 .

Carbonate Ion on a Polymeric Support: Hydrolysis of Alkyl Halides and Cyclic Iodocarbonates

G. Porzi, G. Cardillo, M. Orena, 1981 .

A simple asymmetric synthesis of (+)- and (−)-2,6-diaminopimelic acids

G. Porzi, S. Rinaldi, F. Paradisi, 2000 .

Stereoselective synthesis of α,α′-diamino-dicarboxylic acids. Part 2☆

G. Porzi, S. Rinaldi, F. Paradisi, 2000 .

Highly stereocontrolled boron-mediated synthesis of β-hydroxy-α-amino acids and dipeptides. Part 2

G. Porzi, F. Paradisi, S. Sandri, 1999 .

A new stereoselective synthesis of sterically constrained uncommon α,α′-dialkylated α-amino acids. Part 2

G. Porzi, S. Sandri, 1998 .

A new approach to 2-phenylthioalcohols in high optical purity

G. Porzi, M. Orena, S. Sandri, 1992 .

Halogen—metal interconversion in 2,7-dibromonaphthalene and 2,7-dibromoanthracene

G. Porzi, C. Concilio, 1977 .

Unusual ammonolysis of a secondary amide assisted by unsubstituted vicinal amide group

A. Arcelli, G. Porzi, S. Sandri, 1996 .

A new synthesis of both the enantiomers of 4-amino-3-hydroxybutanoic acid (gabob) and mm2 calculations for rotamers of the intermediate oxazolidin-2-on

G. Porzi, A. Bongini, G. Cardillo, 1987 .

A regioselective introduction of functional groups to the double bonds of allylic and homoallylic alcohols via the corresponding trichloroacetimidates

G. Porzi, G. Cardillo, M. Orena, 1983 .

The homogeneously catalysed synthesis of N-methyldi-alkylamines from n-methyl and N,N-dimethylalkylamines

A. Arcelli, G. Porzi, But-The-Khai, 1982 .

A new stereoselective approach to -hydroxy-a-aminoacids and dipeptides

G. Porzi, S. Sandri, P. D. Felice, 1999 .

Conformational analysis of hexapseudopeptides mimicking reverse turn structures induced by a modified (S)-proline. A combined spectroscopic and molecular dynamics investigation. Part 4

A. Bottoni, G. Porzi, M. Calvaresi, 2009 .

Stereoselective synthesis and conformational analysis of unnatural tetrapeptides. Part 2

A. Bottoni, G. Porzi, M. Calvaresi, 2007 .

Stereoselective synthesis and conformational analysis of pseudo-heptapeptides: Part 5

A. Bottoni, G. Porzi, M. Calvaresi, 2007 .

Synthesis and conformational preferences of unnatural tetrapeptides containing l-valine units

A. Bottoni, G. Porzi, M. Calvaresi, 2006 .

Synthesis and conformational preferences of cyclic unnatural di- and tripeptides containing an l-valine unit: Part 2 ☆

M. Recanatini, G. Porzi, F. Piccinelli, 2005 .

Stereoselective approach to uncommon tripeptides incorporating a 2,6-diaminopimelic acid framework: X-ray analysis and conformational studies. Part 4

G. Porzi, R. Galeazzi, F. Piccinelli, 2005 .

Enantioselective Synthesis of (R)- and (S)-α-Aminoacids Using ( 6S)- and (6R)-6-Methyl-morpholine-2,5-dione Derivatives.

G. Porzi, S. Sandri, 2010 .

Benzylpenicillin cleavage with polyelectrolytes

A. Arcelli, G. Porzi, M. Sandri, 2005 .

Unusual peptides containing the 2,6-diaminopimelic acid framework: Stereocontrolled synthesis, X-ray analysis, and computational modelling. Part 2

A. Grandi, G. Porzi, M. Garavelli, 2003 .

Degradation and mobility of metolachlor and terbuthylazine in a sandy clay loam soil

G. Porzi, L. Leita, C. Vischetti, 1998 .

Synthesis of new chiral 1,4 -morpholin -2,5 -dione derivatives and evaluation as α-glucosidase inhibitors. Part 3

A. Arcelli, G. Porzi, M. Sandri, 2007 .

Chiral 1,4-morpholin-2,5-dione derivatives as α-glucosidase inhibitors: Part 2

A. Grandi, A. Arcelli, G. Porzi, 2005 .

Chiral 1,4-Morpholine-2,5-diones. Synthesis and Evaluation as Glucosidase Inhibitors

A. Grandi, A. Arcelli, G. Porzi, 2004 .

Effect of neighbouring amide group bulkiness on anchimerically assisted ether bond cleavage: Part 7

A. Arcelli, G. Porzi, S. Rinaldi, 2004 .

An efficient acid hydrolysis of the ether bond assisted by the neighbouring benzamide group. Part 3

A. Arcelli, G. Porzi, S. Rinaldi, 2001 .

Chiral Piperazine‐2,5‐dione Derivatives as Effective α‐Glucosidase Inhibitors. Part 4

A. Arcelli, G. Porzi, M. Sandri, 2010, Chemistry and Biodiversity.

Participation of neighbouring amide group in the competitive acid catalysed hydrolysis of ether linkage and an intramolecular SN2 reactions. 2

A. Arcelli, G. Porzi, M. Papa, 1997 .

Catalytic intramolecular participation of amide group in the acid hydrolysis of methyl ether linkage

A. Arcelli, G. Porzi, S. Sandri, 1995 .

Stereocontrolled synthesis of enantiomerically pure unsaturated analogues of 2,6-DAP. Part 5

G. Porzi, M. Sandri, F. Piccinelli, 2003 .

Synthesis of (3R,6R)- and (3S,6S)-3,6-dialkylpiperazin-2,5-dione derivatives as useful intermediates to both (R) and (S) α-aminoacids

G. Porzi, S. Sandri, 1994 .

Enantioselective synthesis of 2,6-diaminopimelic acid derivatives. Part 3

G. Porzi, F. Paradisi, F. Piccinelli, 2002 .

Synthesis of malyngolide, an antibiotic from the marine blue-green alga Lyngbya majuscula Gomont

G. Porzi, G. Cardillo, M. Orena, 1981 .

NOVEL SYNTHESIS OF α-HYDROXY KETONES AND Γ- OR Δ-KETO ESTERS FROM CYCLIC IODO CARBONATES AND IODO LACTONES

G. Porzi, C. Tomasini, G. Cardillo, 1984 .

Stereoselective synthesis of sterically constrained dipeptides. Part 2

G. Porzi, S. Sandri, P. Verrocchio, 1998 .

Stereoselective synthesis of dipeptides—I

G. Porzi, V. Favero, S. Sandri, 1997 .