M. Orena

发表

Iodocyclofunctionalization of (E)-1-trichloroacetimidoalk-2-enes. Synthesis of (±)-erythro-sphinganine triacetate

A. Bongini, C. Tomasini, G. Cardillo, 1986 .

Synthesis, Structural Insights and Activity of Different Classes of Biomolecules

F. Spinozzi, M. Ortore, F. Tanfani, 2020 .

Magnesium Porphine Supermolecules and Two-Dimensional Nanoaggregates Formed Using the Langmuir-Schaefer Technique.

C. H. Devillers, V. Bykov, O. Koifman, 2018, Langmuir : the ACS journal of surfaces and colloids.

A novel conformationally restricted analogue of 3-methylaspartic acid via stereoselective methylation of chiral pyrrolidin-2-ones

S. Rinaldi, P. Sabatino, R. Galeazzi, 2010 .

Influence of structure on the antioxidant activity of indolinic nitroxide radicals.

J. Antosiewicz, E. Damiani, L. Greci, 1997, Free radical biology & medicine.

Steric constraints against [3,3]-sigmatropic rearrangement of allylic azides. A convenient approach to β-l-4-aminopent-2-enoglyceropyranosides

G. Mobbili, R. Galeazzi, M. Orena, 2001 .

Synthesis of a conformationally restricted analog of pregabalin by stereoselective alkylation of a chiral pyrrolidin-2-one

G. Mobbili, S. Rinaldi, R. Galeazzi, 2003 .

A Bifunctional β‐Isocupreidine Derivative as Catalyst for the Enantioselective Morita–Baylis–Hillman Reaction and a Mechanistic Rationale for Enantioselectivity

S. Rinaldi, G. Martelli, M. Orena, 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 .

Quaternary centres as a tool for modulating foldamer conformation.

A. Mazzanti, S. Rinaldi, R. Galeazzi, 2011, Chemistry.

Imidazolidinone-Tethered α-Hydrazidopeptides - Synthesis and Conformational Investigation

S. Rinaldi, M. Calvaresi, G. Martelli, 2019, European Journal of Organic Chemistry.

Stereocontrolled cyclofunctionalizations of double bonds through heterocyclic intermediates

G. Cardillo, M. Orena, 1990 .

Stereocontrolled cyclofunctionalizations of double bonds through heterocyclic intermediates

G. Cardillo, M. Orena, 1990 .

Role of yeast bioactive compounds in food and fermented beverages

L. Oro, M. Ciani, M. Orena, 2013 .

Stereoselective reductive amination of chiral trans-3-acetyl-4-alkylpyrrolidin-2-ones

G. Mobbili, R. Galeazzi, M. Orena, 2003 .

A Simple and Practical Method for Tetrahydropyranylation of Alcohols and Phenols

A. Bongini, G. Cardillo, M. Orena, 1979 .

THERMODYNAMIC VS. KINETIC CONTROL IN THE STEREOSELECTIVE INTRAMOLECULAR CONJUGATE ADDITION OF AMIDE ENOLATES LEADING TO CHIRAL TRANS-3,4-DISUBSTITUTED PYRROLIDIN-2-ONES

G. Mobbili, R. Galeazzi, M. Orena, 1999 .

STEREOSELECTIVE REDUCTION OF CHIRAL TRANS-3-ACETYL-4-ALKYLPYRROLIDIN-2-ONES

G. Mobbili, R. Galeazzi, S. Geremia, 1999 .

A convenient approach to diastereomerically pure 1,3,4-trisubstituted pyrrolidin-2-ones by intramolecular cyclisation of N-(2-alken-1-yl)amides mediated by Mn(III). An entry to both (R)- and (S)-3-pyrrolidineacetic acid

G. Mobbili, R. Galeazzi, M. Orena, 1996 .

Stereoselective iodocyclisation of 3-acylamino-2-methylene alkanoates: a computational insight

G. Mobbili, S. Rinaldi, R. Galeazzi, 2006 .

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 .

Synthesis of chiral oxazolidin-2-ones from N-alkoxycarbonyl amino epoxides: a computational studyElectronic supplementary information (ESI) available: structures of localized transition states. See http://www.rsc.org/suppdata/p1/b2/b203702e/

M. E. González-Rosende, R. Galeazzi, M. Orena, 2002 .

Polymer supported reagents. Chromic acid on anion exchange resins. A simple and practical oxidation of alcohols to aldehydes and ketones

G. Cardillo, M. Orena, S. Sandri, 1976 .

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 .

Factors affecting the regioselection of allylic imidate iodocyclization

A. Bongini, C. Tomasini, G. Cardillo, 1986 .

Chiral 3-hydroxypyrrolidin-2-ones from a Baylis–Hillman adduct: convergent, stereoselective synthesis of a glycosidase inhibitor

G. Mobbili, S. Rinaldi, R. Galeazzi, 2004 .

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

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

Stereoselective iodocyclization of 3-acylamino-2-methylene alkanoates: synthesis of analogues of N-benzoyl-syn-phenylisoserine.

G. Mobbili, S. Rinaldi, R. Galeazzi, 2004, Organic letters.

Synthesis of chiral 1,2-diamines

Elena Bruni, C. Tomasini, G. Cardillo, 1989 .

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

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

Analogues of both Leu- and Met-enkephalin containing a constrained dipeptide isostere prepared from a Baylis-Hillman adduct

S. Rinaldi, R. Galeazzi, G. Martelli, 2010, Amino Acids.

Diastereoselective alkylation of 3-acylimidazolidin-2-ones: synthesis of (R)- and (S)-lavandulol

G. Cardillo, M. Orena, S. Sandri, 1988 .

Straightforward Synthesis of (R,S)-β-Methyleneaspartic Acid, an Inhibitor of Glutamate-Aspartate Transaminase

S. Rinaldi, R. Galeazzi, G. Martelli, 2006 .

From pyrrolidin-2-ones to 3-aza-2-oxobicyclo[3.2.0]heptanes. Synthesis of both enantiomers of cis-2-aminomethylcyclobutane carboxylic acid, a conformationally restricted analogue of GABA

G. Mobbili, R. Galeazzi, M. Orena, 1999 .

Chiral 3-hydroxypyrrolidin-2-ones. Part 2: Stereodivergent synthesis of conformationally restricted analogues of β-homoserine

S. Rinaldi, R. Galeazzi, G. Martelli, 2005 .

A new approach to 2-phenylthioalcohols in high optical purity

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

Synthesis of unsaturated β-amino acid derivatives from carbamates of the Baylis–Hillman products

R. Galeazzi, M. Orena, J. Sepúlveda-Arques, 2002 .

A short approach to chaetomellic anhydride A from 2,2-dichloropalmitic acid : elucidation of the mechanism governing the functional rearrangement of the chlorinated pyrrolidin-2-one intermediate

A. Mucci, R. Galeazzi, C. Danieli, 2006 .

Cyclisation of (R)- and (S)-N-allyl-N-(1-phenylethyl) methoxycarbonylacetamide mediated by Mn(III): Preparation and structural assignment of 3-aza-2-oxobicyclo[3.1.0]hexanes

G. Mobbili, R. Galeazzi, S. Geremia, 1996 .

An efficient synthesis of (R)-(+)- and (S)-(-)-propranolol from resolved 5-idomethyloxazo-lidin-2-ones

C. Tomasini, G. Cardillo, M. Orena, 1987 .

From 3-aza-2-oxobicyclo[3.1.0]hexane to enantiopure disubstituted cyclopropane: a convenient approach to cis-2,3-methano-GABA

G. Mobbili, R. Galeazzi, M. Orena, 1997 .

Stereocontrolled reactions through heterocyclic intermediates

G. Cardillo, M. Orena, S. Sandri, 1988 .

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 .

Iodocyclofunctionalization of (Z)-1-trichloroacetimidoyloxyalk-2-enes and 3-trichloroacetimidoyloxyalk-1-enes. Synthesis of (±)-erythro-sphinganine triacetate and (±)-threo-sphinganine triacetate

A. Bongini, C. Tomasini, G. Cardillo, 1986 .

A new approach to (±)-2-amino-2-deoxytetritol derivatives

A. Bongini, C. Tomasini, G. Cardillo, 1985 .

Regio- and stereoselective synthesis of methyl .alpha.-L-daunosaminide hydrochloride

C. Tomasini, G. Cardillo, M. Orena, 1984 .

A regio- and stereoselective synthesis of methyl α-L-ristosaminide hydrochloride

A. Bongini, C. Tomasini, G. Cardillo, 1983 .

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 .

Stereodivergent Baylis-Hillman Reaction of a Chiral Acryloyl Imide Exploiting Ion-Chelation Effect: Mechanistic Insight on the Rearrangement of Trichloroacetimidates of the Baylis-Hillman Adducts to Trichloroacetamides

S. Rinaldi, G. Martelli, M. Orena, 2007 .

Conformationally restricted analogues of both (S)-β-homoserine and (S)-aspartic acid from chiral 3-acylamino pyrrolidin-2-ones

S. Rinaldi, P. Sabatino, R. Galeazzi, 2005 .

α-Methylene-β-trichloroacetylamino alkanoates from trichloroacetimidates of the Baylis-Hillman adducts

S. Rinaldi, R. Galeazzi, G. Martelli, 2004 .

Enantiopure Derivatives of Aza-Baylis-Hillman Adducts by Subsequent SN′-SN′ Reactions of Acylcarbamates Bearing a Chiral Auxiliary

S. Rinaldi, G. Martelli, M. Orena, 2009, Molecules.

A new approach to the synthesis of enantiomerically pure 2,3-diaminoacids through chiral imidazolidin-2-ones

C. Tomasini, G. Cardillo, M. Orena, 1991 .

Synthesis and Structural Assignment of Diastereomerically Pure N-Substituted 4-Alkylpyrrolidin-2-ones, Intermediates for the Preparation of 3-Alkylpyrrolidines in Both Enantiomerically Pure Forms

G. Mobbili, R. Galeazzi, M. Orena, 1994 .

A novel, efficient synthesis of (±)-erythro-sphingosine

C. Tomasini, G. Cardillo, M. Orena, 1986 .

Diastereoselective functionalisation of Baylis–Hillman adducts: a convenient approach to α-methyl-α-amino acids

S. Rinaldi, P. Sabatino, G. Martelli, 2010, Amino Acids.

Simple amphiphilic α-hydrazido acids: Rational design, synthesis, and in vitro bioactivity profile of a novel class of potential antimicrobial compounds.

S. Rinaldi, M. Orena, F. Biavasco, 2020, European journal of medicinal chemistry.

Synthesis and structural characterisation as 12-helix of the hexamer of a beta-amino acid tethered to a pyrrolidin-2-one ring.

S. Mammi, S. Rinaldi, R. Galeazzi, 2006, Chemical communications.

Synthesis of Enantiopure Isosteres of Amino Acids Containing a Quaternary Stereocenter: Experimental and Computational Evaluation of a Novel Class of Atropisomers

S. Rinaldi, F. Piccinelli, A. Amici, 2018, European Journal of Organic Chemistry.

Highly stable atropisomers by electrophilic amination of a chiral γ-lactam within the synthesis of an elusive conformationally restricted analogue of α-methylhomoserine

S. Rinaldi, M. Orena, A. Tolomelli, 2016, Amino Acids.

β-Peptoids: synthesis of a novel dimer having a fully extended conformation

S. Rinaldi, C. Tomasini, G. Martelli, 2012, Amino Acids.

Novel nucleoside analogs tethered on (3R,4R)-4-(hydroxymethyl)pyrrolidin-3-ol

S. Rinaldi, A. Amici, G. Martelli, 2015, Journal of the Iranian Chemical Society.

Synthesis of Enantiomerically Pure 3‐Amino‐2‐methylenealkanoates (Aza‐Morita–Baylis–Hillman Adducts) Mediated by Cinchona Alkaloids

S. Rinaldi, G. Martelli, M. Orena, 2011 .

Analogues of nucleosides: synthesis of chiral pyrrolidin-2-ones or pyrrolidines-bearing nucleobases

S. Rinaldi, G. Martelli, M. Orena, 2014, Monatshefte für Chemie - Chemical Monthly.

Chromate ion as a synthetically useful nucleophile: a novel synthesis of aldehydes from alkyl halides

G. Cardillo, M. Orena, S. Sandri, 1976 .

Synthesis of compounds containing the isoprene unit : A stereospecific synthesis of dehydronerol isovalerate, a component of anthemis Montana L

G. Cardillo, M. Orena, S. Sandri, 1976 .

POLYMER SUPPORTED REAGENTS. CHROMIC ACID ON ANION EXCHANGE RESIN. SYNTHESIS OF ALDEHYDES AND KETONES FROM ALLYLIC AND BENZYLIC HALIDES

G. Cardillo, M. Orena, Serlio Sandri, 1976 .

Conjugate intra- and intermolecular addition mediated by methoxide anion on polymeric support

R. Galeazzi, M. Orena, Cristiana Fava, 2000 .

Novel enantiomerically pure 2-amino-1,4-diols from chiral 4-hydroxymethyl-5-iodo-1,3-oxazin-2-ones

M. E. González-Rosende, M. Orena, J. Sepúlveda-Arques, 2004 .

1,3-Oxazin-2-ones vs tetrahydrofurans by iodocyclisation of 2-alkoxycarbonylamino-3-alken-1-ols

M. E. González-Rosende, R. Galeazzi, Patricia Cava-Montesinos, 2000 .

Highly regio- and stereoselective iodocyclization of chiral 3-alkoxycarbonyl-4-propenyl-2,2-dimethyl-1,3-oxazolidines: a computational investigation

M. E. González-Rosende, R. Galeazzi, M. Orena, 1999 .

Homochiral oxazolidin-2-ones and imidazolidin-2-ones by tandem nucleophilic addition-conjugate addition

M. E. González-Rosende, R. Galeazzi, M. Orena, 2004 .

A new synthetic approach to 3-amino-1,2-diols from allylic alcohols via trichloroacetimidates

G. Cardillo, M. Orena, S. Sandri, 1984 .

Synthesis of oxazolidin-2-ones using carbonate ion on a polymeric support

C. Tomasini, G. Cardillo, M. Orena, 1985 .

Synthesis of (R)-N-Tosylemeriamine via Chiral N-Tosylimidazolidin-2-ones

C. Tomasini, G. Cardillo, M. Orena, 1990 .

Oxazolidin-2-ones from allylic amines by means of iodine and carbonate anion on polymeric support. A convenient synthesis of (.+-.)-propranolol

G. Cardillo, M. Orena, S. Sandri, 1986 .

Oxazolidin-2-ones from Allylic Amines by Means of Iodine and Carbonate Anion on Polymeric Support.

G. Cardillo, M. Orena, S. Sandri, 1986 .

Oxidation of Alcohols with Chromium Trioxide in Hexamethylphosphoric Triamide

G. Cardillo, M. Orena, S. Sandri, 1976 .

Synthesis, conformation and biological activity of linear and cyclic Thr6‐bradykinin analogues containing N‐benzylglycine in place of phenylalanine

T. Piek, M. Gobbo, R. Galeazzi, 2001, Journal of peptide science : an official publication of the European Peptide Society.

A New Conformationally Restricted Mimetic of Dipeptide EG – Synthesis of an Analogue of FEG

G. Mobbili, S. Rinaldi, R. Galeazzi, 2007 .

Polymer Supported Reagents. The Use of Anion Exchange Resins in the Synthesis of Sulfones

M. Orena, D. Savoia, F. Manescalchi, 1979 .

Stereoelectronic properties and activity of some imidazolinone herbicides: a computational approach☆

R. Galeazzi, C. Zadra, M. Orena, 2003 .

Molecular structure and stereoelectronic properties of herbicide sulphonylureas.

R. Galeazzi, C. Zadra, M. Orena, 2002, Bioorganic & medicinal chemistry.

Modeling and Synthesis of Conformationally Restricted Amino Acids

G. Mobbili, R. Galeazzi, M. Orena, 2004 .

Highly stable atropisomers by electrophilic amination of a chiral γ-lactam within the synthesis of an elusive conformationally restricted analogue of α-methylhomoserine

S. Rinaldi, A. Amici, M. Orena, 2016, Amino Acids.

Synthesis of a cyclic isostere of α-methyl homoserine by a stereoselective acylation–alkylation sequence of a chiral γ-lactam

S. Rinaldi, G. Martelli, M. Orena, 2014, Amino Acids.

Diastereoselective hetero-diels-alder cycloaddition of a C-nitroso compound prepared starting from a homochiral imidazolidin-2-one

G. Mobbili, R. Galeazzi, M. Orena, 1994 .

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

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

Stereoselective alkylation of chiral pyrrolidin-2-ones leading to novel conformationally restricted analogues of 3-methylaspartic acid: a computational investigation

S. Rinaldi, R. Galeazzi, G. Martelli, 2012, Monatshefte für Chemie - Chemical Monthly.

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 .

Synthesis of a versatile constrained analogue of dipeptide DG (Asp-Gly)

S. Rinaldi, R. Galeazzi, G. Martelli, 2008, Amino Acids.

Recent Advances in Chemistry of γ-Lactams: Part II. Functionalization by C-C or CHeteroatom Bond Formation

S. Rinaldi, G. Martelli, M. Orena, 2014 .

Recent Advances in Chemistry of γ-Lactams. Part 1. Synthesis Starting from Acyclic or Cyclic Precursors

S. Rinaldi, G. Martelli, M. Orena, 2014 .

β-Peptoids: synthesis of a novel dimer having a fully extended conformation

S. Rinaldi, C. Tomasini, G. Martelli, 2012, Amino Acids.

Imidazolidinone-Tethered α-Hydrazidopeptides - Synthesis and Conformational Investigation

S. Rinaldi, M. Calvaresi, G. Martelli, 2019, Annalen der Pharmacie.

Synthesis of a cyclic isostere of α-methyl homoserine by a stereoselective acylation–alkylation sequence of a chiral γ-lactam

S. Rinaldi, G. Martelli, M. Orena, 2014, Amino Acids.