G. Pollini

发表

Synthetic routes to chiral nonracemic and racemic dihydro- and tetrahydrothiophenes.

S. Benetti, C. De Risi, G. Pollini, 2012, Chemical reviews.

Convenient ‘one-pot’ synthesis of 3,4-substituted tetrahydrothiophenes through tandem Michael–Henry and Michael–Michael reactions

S. Benetti, G. Pollini, A. Barco, 2006 .

Arecoline tripeptide inhibitors of proteasome.

A. Canella, R. Gavioli, G. Pollini, 2004, Journal of medicinal chemistry.

Proteasome inhibitors: synthesis and activity of arecoline oxide tripeptide derivatives

A. Canella, C. De Risi, G. Pollini, 2004 .

Recent Developments in General Methodologies for the Synthesis of α-Ketoamides.

C. De Risi, G. Pollini, V. Zanirato, 2016, Chemical reviews.

Synthetic prostaglandin1 analogue: in vitro studies on human neutrophils.

E. Vicenzi, G. Pollini, A. Barco, 1982, Immunopharmacology.

4-[(4-Methylphenyl)sulfonyl]-1-(triphenylphosphoranylidene)-2-butanone as a convenient precursor for a new formal synthesis of KDO

V. Bertolasi, S. Benetti, G. Pollini, 2002 .

Polymer-bound 4-benzylsulfonyl-1-triphenylphosphoranylidene-2-butanone as a tool for the solid-phase synthesis of substituted piperidin-4-one derivatives.

S. Benetti, G. Pollini, V. Zanirato, 1998 .

Formal synthesis of (±)-Ambrox®

S. Benetti, G. Pollini, A. Barco, 1995 .

A new simple route for the synthesis of (±)-2-azetidinones starting from β-enaminoketoesters

V. Bertolasi, G. Pollini, C. D. Risi, 1999 .

4‐[(4′‐Methylphenyl)sulfonyl]‐1‐(triphenylphosphoranylidene)‐2‐butanone as a New Four‐Carbon Synthon for Substituted Divinyl Ketones

S. Benetti, G. Pollini, V. Zanirato, 2001 .

Total synthesis of (±)-epibatidine

R. Romagnoli, S. Benetti, G. Pollini, 1994 .

Tetramethylguanidine-Catalyzed Addition of Nitromethane to α,β-Unsaturated Carboxylic Acid Esters

G. Pollini, A. Barco, G. D. Giuli, 1972 .

Regio - and enantioselective bioreduction of ethyl 2,4-dioxoalkanoates and γ-Keto-α-enamino esters with fermenting baker's yeast

S. Manfredini, P. Baraldi, R. Romagnoli, 1992 .

Efficient synthesis and biological evaluation of two modafinil analogues.

L. Ferraro, S. Tanganelli, C. De Risi, 2008, Bioorganic & medicinal chemistry.

Ethyl 2,4-dioxoalkanoates as starting materials for a convenient route to 3(2H) furanones and 3(2H) furanimines

S. Manfredini, P. Baraldi, S. Benetti, 1987 .

Ethyl 5-substituted-3-isoxazolecarboxylates as starting materials for a convenient route to 3(2H)furanones and 3(2H)iminofuranes.

S. Manfredini, P. Baraldi, S. Benetti, 1984 .

From (−)-quinic acid to 8-azabicyclo[3.2.1]octane framework: Preparation of an enantiopure tropan-6α-ol

S. Benetti, G. Pollini, V. Zanirato, 1999 .

4-[(4-Methylphenyl)sulfonyl]-1-(triphenylphosphoranylidene)-2-butanone and its dianion as versatile tools in organic synthesis

S. Benetti, G. Pollini, V. Zanirato, 1998 .

Tetramethylguanidine (TMG)-catalyzed addition of dialkyl phosphites to α,β-unsaturated carbonyl compounds, alkenenitriles, aldehydes, ketones and imines

I. Lampronti, M. Roberti, G. Pollini, 1998 .

4‐Methoxycarbonylthiolan‐3‐one

S. Benetti, G. Pollini, A. Barco, 2001 .

The intramolecular nitrile oxide cycloaddition route to forskolin

P. Baraldi, S. Benetti, G. Pollini, 1986 .

A New and Expedient Diastereoselective Synthesis of α‐(Hydroxyamino)phosphonates and α‐Aminophosphonates by Silyl Triflate Promoted Diethyl Phosphite Addition to Chiral N‐Benzyl Nitrones

V. Bertolasi, D. Perrone, G. Pollini, 2003 .

O-Silyl triflate-promoted addition of diethyl phosphite to chiral aldonitrones. A rapid access to complex α-amino phosphonates and their N-hydroxy derivatives

D. Perrone, G. Pollini, C. D. Risi, 2001 .

A simple entry to chiral non-racemic 2-piperazinone derivatives

S. Benetti, G. Pollini, V. Zanirato, 2005 .

4-[(4-Methylphenyl)sulfonyl]-1-(triphenylphosphoranylidene)-2-butanone and Its Dianion as Versatile Tools in Organic Synthesis.

S. Benetti, G. Pollini, V. Zanirato, 1998 .

A [3+2]nitrile oxide cycloaddition approach to (−)-pyrenophorin, and rosefuran

S. Benetti, G. Pollini, V. Zanirato, 1995 .

Enantioselective synthesis of (−)-meroquinene through tandem Michael reaction methodology.

G. Spalluto, R. Romagnoli, S. Benetti, 1994 .

Synthesis of 1-Phthalimidoalkanephosphonates

P. Baraldi, G. Pollini, D. Simoni, 1982 .

Tetramethylguanidine (TMG)‐Catalyzed Addition of Dialkyl Phosphites to α,β‐Unsaturated Carbonyl Compounds, Alkenenitriles, Aldehydes, Ketones and Imines.

I. Lampronti, M. Roberti, G. Pollini, 1998 .

Facile synthesis of 2-nitroalkanols by tetramethylguanidine (TMG)-catalyzed addition of primary nitroalkanes to aldehydes and alicyclic ketones

I. Lampronti, S. Manfredini, M. Roberti, 1997 .

Diastereoselective synthesis of β-amino-α-hydroxy phosphonates via oxazaborolidine catalyzed reduction of β-phthalimido-α-keto phosphonates

S. Benetti, G. Pollini, V. Zanirato, 1999 .

Recent advances in the stereoselective synthesis of trans-3,4-disubstituted-piperidines : applications to (-)-paroxetine

C. Trapella, G. Pollini, V. Zanirato, 2008 .

Synthetic approaches to enantiomerically pure 8-azabicyclo[3.2.1]octane derivatives.

S. Benetti, C. De Risi, G. Pollini, 2006, Chemical reviews.

Tandem michael reactions for the construction of pyrrolidine and piperidine ring systems

G. Spalluto, S. Benetti, G. Pollini, 1990 .

Enantioselective synthesis of (+)- and (−)-α-allokainic acid

G. Spalluto, S. Benetti, G. Pollini, 1990 .

Enantioselective Formal Synthesis of Acromelic Acid A via Tandem Michael Reaction Methodology.

G. Spalluto, S. Benetti, G. Pollini, 1993 .

Generation and cycloaddition reactions of 3-substituted-2-nitro-1,3-dienes

G. Spalluto, S. Benetti, G. Pollini, 1991 .

Synthesis of natural products via isoxazoles

P. Baraldi, S. Benetti, G. Pollini, 1987 .

Methyl 4-oxothiolane-3-carboxylate and methyl 2-methyl-4-oxothiolane-3-carboxylate anions as synthetic equivalents of α-acrylate and α-crotonate anions. Formal synthesis of integerrinecic acid

P. Baraldi, S. Benetti, G. Pollini, 1985 .

A new ‘one-pot’ synthesis of 2-substituted 3-nitro pyrrolidines through a multicomponent domino reaction

S. Benetti, G. Pollini, Nikla Baricordi, 2004 .

D-(−)-Quinic acid: a chiron store for natural product synthesis

S. Benetti, G. Pollini, V. Zanirato, 1997 .

A novel α-acrylate anion equivalent: a useful synthon for α-substituted acrylic esters

P. Baraldi, S. Benetti, G. Pollini, 1983 .

Synthesis of (±)15-Hydroxy-Prosta-2, 4, 8(12), 13-Tetraen-1-Oic Acid Methyl Esters

P. Baraldi, S. Benetti, G. Pollini, 1977 .

Synthesis of 3-Substituted 7-Methyl-5H-pyrazole[4,3-d]-1,2,3-triazin- 4(3H)-ones and Amide-N-Substituted 3-Methyl-4-diazopyrazole-5-carboxamides

S. Manfredini, P. Baraldi, G. Pollini, 1988 .

A CHEMOENZYMATIC APPROACH TO CHIRAL PHENYLISOSERINATES USING 4-ISOPROPYL-2-OXAZOLIN-5-ONE AS MASKED UMPOLED SYNTHON FOR HYDROXYCARBONYL ANION

R. Romagnoli, S. Benetti, G. Pollini, 1994 .

Diastereoselective synthesis of 2-substituted-piperidin-4-ones as convenient precursors for an asymmetric approach to carbacephams

S. Benetti, G. Pollini, A. Barco, 2003 .

Mastering chiral substituted 2-oxopiperazines

C. Trapella, G. Pollini, V. Zanirato, 2010 .

A unified asymmetric approach to substituted hexahydroazepine and 7-azabicyclo[2.2.1]heptane ring systems from D(−)-quinic acid: Application to the formal synthesis of (−)-balanol and (−)-epibatidine

S. Benetti, G. Pollini, V. Zanirato, 1997 .

A new approach to kainoids through tandem Michael reaction methodology: application to the enantioselective synthesis of (+)- and (-)-.alpha.-allokainic acid and to the formal synthesis of (-)-.alpha.-kainic acid

G. Spalluto, S. Benetti, G. Pollini, 1992 .

Enantioselective approach to 7-azabicyclo[2.2.1]heptane ring systems using D-(−)-quinic acid as the chiral educt: Application to the formal synthesis of (+)-epibatidine

S. Benetti, G. Pollini, V. Zanirato, 1997 .

A new enantioselective route to kainoids: application to the formal synthesis of (–)-α-kainic acid

G. Spalluto, S. Benetti, G. Pollini, 1991 .

A [3+2] nitrile oxide cycloaddition approach to retinoids

S. Manfredini, P. Baraldi, S. Benetti, 1988 .

Synthesis and reactivity of a stable precursor of 2-cyano-1,3-butadiene

S. Manfredini, P. Baraldi, S. Benetti, 1988 .

Hagemann's ester: a timeless building block for natural product synthesis

S. Benetti, G. Pollini, V. Zanirato, 2010 .

An efficient approach to chiral nonracemic trans- and cis-decalin scaffolds for drimane and labdane synthesis

V. Bertolasi, G. Pollini, V. Zanirato, 2004 .

A Facile Alkylation of Ethyl 2-Oxocyclopentanecarboxylate

S. Benetti, G. Pollini, A. Barco, 1973 .

Synthesis of Natural Products via Isoxazoles

P. Baraldi, S. Benetti, G. Pollini, 1988 .

A new, elegant route to a key intermediate for the synthesis of 9(0)-methanoprostacyclin

P. Baraldi, S. Benetti, G. Pollini, 1980 .

Azaprostaglandin analogues. Synthesis and biological properties of 11-azaprostaglandin derivatives.

P. Baraldi, S. Benetti, G. Pollini, 1981, Journal of medicinal chemistry.

Active γ-Manganese Dioxide Promoted Conversion of 4,5-Dihydro-1,2-oxazoles to 1,2-Oxazoles

P. Baraldi, S. Benetti, G. Pollini, 1977 .

1,4-Diketones via isoxazole intermediates

P. Baraldi, S. Benetti, G. Pollini, 1979 .

SYNTHESIS OF AN 11-DEOXY-8-AZAPROSTAGLANDIN E1 INTERMEDIATE

P. Baraldi, S. Benetti, G. Pollini, 1979 .

Synthesis of 14-Hydroxy-8-Azaprostanoic Acids Methyl Ester

P. Baraldi, S. Benetti, G. Pollini, 1978 .

Synthesis of biomimetic light-driven molecular switches via a cyclopropyl ring-opening/nitrilium ion ring-closing tandem reaction

M. Olivucci, G. Pollini, V. Zanirato, 2007 .

1,4-Dithiane-2,5-diol as an efficient synthon for a straightforward synthesis of functionalized tetrahydrothiophenes via sulfa-Michael/aldol-type reactions with electrophilic alkenes

V. Bertolasi, S. Benetti, G. Pollini, 2012 .

Synthesis of melodienone and 7-hydroxy-6-hydromelodienone, two heptenes from Melodorum fruticosum

R. Romagnoli, S. Benetti, G. Pollini, 1994 .

A new enantiodivergent synthesis of the Geissman–Waiss lactone

S. Benetti, G. Pollini, V. Zanirato, 2007 .

Synthetic studies towards forskolin

P. Baraldi, V. Ferretti, S. Benetti, 1989 .

The Intramolecular Nitrile Oxide Cycloaddition Route to Forskolin.

P. Baraldi, S. Benetti, G. Pollini, 1986 .

4-Isopropyl-2-oxazolin-5-one anion as masked umpoled synthon for both formyl and hydroxycarbonyl anions: Generation, reactivity and synthetic applications

G. Spalluto, S. Benetti, G. Pollini, 1996 .

Protection by pyroglutamic acid and some of its newly synthesized derivatives against glutamate-induced seizures in mice.

S. Manfredini, L. Beani, G. Pollini, 1990, Arzneimittel-Forschung.

Enantiodivergent synthesis of 2-hydroxymethyl-3-hydroxy-4-nitro-pyrrolidines through tandem Michael-Henry reaction using L-serine as the chiral educt

R. Romagnoli, S. Benetti, G. Pollini, 1996 .

The Use of Phase-Transfer Catalysis for theN-Alkylation of Indole

P. Baraldi, S. Benetti, G. Pollini, 1976 .

Stereoselective Synthesis of 8-Aza-9,11-ethenoprostaglandin H1

P. Baraldi, S. Benetti, G. Pollini, 1982 .

Synthesis of syn- and anti-tricyclo [4.1.0.02,4] heptan-5-ones and related compounds

P. Baraldi, S. Benetti, G. Pollini, 1984 .

Enantioselective formal synthesis of (-)-ovalicin using quinic acid as a chiral template 1 Keywords:

S. Benetti, G. Pollini, V. Zanirato, 1998 .

Synthesis and prostaglandin-like activity of 2-(trans-3-hydroxy-1-octenyl)-3-indoleheptanoic acid.

P. Baraldi, S. Benetti, G. Pollini, 1978, Journal of medicinal chemistry.

3,4-Bismethylenecyclopentanone ethylene ketal: A useful diene for[6.5]ring systems: Application to a formal synthesis of gibberellic acid

S. Manfredini, S. Benetti, G. Pollini, 1989 .

Trapping of cyclopentadienone as a 4π component in Diels–Alder reactions with ethyl acrylate: a simple synthesis of (±)-sarkomycin

P. Baraldi, S. Benetti, G. Pollini, 1984 .

Stereospecific nitromethane conjugate addition to 4-oxygenated-2-substituted-cyclo pent-2-enones: a simple approach to prostaglandins

P. Baraldi, S. Benetti, G. Pollini, 1987 .

A new simple synthesis of α-substituted acrylonitriles

P. Baraldi, S. Benetti, G. Pollini, 1985 .

Synthesis of 2,5-Disubstituted Pyrroles and Pyrrolidines by Intramolecular Cyclization of 6-Amino-3-keto Sulfones

S. Benetti, G. Pollini, V. Zanirato, 2002 .

A convenient preparation of 3-isopropyl-1-methylcyclopentylmethanol and 1-isopropyl-3-methylcyclopentylmethanol via Favorskii rearrangement

S. Benetti, G. Pollini, V. Zanirato, 2009 .

Elaboration of the .omega.-chain of 11-deoxyprostanoid derivatives through isoxazole intermediates

P. Baraldi, S. Benetti, G. Pollini, 1981 .

SYNTHESIS OF cis-4-OCTENE-1,8-DIOIC ACID AND ITS ESTERS

S. Benetti, G. Pollini, A. Barco, 1974 .

Application of (3 + 2)Nitrile Oxide Cycloaddition Chemistry to the Construction of Retinoid Skeleton and to a New Formal Synthesis of (.+‐ .)‐Ascofuranone and Geiparvarin.

S. Manfredini, P. Baraldi, G. Pollini, 1994 .

Enantioselective synthesis of the hexahydronaphthalene nucleus of (−)-compactin from ethyl (1R,2S)-2-methyl-4-oxocyclohexanecarboxylate and 2-(3-nitropropyl)-1,3-dioxolane as four carbon bifunctional annelating agent.

G. Spalluto, R. Romagnoli, S. Benetti, 1994 .

Enantioselective Synthesis of the Hexahydronaphthalene Nucleus (XIII) of (‐)‐Compactin from Ethyl (1R,2S)‐2‐Methyl‐4‐ oxocyclohexanecarboxylate and 2‐(3‐Nitropropyl)‐1,3‐dioxolane as Four‐ Carbon Bifunctional Annelating Agent.

G. Spalluto, R. Romagnoli, S. Benetti, 2010 .

A Diphenylprolinol TMS Ether/Bile Acid Organocatalytic System for the Asymmetric Domino Sulfa-Michael/Aldol Condensation Reactions of 1,4-Dithiane-2,5-diol and Cinnamaldehydes

S. Benetti, G. Pollini, V. Zanirato, 2009 .

A formal total synthesis of (±)-forskolin through [3 + 2] nitrile oxide cycloaddition chemistry

G. Spalluto, P. Baraldi, S. Benetti, 1991 .

The Use of Phase-Transfer Catalysis for the N-Alkylation of Indole

P. Baraldi, S. Benetti, G. Pollini, 1976 .

Enantioselective approach to tropane skeleton: Synthesis of (1S, 5S, 6R)-6-hydroxy-8-methyl-8-azabicyclo[3.2.1]octan-3-one

G. Pollini, V. Zanirato, C. D. Risi, 2004 .

3,5-Disubstituted isoxazoles as a latent aldol moiety: application to the synthesis of (±)-[6]-gingerol

P. Baraldi, S. Benetti, G. Pollini, 1981 .

3,5-Disubstituted isoxazoles as synthons for (.+-.)-pyrenophorin and (.+-.)-vermiculine synthesis

P. Baraldi, S. Benetti, G. Pollini, 1983 .