Giovanni Palumbo | Università degli Studi di Napoli "Federico II" (original) (raw)

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Papers by Giovanni Palumbo

Research paper thumbnail of Asymmetric induction in the coupling of 5,6-dihydro-1,4-dithiins with chiral aldehydes. A new synthetic approach to polyhydroxylated compounds

Tetrahedron, 1996

A new strategy is designed to synthesize polyhydroxyl compounds (and/or carbohydrates) by couplin... more A new strategy is designed to synthesize polyhydroxyl compounds (and/or carbohydrates) by coupling of 5, 6-dihydro-1, 4-dithiins-carrying a vinylic hydrogen atom-with chiral aldehydes and, in sequence, stereoselective removal of the dithiodimethylene dithiin ...

Research paper thumbnail of A Stereoconvergent Tsuji–Trost Reaction in the Synthesis of Cyclohexenyl Nucleosides

Chemistry – A European Journal, 2020

(D.D.). Supporting information for this article is given via a link at the end of the document.

Research paper thumbnail of ChemInform Abstract: A One-Step Synthesis of 2,3-Dihydro-1,4-benzothiazines and Phenothiazines from 1,3-Thiazolidine Derivatives of Cyclohexanones

Research paper thumbnail of A view from space. Monitoring and management for World Heritage Sites

NASA and The Getty Conservation Institute are conducting an experiment in the application of remo... more NASA and The Getty Conservation Institute are conducting an experiment in the application of remotely sensed multispectral and radar data for monitoring change at World Heritage Sites. The project is concerned both with the principles of this approach and with current limitations. The latter have clearly demonstrated that automatic monitoring cannot be easily achieved, due to problems of low resolution, lack of repeatability, and cost, but the integration of this remotely sensed data with other data types into a geographic data management system may provide a monitoring management tool that can be used to test the potential of a fully integrated approach to site definition, monitoring, and management. The test case being adopted covers the area of Chaco Culture National Historic Park, in New Mexico, USA, a major Anasazi complex which is registered in the UNESCO’s World Heritage List. Data assembled included a variety of remotely-sensed information, GPS surveys, and the preparation o...

Research paper thumbnail of N-Butyl-L-Deoxynojirimycin (L-NBDNJ): Synthesis of an Allosteric Enhancer of α-Glucosidase Activity for the Treatment of Pompe Disease

Journal of medicinal chemistry, Jan 7, 2017

The highly stereocontrolled de novo synthesis of L-NBDNJ (the unnatural enantiomer of the iminosu... more The highly stereocontrolled de novo synthesis of L-NBDNJ (the unnatural enantiomer of the iminosugar drug Miglustat) and a preliminary evaluation of its chaperoning potential are herein reported. L-NBDNJ is able to enhance lysosomal α-glucosidase levels in Pompe disease fibroblasts, either when administered singularly or when co-incubated with the recombinant human α-glucosidase. In addition, differently from its D-enantiomer, L-NBDNJ does not act as a glycosidase inhibitor.

Research paper thumbnail of ChemInform Abstract: Asymmetric Synthesis of Optically Active Phthalides via ortho- Lithiation and Cyclization of Chiral N-Monosubstituted Benzamides

Research paper thumbnail of Synthesis of C-Protected 2,2-Dideutero � 3 -Amino Acids

Synthesis Stuttgart, 2006

Research paper thumbnail of Rapid access to 1,6-anhydro-beta-L-hexopyranose derivatives via domino reaction: Synthesis of L-allose and L-glucose

The Journal of Organic Chemistry, Aug 1, 2008

An expeditious and efficient synthesis of 1,6-anhydro-beta-L-hexopyranosyl derivatives 3 as valua... more An expeditious and efficient synthesis of 1,6-anhydro-beta-L-hexopyranosyl derivatives 3 as valuable building blocks for the preparation of L-sugars is herein reported. This route relies upon the use of a domino reaction involving five synthetic steps from the 5,6-dihydro-1,4-dithiin 4. As 1,6-anhydro derivatives 3 are obtained, dithioethylene bridge removal and double-bond dihydroxylation give access to protected L-allose and L-glucose in stereoselective fashion and high yields.

Research paper thumbnail of �-Amino-a-hydroxy Esters by Asymmetric Hydroxylation ofhomo-�-Amino Acid Esters

Research paper thumbnail of Reactivity of Ethanediyl S,S -Acetals; 2. Synthesis of 2,3-Dihydro-1,4-dithiins

Synthesis Stuttgart, 1991

Research paper thumbnail of Chemistry of Ethanediyl S,S-Acetals 9-Asymmetric Synthesis of Chiral cis Allylic Alcohols

Http Dx Doi Org 10 1080 00397919508011763, Sep 23, 2006

Research paper thumbnail of Synthesis of c-protected 2,2-dideutero β3-amino acids

Research paper thumbnail of Reactivity of Ethanediyl S,S-Acetals. Part 3. Ring Aromatization in Cyclohexanone Derivatives: A Novelty Synthesis of 1,4-Benzodithians

Research paper thumbnail of Mild Synthesis of Protected a-D-Glycosyl Iodides

Research paper thumbnail of ChemInform Abstract: Chemistry of Ethandiyl S,S-Acetals. Part 13. Aromatic Ring Bromination in 1,4-Benzothiazines, 1,4-Benzoxathianes and 1,4-Benzodithianes: The Occurrence of Vicarious Nucleophilic Substitution of Hydrogen and Electrophilic Aromatic Subs

Cheminform, 2010

ABSTRACT ChemInform is a weekly Abstracting Service, delivering concise information at a glance t... more ABSTRACT ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

Research paper thumbnail of A New Three Carbon Homologation Via Sulfur Containing Heterocyclic Systems

Phosphor Sulfur Silicon, 1999

A new reagent, based on a 5,6-dihydro-1,4-dithiin heterocyclic system, has been devised and conve... more A new reagent, based on a 5,6-dihydro-1,4-dithiin heterocyclic system, has been devised and conveniently used for 3 carbon elongations of various electrophiles. In fact, it acts as either a propenyl alcohol or an acrolein anion equivalent, introducing into the new molecule a moiety consisting of fully protected double bond and allylic oxygen.

Research paper thumbnail of Studies towards lipid A: A synthetic strategy for the enantioselective preparation of 3-hydroxy fatty acids

Tetrahedron Asymmetry, Nov 1, 2006

A short and efficient enantioselective synthesis of (R)-3-hydroxydodecanoic acid is described, in... more A short and efficient enantioselective synthesis of (R)-3-hydroxydodecanoic acid is described, involving a Sharpless asymmetric dihydroxylation to produce the required (R)-stereochemistry.

Research paper thumbnail of A novel approach to the stereocontrolled synthesis of C-vinyl beta-D-galactopyranosides

Reaction of a lithiated dithiinyl reagent with a O-perbenzylated D-glycono-delta-lactone readily ... more Reaction of a lithiated dithiinyl reagent with a O-perbenzylated D-glycono-delta-lactone readily generates the corresponding masked C-vinyl galactosides in high yields and full beta-selectivity. Removal of the sulfur mask renders the free vinyl aglycone with the vinyl group in either the Z or E configuration, depending on the desulfurization conditions chosen.

Research paper thumbnail of A New Easy Conversion of Sulfoxides to Sulfides

Http Dx Doi Org 10 1080 03086648308073277, Dec 13, 2006

Research paper thumbnail of ChemInform Abstract: Highly Diastereoselective Preparation of anti‐α,β‐Dialkyl β‐Amino Acids Containing Natural α‐Amino Acid Side Chains

Research paper thumbnail of Asymmetric induction in the coupling of 5,6-dihydro-1,4-dithiins with chiral aldehydes. A new synthetic approach to polyhydroxylated compounds

Tetrahedron, 1996

A new strategy is designed to synthesize polyhydroxyl compounds (and/or carbohydrates) by couplin... more A new strategy is designed to synthesize polyhydroxyl compounds (and/or carbohydrates) by coupling of 5, 6-dihydro-1, 4-dithiins-carrying a vinylic hydrogen atom-with chiral aldehydes and, in sequence, stereoselective removal of the dithiodimethylene dithiin ...

Research paper thumbnail of A Stereoconvergent Tsuji–Trost Reaction in the Synthesis of Cyclohexenyl Nucleosides

Chemistry – A European Journal, 2020

(D.D.). Supporting information for this article is given via a link at the end of the document.

Research paper thumbnail of ChemInform Abstract: A One-Step Synthesis of 2,3-Dihydro-1,4-benzothiazines and Phenothiazines from 1,3-Thiazolidine Derivatives of Cyclohexanones

Research paper thumbnail of A view from space. Monitoring and management for World Heritage Sites

NASA and The Getty Conservation Institute are conducting an experiment in the application of remo... more NASA and The Getty Conservation Institute are conducting an experiment in the application of remotely sensed multispectral and radar data for monitoring change at World Heritage Sites. The project is concerned both with the principles of this approach and with current limitations. The latter have clearly demonstrated that automatic monitoring cannot be easily achieved, due to problems of low resolution, lack of repeatability, and cost, but the integration of this remotely sensed data with other data types into a geographic data management system may provide a monitoring management tool that can be used to test the potential of a fully integrated approach to site definition, monitoring, and management. The test case being adopted covers the area of Chaco Culture National Historic Park, in New Mexico, USA, a major Anasazi complex which is registered in the UNESCO’s World Heritage List. Data assembled included a variety of remotely-sensed information, GPS surveys, and the preparation o...

Research paper thumbnail of N-Butyl-L-Deoxynojirimycin (L-NBDNJ): Synthesis of an Allosteric Enhancer of α-Glucosidase Activity for the Treatment of Pompe Disease

Journal of medicinal chemistry, Jan 7, 2017

The highly stereocontrolled de novo synthesis of L-NBDNJ (the unnatural enantiomer of the iminosu... more The highly stereocontrolled de novo synthesis of L-NBDNJ (the unnatural enantiomer of the iminosugar drug Miglustat) and a preliminary evaluation of its chaperoning potential are herein reported. L-NBDNJ is able to enhance lysosomal α-glucosidase levels in Pompe disease fibroblasts, either when administered singularly or when co-incubated with the recombinant human α-glucosidase. In addition, differently from its D-enantiomer, L-NBDNJ does not act as a glycosidase inhibitor.

Research paper thumbnail of ChemInform Abstract: Asymmetric Synthesis of Optically Active Phthalides via ortho- Lithiation and Cyclization of Chiral N-Monosubstituted Benzamides

Research paper thumbnail of Synthesis of C-Protected 2,2-Dideutero � 3 -Amino Acids

Synthesis Stuttgart, 2006

Research paper thumbnail of Rapid access to 1,6-anhydro-beta-L-hexopyranose derivatives via domino reaction: Synthesis of L-allose and L-glucose

The Journal of Organic Chemistry, Aug 1, 2008

An expeditious and efficient synthesis of 1,6-anhydro-beta-L-hexopyranosyl derivatives 3 as valua... more An expeditious and efficient synthesis of 1,6-anhydro-beta-L-hexopyranosyl derivatives 3 as valuable building blocks for the preparation of L-sugars is herein reported. This route relies upon the use of a domino reaction involving five synthetic steps from the 5,6-dihydro-1,4-dithiin 4. As 1,6-anhydro derivatives 3 are obtained, dithioethylene bridge removal and double-bond dihydroxylation give access to protected L-allose and L-glucose in stereoselective fashion and high yields.

Research paper thumbnail of �-Amino-a-hydroxy Esters by Asymmetric Hydroxylation ofhomo-�-Amino Acid Esters

Research paper thumbnail of Reactivity of Ethanediyl S,S -Acetals; 2. Synthesis of 2,3-Dihydro-1,4-dithiins

Synthesis Stuttgart, 1991

Research paper thumbnail of Chemistry of Ethanediyl S,S-Acetals 9-Asymmetric Synthesis of Chiral cis Allylic Alcohols

Http Dx Doi Org 10 1080 00397919508011763, Sep 23, 2006

Research paper thumbnail of Synthesis of c-protected 2,2-dideutero β3-amino acids

Research paper thumbnail of Reactivity of Ethanediyl S,S-Acetals. Part 3. Ring Aromatization in Cyclohexanone Derivatives: A Novelty Synthesis of 1,4-Benzodithians

Research paper thumbnail of Mild Synthesis of Protected a-D-Glycosyl Iodides

Research paper thumbnail of ChemInform Abstract: Chemistry of Ethandiyl S,S-Acetals. Part 13. Aromatic Ring Bromination in 1,4-Benzothiazines, 1,4-Benzoxathianes and 1,4-Benzodithianes: The Occurrence of Vicarious Nucleophilic Substitution of Hydrogen and Electrophilic Aromatic Subs

Cheminform, 2010

ABSTRACT ChemInform is a weekly Abstracting Service, delivering concise information at a glance t... more ABSTRACT ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

Research paper thumbnail of A New Three Carbon Homologation Via Sulfur Containing Heterocyclic Systems

Phosphor Sulfur Silicon, 1999

A new reagent, based on a 5,6-dihydro-1,4-dithiin heterocyclic system, has been devised and conve... more A new reagent, based on a 5,6-dihydro-1,4-dithiin heterocyclic system, has been devised and conveniently used for 3 carbon elongations of various electrophiles. In fact, it acts as either a propenyl alcohol or an acrolein anion equivalent, introducing into the new molecule a moiety consisting of fully protected double bond and allylic oxygen.

Research paper thumbnail of Studies towards lipid A: A synthetic strategy for the enantioselective preparation of 3-hydroxy fatty acids

Tetrahedron Asymmetry, Nov 1, 2006

A short and efficient enantioselective synthesis of (R)-3-hydroxydodecanoic acid is described, in... more A short and efficient enantioselective synthesis of (R)-3-hydroxydodecanoic acid is described, involving a Sharpless asymmetric dihydroxylation to produce the required (R)-stereochemistry.

Research paper thumbnail of A novel approach to the stereocontrolled synthesis of C-vinyl beta-D-galactopyranosides

Reaction of a lithiated dithiinyl reagent with a O-perbenzylated D-glycono-delta-lactone readily ... more Reaction of a lithiated dithiinyl reagent with a O-perbenzylated D-glycono-delta-lactone readily generates the corresponding masked C-vinyl galactosides in high yields and full beta-selectivity. Removal of the sulfur mask renders the free vinyl aglycone with the vinyl group in either the Z or E configuration, depending on the desulfurization conditions chosen.

Research paper thumbnail of A New Easy Conversion of Sulfoxides to Sulfides

Http Dx Doi Org 10 1080 03086648308073277, Dec 13, 2006

Research paper thumbnail of ChemInform Abstract: Highly Diastereoselective Preparation of anti‐α,β‐Dialkyl β‐Amino Acids Containing Natural α‐Amino Acid Side Chains