List of works - Yolanda Díaz

Advances in the enantioselective synthesis of carbocyclic nucleosides.

scientific article

An Efficient and General Enantioselective Synthesis of Sphingosine, Phythosphingosine, and 4-Substituted Derivatives†

scientific article published on 01 January 2009

Asymmetric sulfur ylide based enantioselective synthesis of D-erythro-sphingosine.

scientific article published on 17 October 2008

C1 and C2-symmetric carbohydrate phosphorus ligands in asymmetric catalysis

scientific article

C2-symmetric diphosphinite ligands derived from carbohydrates. The strong influence of remote stereocenters on asymmetric rhodium-catalyzed hydrogenation

scientific article published in October 2004

Chemical Access to d-Sarmentose Units Enables the Total Synthesis of Cardenolide Monoglycoside N-1 from Nerium oleander

scientific article

Conformationally-Locked N-Glycosides with Selective β-Glucosidase Inhibitory Activity: Identification of a New Non-Iminosugar-Type Pharmacological Chaperone for Gaucher Disease

scientific article published on 18 July 2012

Conformationally-locked N-glycosides: Exploiting long-range non-glycone interactions in the design of pharmacological chaperones for Gaucher disease

scientific article published on 04 November 2014

Designing an effective approach for obtaining methylenecarboxylate analogues of adenophostin A. Preliminary results

scientific article published in October 2009

Enantioselective Formal Synthesis of Nectrisine Using a Palladium-Catalyzed Asymmetric Allylic Amination and Cross-Metathesis as Key Steps

scientific article published on 02 June 2016

Enantioselective Synthesis of 3-Heterosubstituted-2-amino-1-ols by Sequential Metal-Free Diene Aziridination/Kinetic Resolution

scientific article published on 03 September 2019

Enantioselective Synthesis of Aminodiols by Sequential Rh-Catalysed Oxyamination/Kinetic Resolution. Expanding the Substrate Scope of Amidine-Based Catalysis

scientific article published on 17 January 2018

Fluorinated triazole-containing sphingosine analogues. Syntheses and in vitro evaluation as SPHK inhibitors

scientific article published on 01 October 2018

General Method for Synthesizing Pyranoid Glycals.A New Route to Allal and Gulal Derivatives

scientific article published on 01 February 2006

Highly efficient and stereoselective synthesis of beta-glycolipids

scientific article published on 11 December 2007

Mn(III) complexes with tridentate N,N,O-ligands as catalysts for the epoxidation of alkenes

Palladium-catalyzed allylic amination: a powerful tool for the enantioselective synthesis of acyclic nucleoside phosphonates

scientific article published on 01 August 2017

Recent Advances in the Synthesis of Sphingosine and Phytosphingosine, Molecules of Biological Significance

Recent advances in the glycosylation of sphingosines and ceramides.

scientific article published on 11 April 2007

Rhodium-catalyzed regio- and stereoselective oxyamination of dienes via tandem aziridination/ring-opening of dienyl carbamates

scientific article published on 01 July 2014

Ruthenium-catalyzed cross-metathesis with electron-rich phenyl vinyl sulfide enables access to 2,3-dideoxy-d-ribopyranose ring system donors

scholarly article in RSC Advances, vol. 4 no. 38, 2014

Selenium-controlled stereoselective synthesis of 2′-deoxynucleosides from glycals. A formal synthesis of AZT

Sequential Directed Epoxydation-Acidolysis from Glycals with MCPBA. A Flexible Approach to Protected Glycosyl Donors

Stannyl ceramides as efficient acceptors for synthesising β-galactosyl ceramides

scientific article published on 13 August 2008

Stereoselective synthesis of 2-deoxy-2-iodo-glycosides from furanoses. A new route to 2-deoxy-glycosides and 2-deoxy-oligosaccharides of ribo and xylo configuration.

scientific article published in December 2005

Stereoselective synthesis of both enantiomers of 1,4-anhydro-alditols, 1,4-anhydro-2-amino-alditols and d- and l-isonucleosides from 2,3-O-isopropylidene-d-glyceraldehyde using iodine-induced cyclization as the key step

Stereoselective synthesis of l-isonucleosides

Studies on the Zn(II)-mediated electrophilic selenocyclization and elimination of 3,4-O-isopropylidene-protected hydroxyalkenyl sulfides: synthesis of a 2-phenylselenenyl glycal

scientific article published on 04 March 2010

Syntheses of a Novel Fluorinated Trisphosphinoborate Ligand and Its Copper and Silver Complexes. Catalytic Activity toward Nitrene Transfer Reactions

scientific article published on 04 April 2014

Synthesis of 2-Iodoglycals, Glycals, and 1,1‘-Disaccharides from 2-Deoxy-2-iodopyranoses under Dehydrative Glycosylation Conditions

scientific article published on 11 October 2007

Synthesis of 2′-deoxy-2′-phenylselenenyl-furanosyl nucleosides from glycals using electrophilic selenium reagents. Conversion into 2′-deoxynucleosides

Synthesis of amino-1,4-anhydro-d-pentitols and amino-1,5-anhydro-d-hexitols with the arabino configuration from (R)-glycidol

Synthesis of carbohydrate-based vinyl selenides via Wittig-type reactions

scientific article published on 14 January 2007

Synthesis of erythro and threo furanoid glycals from 1- and 2-phenylselenenyl-carbohydrate derivatives.

scientific article published in November 2001

Synthesis ofd- andl-Carbocyclic Nucleosides via Rhodium-Catalyzed Asymmetric Hydroacylation as the Key Step

scientific article published on 25 September 2008

The reaction of pyranoside 2-uloses with DAST revised. Synthesis of 1-fluoro-ketofuranosyl fluorides and their reactivity with alcohols

Tuning the Stereoelectronic Properties of 1-Sulfanylhex-1-enitols for the Sequential Stereoselective Synthesis of 2-Deoxy-2-iodo-β-d-allopyranosides

scientific article published on 21 March 2014

List of works by Yolanda Díaz

Advances in the enantioselective synthesis of carbocyclic nucleosides.

An Efficient and General Enantioselective Synthesis of Sphingosine, Phythosphingosine, and 4-Substituted Derivatives†

Asymmetric sulfur ylide based enantioselective synthesis of D-erythro-sphingosine.

C1 and C2-symmetric carbohydrate phosphorus ligands in asymmetric catalysis

C2-symmetric diphosphinite ligands derived from carbohydrates. The strong influence of remote stereocenters on asymmetric rhodium-catalyzed hydrogenation

Chemical Access to d-Sarmentose Units Enables the Total Synthesis of Cardenolide Monoglycoside N-1 from Nerium oleander

Conformationally-Locked N-Glycosides with Selective β-Glucosidase Inhibitory Activity: Identification of a New Non-Iminosugar-Type Pharmacological Chaperone for Gaucher Disease

Conformationally-locked N-glycosides: Exploiting long-range non-glycone interactions in the design of pharmacological chaperones for Gaucher disease

Designing an effective approach for obtaining methylenecarboxylate analogues of adenophostin A. Preliminary results

Enantioselective Formal Synthesis of Nectrisine Using a Palladium-Catalyzed Asymmetric Allylic Amination and Cross-Metathesis as Key Steps

Enantioselective Synthesis of 3-Heterosubstituted-2-amino-1-ols by Sequential Metal-Free Diene Aziridination/Kinetic Resolution

Enantioselective Synthesis of Aminodiols by Sequential Rh-Catalysed Oxyamination/Kinetic Resolution. Expanding the Substrate Scope of Amidine-Based Catalysis

Fluorinated triazole-containing sphingosine analogues. Syntheses and in vitro evaluation as SPHK inhibitors

General Method for Synthesizing Pyranoid Glycals.A New Route to Allal and Gulal Derivatives

Highly efficient and stereoselective synthesis of beta-glycolipids

Mn(III) complexes with tridentate N,N,O-ligands as catalysts for the epoxidation of alkenes

Palladium-catalyzed allylic amination: a powerful tool for the enantioselective synthesis of acyclic nucleoside phosphonates

Recent Advances in the Synthesis of Sphingosine and Phytosphingosine, Molecules of Biological Significance

Recent advances in the glycosylation of sphingosines and ceramides.

Rhodium-catalyzed regio- and stereoselective oxyamination of dienes via tandem aziridination/ring-opening of dienyl carbamates

Ruthenium-catalyzed cross-metathesis with electron-rich phenyl vinyl sulfide enables access to 2,3-dideoxy-d-ribopyranose ring system donors

Selenium-controlled stereoselective synthesis of 2′-deoxynucleosides from glycals. A formal synthesis of AZT

Sequential Directed Epoxydation-Acidolysis from Glycals with MCPBA. A Flexible Approach to Protected Glycosyl Donors

Stannyl ceramides as efficient acceptors for synthesising β-galactosyl ceramides

Stereoselective synthesis of 2-deoxy-2-iodo-glycosides from furanoses. A new route to 2-deoxy-glycosides and 2-deoxy-oligosaccharides of ribo and xylo configuration.

Stereoselective synthesis of both enantiomers of 1,4-anhydro-alditols, 1,4-anhydro-2-amino-alditols and d- and l-isonucleosides from 2,3-O-isopropylidene-d-glyceraldehyde using iodine-induced cyclization as the key step

Stereoselective synthesis of l-isonucleosides

Studies on the Zn(II)-mediated electrophilic selenocyclization and elimination of 3,4-O-isopropylidene-protected hydroxyalkenyl sulfides: synthesis of a 2-phenylselenenyl glycal

Syntheses of a Novel Fluorinated Trisphosphinoborate Ligand and Its Copper and Silver Complexes. Catalytic Activity toward Nitrene Transfer Reactions

Synthesis of 2-Iodoglycals, Glycals, and 1,1‘-Disaccharides from 2-Deoxy-2-iodopyranoses under Dehydrative Glycosylation Conditions

Synthesis of 2′-deoxy-2′-phenylselenenyl-furanosyl nucleosides from glycals using electrophilic selenium reagents. Conversion into 2′-deoxynucleosides

Synthesis of amino-1,4-anhydro-d-pentitols and amino-1,5-anhydro-d-hexitols with the arabino configuration from (R)-glycidol

Synthesis of carbohydrate-based vinyl selenides via Wittig-type reactions

Synthesis of erythro and threo furanoid glycals from 1- and 2-phenylselenenyl-carbohydrate derivatives.

Synthesis ofd- andl-Carbocyclic Nucleosides via Rhodium-Catalyzed Asymmetric Hydroacylation as the Key Step

The reaction of pyranoside 2-uloses with DAST revised. Synthesis of 1-fluoro-ketofuranosyl fluorides and their reactivity with alcohols

Tuning the Stereoelectronic Properties of 1-Sulfanylhex-1-enitols for the Sequential Stereoselective Synthesis of 2-Deoxy-2-iodo-β-d-allopyranosides