Y. Díaz

发表

Conformationally-locked N-glycosides with selective β-glucosidase inhibitory activity: identification of a new non-iminosugar-type pharmacological chaperone for Gaucher disease.

Yoshiyuki Suzuki, K. Higaki, E. Nanba, 2012, Journal of medicinal chemistry.

Synthesis of Hyperbranched β‐Galceramide‐Containing Dendritic Polymers that Bind HIV‐1 rgp120

O. Boutureira, S. Castillón, À. Serra, 2010 .

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

S. Castillón, Y. Díaz, F. Bravo, 2001 .

Stereoselective Tandem Epoxidation–Alcoholysis/Hydrolysis of Glycals with Molybdenum Catalysts

S. Castillón, Y. Díaz, M. Matheu, 2010 .

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

Yoshiyuki Suzuki, K. Higaki, E. Nanba, 2015, European journal of medicinal chemistry.

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

Joan Guasch, F. Maseras, S. Castillón, 2018, Chemistry.

Synthesis of C‐Nucleosides

S. Castillón, Y. Díaz, M. Matheu, 2013 .

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

S. Castillón, Y. Díaz, M. Matheu, 2017, The Journal of organic chemistry.

General method for synthesizing pyranoid glycals. A new route to allal and gulal derivatives.

Miguel A. Rodríguez, S. Castillón, Y. Díaz, 2006, Organic letters.

Revealing 2-dimethylhydrazino-2-alkyl alkynyl sphingosine derivatives as sphingosine kinase 2 inhibitors: Some hints on the structural basis for selective inhibition.

X. Barril, R. Beltrán-Debón, M. Sanz, 2022, Bioorganic chemistry.

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

S. Castillón, Y. Díaz, M. Matheu, 2014 .

1,2‐Addition of Nucleophiles to Carbonyl Compounds

S. Castillón, Y. Díaz, M. Matheu, 2013 .

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

S. Castillón, A. Morère, Y. Díaz, 2009, Carbohydrate research.

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

R. Beltrán-Debón, S. Castillón, Y. Díaz, 2018, Organic & biomolecular chemistry.

Synthesis of 2-iodoglycals, glycals, and 1,1'-disaccharides from 2-Deoxy-2-iodopyranoses under dehydrative glycosylation conditions.

P. Seeberger, Miguel A. Rodríguez, S. Castillón, 2007, The Journal of organic chemistry.

Tuning the stereoelectronic properties of 1-sulfanylhex-1-enitols for the sequential stereoselective synthesis of 2-deoxy-2-iodo-β-D-allopyranosides.

A. Kövér, S. Castillón, Y. Díaz, 2014, The Journal of organic chemistry.

1,4‐Addition of Nucleophiles to α,β‐Unsaturated Carbonyl Compounds

S. Castillón, Y. Díaz, M. Matheu, 2013 .

Synthesis of a P‐Stereogenic PNPtBu,Ph Ruthenium Pincer Complex and Its Application in Asymmetric Reduction of Ketones

S. Castillón, Y. Díaz, M. Matheu, 2015 .

Stereoselective Glycosylations of a Family of 6-Deoxy-1,2-glycals Generated by Catalytic Alkynol Cycloisomerization

F. McDonald, Y. Díaz, and K. Subba Reddy, 2000 .

Highly reactive 2-deoxy-2-iodo-d-allo and d-gulo pyranosyl sulfoxide donors ensure β-stereoselective glycosylations with steroidal aglycones

Miguel A. Rodríguez, S. Castillón, David Benito-Alifonso, 2018, RSC advances.

Stereoselective synthesis of 2-deoxy-2-phenylselenenyl glycosides from furanoses : Implication of the phenylselenenyl group in the stereocontrolled preparation of 2-deoxy-ribo-and 2 -deoxy -xylo -oligosaccharides

Miguel A. Rodríguez, S. Castillón, Y. Díaz, 2007 .

Stereoselective synthesis of 2-deoxyglycosides from sulfanyl alkenes by consecutive one pot cyclization and glycosylation reactions

Miguel A. Rodríguez, S. Castillón, Y. Díaz, 2007 .

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

S. Castillón, Y. Díaz, F. Bravo, 2001, Carbohydrate research.

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.

Miguel A. Rodríguez, S. Castillón, Y. Díaz, 2005, The Journal of organic chemistry.

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

G. Jana, M. Jimeno, S. Castillón, 2001 .

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

S. Castillón, Y. Díaz, A. El‐Laghdach, 1997 .

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

S. Castillón, Y. Díaz, M. Matheu, 2007, Carbohydrate research.

Advances in the enantioselective synthesis of carbocyclic nucleosides.

S. Castillón, Y. Díaz, M. Matheu, 2013, Chemical Society reviews.

C1 and C2-symmetric carbohydrate phosphorus ligands in asymmetric catalysis.

C. Claver, S. Castillón, Y. Díaz, 2005, Chemical Society reviews.

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

C. Claver, A. Masdeu-Bultó, S. Castillón, 2004, The Journal of organic chemistry.

Sequential directed epoxydation-acidolysis from glycals with MCPBA. A flexible approach to protected glycosyl donors.

S. Castillón, J. Castilla, Y. Díaz, 2011, The Journal of organic chemistry.

Synthesis of Purine and Pyrimidine Isodideoxynucleosides from (S)-Glycydol Using Iodoetherification as Key Step. Synthesis of (S,S)-iso-ddA1

S. Castillón, Y. Díaz, F. Bravo, 1999 .

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

Joan Guasch, F. Maseras, S. Castillón, 2019, Chemistry.

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

Joan Guasch, S. Castillón, Y. Díaz, 2014, Chemical communications.

Synthesis of D- and L-carbocyclic nucleosides via rhodium-catalyzed asymmetric hydroacylation as the key step.

S. Castillón, Y. Díaz, M. Matheu, 2008, Organic letters.

Carbohydrate derivative ligands in asymmetric catalysis

C. Claver, O. Pàmies, M. Diéguez, 2004 .

Syntheses of a novel fluorinated trisphosphinoborate ligand and its copper and silver complexes. Catalytic activity toward nitrene transfer reactions.

E. Álvarez, P. Pérez, A. Caballero, 2014, Inorganic chemistry.

Substrate-Regiocontrolled Synthesis of Enantioenriched Allylic Amines by Palladium-Catalysed Asymmetric Allylic Amination: Formal Synthesis of Fagomine

S. Castillón, Y. Díaz, M. Escudero-Casao, 2016 .

New C2‐ and C1‐Symmetric Phosphorus Ligands Based on Carbohydrate Scaffolds and Their Use in the Iridium‐Catalysed Hydrogenation of Ketimines

C. Claver, S. Castillón, Y. Díaz, 2006 .

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

S. Castillón, Y. Díaz, M. Matheu, 2016, The Journal of organic chemistry.

Highly efficient and stereoselective synthesis of beta-glycolipids.

S. Castillón, J. A. Morales-Serna, Y. Díaz, 2008, Organic & biomolecular chemistry.

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

Miguel A. Rodríguez, S. Castillón, Y. Díaz, 2010, Carbohydrate research.

Recent advances in the glycosylation of sphingosines and ceramides.

S. Castillón, J. A. Morales-Serna, Y. Díaz, 2007, Carbohydrate research.

Direct and Efficient Glycosylation Protocol for Synthesizing α‐Glycolipids: Application to the Synthesis of KRN7000

S. Castillón, J. A. Morales-Serna, Y. Díaz, 2008 .

Efficient Synthesis of β‐Glycosphingolipids by Reaction of Stannylceramides with Glycosyl Iodides Promoted by TBAI/AW 300 Molecular Sieves

S. Castillón, J. A. Morales-Serna, Y. Díaz, 2009 .

Stannyl ceramides as efficient acceptors for synthesising beta-galactosyl ceramides.

S. Castillón, J. A. Morales-Serna, Y. Díaz, 2008, Organic & biomolecular chemistry.

Enantioselective Synthesis of Jaspine B (Pachastrissamine) and Its C-2 and/or C-3 Epimers†

S. Castillón, Y. Díaz, M. Matheu, 2011 .

Metal-free and VOC-free O-glycosylation in supercritical CO2

S. Castillón, Y. Díaz, M. Matheu, 2017 .

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

S. Castillón, Y. Díaz, M. Escudero-Casao, 2017, Organic & biomolecular chemistry.

Towards the preparation of 2″-deoxy-2″-fluoro-adenophostin A. Study of the glycosylation reaction

S. Castillón, A. Morère, Y. Díaz, 2008 .

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

S. Castillón, J. A. Morales-Serna, Y. Díaz, 2010 .

An efficient and general enantioselective synthesis of sphingosine, phythosphingosine, and 4-substituted derivatives.

S. Castillón, Y. Díaz, M. Matheu, 2009, Organic letters.

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

S. Castillón, J. A. Morales-Serna, Y. Díaz, 2008, Organic & biomolecular chemistry.

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

S. Castillón, Y. Díaz, F. Bravo, 2003 .

Stereoselective synthesis of l-isonucleosides

S. Castillón, Y. Díaz, F. Bravo, 2003 .

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

S. Castillón, Y. Díaz, A. El‐Laghdach, 1993 .

Stereoselective Synthesis of 2‘,3‘-Dideoxynucleosides by Addition of Selenium Electrophiles to Glycals. A Formal Synthesis of D4T from 2-Deoxyribose

S. Castillón, Y. Díaz, A. El‐Laghdach, 1997 .

Selenium-Controlled Stereoselective Synthesis of 2′-Deoxynucleosides from Glycals. A Formal Synthesis of AZT.

S. Castillón, Y. Díaz, A. El‐Laghdach, 1993 .

Stereoselective Synthesis of L-Isonucleosides.

S. Castillón, Y. Díaz, F. Bravo, 2003 .

Short and general procedure for synthesizing cis-1,2-fused 1,3-oxathiolan-, 1,3-oxaselenolan-, and 1,3-oxazolidin-2-imine carbohydrate derivatives.

S. Castillón, J. Castilla, Y. Díaz, 2010, The Journal of organic chemistry.

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.

S. Castillón, Y. Díaz, F. Bravo, 2001 .

Stereoselective Synthesis of Homochiral Substituted Tetrahydrothiophenes by Electrophile‐Promoted Thioetherification

G. Jana, S. Castillón, Y. Díaz, 2003 .

Stereoselective Synthesis of Homochiral Substituted Tetrahydrothiophenes by Electrophile‐Promoted Thioetherification.

G. Jana, S. Castillón, Y. Díaz, 2003 .

Interactive comment on “Formation of secondary organic aerosols from the ozonolysis of dihydrofurans” by

Y. Díaz, 2016 .

Conformationally-locked N-glycosides with selective β-glucosidase inhibitory activity: identification of a new non-iminosugar-type pharmacological chaperone for Gaucher disease.

Yoshiyuki Suzuki, K. Higaki, E. Nanba, 2012, Journal of medicinal chemistry.