Francisco J. Sayago

发表

Engineering strategy to improve peptide analogs: from structure-based computational design to tumor homing

Ruth Nussinov, Erkki Ruoslahti, Carlos Alemán, 2012, Journal of Computer-Aided Molecular Design.

Amide-triazole isosteric substitution for tuning self-assembly and incorporating new functions into soft supramolecular materials.

Francisco J. Sayago, Judith Mayr, C. Cativiela, 2015, Chemical communications.

Efficient access to enantiomerically pure cyclic alpha-amino esters through a lipase-catalyzed kinetic resolution.

Francisco J. Sayago, C. Cativiela, A. Jiménez, 2008, Tetrahedron, asymmetry.

Ring contraction of glycopyranosyl enamines: an easy route to furanoid thioglycosides of 5-aminosugars

Francisco J. Sayago, Consolación Gasch, J. Fuentes, 2004 .

Quantum-chemical predictions of redox potentials of carbamates in methanol.

Francisco J. Sayago, C. Cativiela, J. Urieta, 2011, Physical chemistry chemical physics : PCCP.

Nanoparticle-induced vascular blockade in human prostate cancer.

Ruth Nussinov, Michael J Sailor, Ji-Ho Park, 2010, Blood.

Lipase-catalyzed dynamic kinetic resolution of dimethyl (1,3-dihydro-2H-isoindol-1-yl)phosphonate

Francisco J. Sayago, C. Cativiela, V. Gotor‐Fernández, 2016 .

Stereodivergent Synthesis of Two Novel α-Aminophosphonic Acids Characterised by a cis-Fused Octahydroindole System

Francisco J. Sayago, C. Cativiela, A. Jiménez, 2011 .

Anhydroazasugars as key intermediates in the stereocontrolled preparation of azasugars and their ethyl thioglycosides

Francisco J. Sayago, Consolación Gasch, J. Fuentes, 2004 .

Synthesis of quaternary α-aminophosphonic acids

Francisco J. Sayago, C. Cativiela, M. Ordóñez, 2012 .

Stereoselective Synthesis of α-Amino-C-phosphinic Acids and Derivatives

Francisco J. Sayago, C. Cativiela, José Luis Viveros-Ceballos, 2016, Synthesis.

Remote Substituent Effects on the Stereoselectivity and Organocatalytic Activity of Densely Substituted Unnatural Proline Esters in Aldol Reactions

Francisco J. Sayago, C. Cativiela, A. Jiménez, 2015 .

First Synthesis of (R)‐ and (S)‐1,2,3,4‐Tetrahydroisoquinoline‐3‐phosphonic Acid (TicP) Using a Pictet–Spengler Reaction

Francisco J. Sayago, C. Cativiela, A. Jiménez, 2016 .

First Practical and Efficient Synthesis of 3‐Phosphorylated β‐Carboline Derivatives Using the Pictet–Spengler Reaction

Francisco J. Sayago, C. Cativiela, José Luis Viveros-Ceballos, 2015 .

Synthesis of [c]‐Fused Bicyclic Proline Analogues

Francisco J. Sayago, M. Calaza, C. Cativiela, 2015 .

d-Ribofuranosylenamine: a versatile starting material for preparing azasugar thioglycosides and building blocks for thioureylene-di-nucleosides

Francisco J. Sayago, Consolación Gasch, J. Fuentes, 2004 .

Synthesis of Phosphoproline Derivatives with an Octahydroisoindole Structure

Francisco J. Sayago, C. Cativiela, A. Jiménez, 2011 .

New approaches towards the synthesis of 1,2,3,4-tetrahydro isoquinoline-3-phosphonic acid (TicP)

Francisco J. Sayago, C. Cativiela, José Luis Viveros-Ceballos, 2021, Amino Acids.

First Synthesis of (R)- and (S)-1,2,3,4-Tetrahydroisoquinoline-3-phosphonic Acid (TicP) Using a Pictet-Spengler Reaction.

Francisco J. Sayago, C. Cativiela, A. Jiménez, 2016 .

Enzymatic and chromatographic resolution procedures applied to the synthesis of the phosphoproline enantiomers

Francisco J. Sayago, C. Cativiela, A. Jiménez, 2015 .

Practical access to the proline analogs (S,S,S)- and (R,R,R)-2-methyloctahydroindole-2-carboxylic acids by HPLC enantioseparation.

Francisco J. Sayago, M. Calaza, C. Cativiela, 2011, Chirality.

Efficient access to N-protected derivatives of (R,R,R)- and (S,S,S)-octahydroindole-2-carboxylic acid by HPLC resolution

Francisco J. Sayago, C. Cativiela, A. Jiménez, 2007 .

First Practical and Efficient Synthesis of 3‐Phosphorylated β‐Carboline Derivatives Using the Pictet—Spengler Reaction.

Francisco J. Sayago, C. Cativiela, José Luis Viveros-Ceballos, 2015 .

Efficient access to (1H)-isoindolin-1-one-3-carboxylic acid derivatives by orthopalladation and carbonylation of methyl arylglycinate substrates

Francisco J. Sayago, C. Cativiela, P. Laborda, 2011 .

An update on the stereoselective synthesis of α-aminophosphonic acids and derivatives

Francisco J. Sayago, C. Cativiela, José Luis Viveros-Ceballos, 2015 .

An Improved Synthesis of the Antibiotic Dehydrophos

Francisco J. Sayago, C. Cativiela, M. M. Jiménez‐Andreu, 2018, European Journal of Organic Chemistry.

Synthesis and biological activity of dehydrophos derivatives.

Francisco J. Sayago, C. Cativiela, J. Aínsa, 2019, Organic & biomolecular chemistry.

1-Aminovinylphosphonate Esters as Substrates for the Diels-Alder Reaction: First Synthetic and Theoretical Study

Francisco J. Sayago, C. Cativiela, P. Merino, 2019, European Journal of Organic Chemistry.

Stereocontrolled synthesis of iminocyclitols with an ether bridge

Francisco J. Sayago, Consolación Gasch, J. Fuentes, 2007 .

Stereoselective synthesis of azasugar thioglycosides

Francisco J. Sayago, Consolación Gasch, J. Fuentes, 2003 .

An easy route to seven-membered iminocyclitols from aldohexopyranosyl enamines

Francisco J. Sayago, Consolación Gasch, G. Repetto, 2002 .

Access to the cis-fused stereoisomers of proline analogues containing an octahydroindole core

Francisco J. Sayago, M. Calaza, C. Cativiela, 2011 .

Dynamic kinetic resolution of 1,3-dihydro-2H-isoindole-1-carboxylic acid methyl ester: asymmetric transformations toward isoindoline carbamates.

Francisco J. Sayago, C. Cativiela, V. Gotor‐Fernández, 2012, Organic letters.

A straightforward route to enantiopure alpha-substituted derivatives of (2S,3aS,7aS)-octahydroindole-2-carboxylic acid.

Francisco J. Sayago, M. Calaza, C. Cativiela, 2009, Tetrahedron.

Versatile methodology for the synthesis and α-functionalization of (2R,3aS,7aS)-octahydroindole-2-carboxylic acid.

Francisco J. Sayago, M. Calaza, C. Cativiela, 2008, Tetrahedron.

Cyclopalladation and reactivity of amino esters through C-H bond activation: experimental, kinetic, and density functional theory mechanistic studies.

Francisco J. Sayago, C. Cativiela, E. Laga, 2013, Chemistry.

Expeditious synthesis of sulfoazetidine spiro-C-glycosides from ketose acetals

Francisco J. Sayago, Consolación Gasch, J. Fuentes, 2006 .

Aldolase-catalyzed synthesis of conformationally constrained iminocyclitols: preparation of polyhydroxylated benzopyrrolizidines and cyclohexapyrrolizidines.

Francisco J. Sayago, C. Cativiela, J. Joglar, 2014, Organic letters.

Ru-catalyzed C-H functionalization of phenylglycine derivatives: Synthesis of isoquinoline-1-carboxylates and isoindoline-1-carboxylates

Francisco J. Sayago, C. Cativiela, E. Urriolabeitia, 2017 .

1-Aminovinylphosphonate Esters as Substrates for the Diels-Alder Reaction: First Synthetic and Theoretical Study

Francisco J. Sayago, C. Cativiela, P. Merino, 2019, European Journal of Organic Chemistry.

Towards the stereoselective synthesis of alpha-methylated (2S,3aS,7aS)-octahydroindole-2-carboxylic acid.

Francisco J. Sayago, M. Calaza, C. Cativiela, 2008, Tetrahedron, asymmetry.

Synthesis of β‐Aryl‐α,β‐Dehydroaminophosphonates by Pd‐Catalyzed Fujiwara–Moritani C−C Coupling

Francisco J. Sayago, E. Urriolabeitia, David Dalmau, 2024, European Journal of Organic Chemistry.