Judit Tulla-Puche

发表

Multifaceted roles of disulfide bonds. Peptides as therapeutics.

Miriam Góngora-Benítez, Judit Tulla-Puche, F. Albericio, 2014, Chemical reviews.

RADA‐16: A Tough Peptide – Strategies for Synthesis and Purification

Judit Tulla-Puche, F. Albericio, Aikaterini A Zompra, 2013 .

Fmoc Methodology: Cleavage from the Resin and Final Deprotection

Judit Tulla-Puche, F. Albericio, S. Kates, 2011 .

The synergy of ChemMatrix resin and pseudoproline building blocks renders RANTES, a complex aggregated chemokine.

Judit Tulla-Puche, F. Albericio, P. White, 2006, Biopolymers.

The (Classic Concept of) Solid Support

Judit Tulla-Puche, F. Albericio, 2009 .

Thioester Bonds of Thiocoraline Can Be Replaced with NMe-Amide Bridges without Affecting Its DNA-Binding Properties.

Judit Tulla-Puche, F. Albericio, K. Fox, 2014, ACS medicinal chemistry letters.

Total solid-phase synthesis of the azathiocoraline class of symmetric bicyclic peptides.

Fernando Albericio, Mercedes Alvarez, Carmen Cuevas, 2006, Chemistry.

Enzyme-labile protecting groups for the synthesis of natural products: solid-phase synthesis of thiocoraline.

Miriam Góngora-Benítez, Judit Tulla-Puche, F. Albericio, 2013, Angewandte Chemie.

Orthogonal chemistry for the synthesis of thiocoraline-triostin hybrids. Exploring their structure-activity relationship.

Judit Tulla-Puche, F. Albericio, C. Falciani, 2013, Journal of medicinal chemistry.

Oxathiocoraline: Lessons to be Learned from the Synthesis of Complex N‐Methylated Depsipeptides

Judit Tulla-Puche, F. Albericio, N. Bayó-Puxan, 2009 .

Solid-phase synthesis of NMe-IB-01212, a highly N-methylated cyclic peptide.

Judit Tulla-Puche, F. Albericio, E. Marcucci, 2012, Organic letters.

Solid-phase syntheses of furopyridine and furoquinoline systems.

Pablo Cironi, Judit Tulla-Puche, F. Albericio, 2004, Organic letters.

Synthetic Circularized Analogues of Bovine Pancreatic Trypsin Inhibitor

Judit Tulla-Puche, F. Albericio, G. Bárány, 2004 .

Rescuing biological activity from synthetic phakellistatin 19.

Judit Tulla-Puche, F. Albericio, Marta Pelay-Gimeno, 2013, Journal of medicinal chemistry.

Synthesis of complex head-to-side-chain cyclodepsipeptides

Judit Tulla-Puche, F. Albericio, Marta Pelay-Gimeno, 2016, Nature Protocols.

Stellatolides, a new cyclodepsipeptide family from the sponge Ecionemia acervus: isolation, solid-phase total synthesis, and full structural assignment of stellatolide A.

Judit Tulla-Puche, F. Albericio, F. Reyes, 2014, Journal of the American Chemical Society.

General Fmoc-Based Solid-Phase Synthesis of Complex Depsipeptides Circumventing Problematic Fmoc Removal

Judit Tulla-Puche, A. Lobo-Ruiz, 2019 .

Understanding Acid Lability of Cysteine Protecting Groups

Miriam Góngora-Benítez, Judit Tulla-Puche, F. Albericio, 2013, Molecules.

Lasso peptides: chemical approaches and structural elucidation.

Judit Tulla-Puche, Helena Martin‐Gómez, Helena Martin-Gómez, 2018, Organic & biomolecular chemistry.

Solid-Phase Synthesis of Aza-Kahalalide F Analogues: (2R,3R)-2-Amino-3-azidobutanoic Acid as Precursor of the Aza-Threonine

Judit Tulla-Puche, F. Albericio, C. Cuevas, 2010 .

2-Methoxy-4-methylsulfinylbenzyl: a backbone amide safety-catch protecting group for the synthesis and purification of difficult peptide sequences.

Judit Tulla-Puche, F. Albericio, Marta Paradís-Bas, 2014, Chemistry.

Chemical Modification of Microcin J25 Reveals New Insights on the Stereospecific Requirements for Antimicrobial Activity

Judit Tulla-Puche, F. Albericio, M. Viñas, 2019, International journal of molecular sciences.

Optimized Fmoc solid‐phase synthesis of Thymosin α1 by side‐chain anchoring onto a PEG resin

Judit Tulla-Puche, F. Albericio, M. Giraud, 2009, Biopolymers.

Investigation of the Biosynthesis of the Lasso Peptide Chaxapeptin Using an E. coli-Based Production System.

U. Linne, Judit Tulla-Puche, F. Albericio, 2018, Journal of natural products.

Chemical Synthesis of 19F-labeled HIV-1 Protease using Fmoc-Chemistry and ChemMatrix Resin

E. Giralt, Judit Tulla-Puche, F. Albericio, 2007, International Journal of Peptide Research and Therapeutics.

Stellatolides, a New Cyclodepsipeptide Family from the Sponge Ecionemia acervus: Isolation, Solid‐Phase Total Synthesis, and Full Structural Assignment of Stellatolide A.

Judit Tulla-Puche, 2014 .

“Head-to-Side-Chain” Cyclodepsipeptides of Marine Origin

Fernando Albericio, Judit Tulla-Puche, F. Albericio, 2013, Marine drugs.

Methods for the Peptide Synthesis and Analysis

Judit Tulla-Puche, F. Albericio, A. El‐Faham, 2015 .

Protection by conformationally restricted mobility: first solid-phase synthesis of triostin A.

Judit Tulla-Puche, F. Albericio, N. Bayó-Puxan, 2008, Chemistry.

The synthesis of naturally occurring peptides and their analogs.

Judit Tulla-Puche, F. Albericio, J. Spengler, 2007, Current opinion in drug discovery & development.

N,N,N',N'-tetramethylchloroformamidinium hexafluorophosphate (TCFH), a powerful coupling reagent for bioconjugation.

Judit Tulla-Puche, F. Albericio, M. Royo, 2008, Bioconjugate chemistry.

On-resin native chemical ligation for cyclic peptide synthesis.

Judit Tulla-Puche, G. Bárány, G. Barany, 2004, The Journal of organic chemistry.

Synthetic approaches of naturally and rationally designed peptides and peptidomimetics

Judit Tulla-Puche, A. Lobo-Ruiz, 2018 .

Handles for Fmoc solid-phase synthesis of protected peptides.

Miriam Góngora-Benítez, Judit Tulla-Puche, F. Albericio, 2013, ACS combinatorial science.

Synthetic Approaches to Disulfide-free Circular Bovine Pancreatic Trypsin Inhibitor (c-BPTI) Analogues

C. Woodward, Judit Tulla-Puche, F. Albericio, 2006, International Journal of Peptide Research and Therapeutics.

Constella™(EU)-Linzess™(USA): the last milestone in the long journey of the peptide linaclotide and its implications for the future of peptide drugs.

Miriam Góngora-Benítez, Judit Tulla-Puche, F. Albericio, 2013, Future medicinal chemistry.

Synthesis of cyclohexapeptides as antimalarial and anti-trypanosomal agents

V. Yardley, Judit Tulla-Puche, F. Albericio, 2014 .

The first total synthesis of the cyclodepsipeptide pipecolidepsin A

Judit Tulla-Puche, F. Albericio, C. Cuevas, 2013, Nature Communications.

Fmoc Methodology: Cleavage from the Resin and Final Deprotection

Judit Tulla-Puche, F. Albericio, S. Kates, 2011 .

Single-molecule kinetics and footprinting of DNA bis-intercalation: the paradigmatic case of Thiocoraline

F. Ritort, Judit Tulla-Puche, F. Albericio, 2015, Nucleic acids research.

Development of resin-to-resin transfer reactions (RRTR) using Sonogashira chemistry

Judit Tulla-Puche, Judit Tulla-Puche, George Barany, 2005 .

ChemMatrix, a poly(ethylene glycol)-based support for the solid-phase synthesis of complex peptides.

Judit Tulla-Puche, F. Albericio, F. García-Martín, 2006, Journal of combinatorial chemistry.

Eco-friendly combination of the immobilized PGA enzyme and the S-Phacm protecting group for the synthesis of Cys-containing peptides.

Miriam Góngora-Benítez, Judit Tulla-Puche, F. Albericio, 2012, Chemistry.

Cysteine-S-trityl a key derivative to prepare N-methyl cysteines.

Judit Tulla-Puche, F. Albericio, N. Bayó-Puxan, 2008, Journal of combinatorial chemistry.

Polymers and drug delivery systems.

Judit Tulla-Puche, F. Albericio, G. Vilar, 2012, Current drug delivery.

The Road to the Synthesis of “Difficult Peptides”

Judit Tulla-Puche, F. Albericio, Marta Paradís-Bas, 2016 .

The road to the synthesis of "difficult peptides".

Judit Tulla-Puche, F. Albericio, Marta Paradís-Bas, 2016, Chemical Society reviews.

Partially folded bovine pancreatic trypsin inhibitor analogues attain fully native structures when co-crystallized with S195A rat trypsin.

C. Woodward, D. Ohlendorf, Judit Tulla-Puche, 2008, Journal of molecular biology.

ChemMatrix® for complex peptides and combinatorial chemistry

Judit Tulla-Puche, F. Albericio, Marta Paradís-Bas, 2010, Journal of peptide science : an official publication of the European Peptide Society.

From the one-bead-one-compound concept to one-bead-one-reactor.

Judit Tulla-Puche, F. Albericio, O. Cascone, 2007, Journal of combinatorial chemistry.

Synthesis of orthogonally protected l-threo-β-ethoxyasparagine

Judit Tulla-Puche, F. Albericio, J. Spengler, 2010, Amino Acids.

A new quinoxaline-containing peptide induces apoptosis in cancer cells by autophagy modulation

Judit Tulla-Puche, F. Albericio, A. Zorzano, 2015, Chemical science.

Resin-to-Resin Transfer Reactions (RRTR) via Sonogashira Coupling

Judit Tulla-Puche, F. Albericio, R. Majerle, 2012 .

Semipermanent C-terminal carboxylic acid protecting group: application to solubilizing peptides and fragment condensation.

Judit Tulla-Puche, F. Albericio, Marta Paradís-Bas, 2015, Organic Letters.

Acid-labile Cys-protecting groups for the Fmoc/tBu strategy: filling the gap.

Miriam Góngora-Benítez, Judit Tulla-Puche, F. Albericio, 2012, Organic letters.

The power of functional resins in organic synthesis

Judit Tulla-Puche, F. Albericio, 2008 .

A universal strategy for preparing protected C-terminal peptides on the solid phase through an intramolecular click chemistry-based handle.

Miriam Góngora-Benítez, Judit Tulla-Puche, F. Albericio, 2012, Chemical communications.

Optimized Fmoc solid‐phase synthesis of the cysteine‐rich peptide linaclotide

Miriam Góngora-Benítez, Judit Tulla-Puche, F. Albericio, 2011, Biopolymers.

Linear versus branched poly-lysine/arginine as polarity enhancer tags

Judit Tulla-Puche, F. Albericio, Marta Paradís-Bas, 2014 .