Search Results - "Tulla‐Puche, Judit"

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  1. 1

    General Fmoc‐Based Solid‐Phase Synthesis of Complex Depsipeptides Circumventing Problematic Fmoc Removal by Lobo‐Ruiz, Ariadna, TullaPuche, Judit

    Published in European journal of organic chemistry (16-01-2020)
    “…Development of an Fmoc‐based solid‐phase depsipeptide methodology has been hampered by base‐promoted fragmentation and diketoperazine formation upon Fmoc group…”
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    Journal Article
  2. 2

    A Lasso‐Inspired Bicyclic Peptide: Synthesis, Structure and Properties by Martin‐Gómez, Helena, Albericio, Fernando, TullaPuche, Judit

    Published in Chemistry : a European journal (20-12-2018)
    “…The chemical synthesis of a bicycle inspired by the natural lasso peptide sungsanpin using a combination of solid‐phase and in‐solution chemistries is…”
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  3. 3

    2-Methoxy-4-methylsulfinylbenzyl: A Backbone Amide Safety-Catch Protecting Group for the Synthesis and Purification of Difficult Peptide Sequences by Paradís-Bas, Marta, Tulla-Puche, Judit, Albericio, Fernando

    Published in Chemistry : a European journal (10-11-2014)
    “…The use of 2‐methoxy‐4‐methylsulfinylbenzyl (Mmsb) as a new backbone amide‐protecting group that acts as a safety‐catch structure is proposed. Mmsb, which is…”
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  4. 4

    The road to the synthesis of "difficult peptides" by Paradís-Bas, Marta, Tulla-Puche, Judit, Albericio, Fernando

    Published in Chemical Society reviews (07-02-2016)
    “…The last decade has witnessed a renaissance of peptides as drugs. This progress, together with advances in the structural behavior of peptides, has attracted…”
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  5. 5

    ChemMatrix® for complex peptides and combinatorial chemistry by García-Ramos, Yésica, Paradís-Bas, Marta, Tulla-Puche, Judit, Albericio, Fernando

    Published in Journal of peptide science (01-12-2010)
    “…CM resin is a totally PEG‐based resin, made exclusively from primary ether bonds and therefore highly chemically stable. Compared to other PEG resins, it…”
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  6. 6

    Optimized Fmoc solid-phase synthesis of the cysteine-rich peptide linaclotide by Góngora-Benítez, Miriam, Tulla-Puche, Judit, Paradís-Bas, Marta, Werbitzky, Oleg, Giraud, Matthieu, Albericio, Fernando

    Published in Biopolymers (2011)
    “…Linaclotide, a small 14‐mer peptide highly rich in cysteines, is currently in phase III clinical trials for the treatment of gastrointestinal disorders. The…”
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  7. 7

    Polymers and drug delivery systems by Vilar, Gemma, Tulla-Puche, Judit, Albericio, Fernando

    Published in Current drug delivery (01-07-2012)
    “…In the treatment of health related dysfunctions, it is desirable that the drug reaches its site of action at a particular concentration and that this…”
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  8. 8

    Protection by Conformationally Restricted Mobility: First Solid-Phase Synthesis of Triostin A by Tulla-Puche, Judit, Marcucci, Eleonora, Fermin, Manuel, Bayó-Puxan, Núria, Albericio, Fernando

    Published in Chemistry : a European journal (19-05-2008)
    “…Conformationally restricted mobility: The application of an efficient solid‐phase strategy based on protection by conformationally restricted mobility (see…”
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  9. 9

    Total Solid-Phase Synthesis of the Azathiocoraline Class of Symmetric Bicyclic Peptides by Bayó-Puxan, Núria, Fernández, Ariadna, Tulla-Puche, Judit, Riego, Estela, Cuevas, Carmen, Álvarez, Mercedes, Albericio, Fernando

    Published in Chemistry : a European journal (04-12-2006)
    “…Thiocoraline is a potent antitumor agent isolated from the marine organism Micromonospora sp. This symmetric bicyclic depsipeptide binds the minor groove of…”
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    Journal Article
  10. 10

    "Head-to-side-chain" cyclodepsipeptides of marine origin by Pelay-Gimeno, Marta, Tulla-Puche, Judit, Albericio, Fernando

    Published in Marine Drugs (21-05-2013)
    “…Since the late 1980s, a large number of depsipeptides that contain a new topography, referred to as "head-to-side-chain" cyclodepsipeptides, have been isolated…”
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    Journal Article Book Review
  11. 11

    Investigation of the Biosynthesis of the Lasso Peptide Chaxapeptin Using an E. coli-Based Production System by Martin-Gómez, Helena, Linne, Uwe, Albericio, Fernando, Tulla-Puche, Judit, Hegemann, Julian D

    “…Lasso peptides are natural products belonging to the family of ribosomally synthesized and posttranslationally modified peptides (RiPPs) and are defined by…”
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  12. 12

    Solid-Phase Synthesis of NMe-IB-01212, a Highly N-Methylated Cyclic Peptide by Marcucci, Eleonora, Tulla-Puche, Judit, Albericio, Fernando

    Published in Organic letters (20-01-2012)
    “…N-Methylation of peptides is an important synthetic tool in peptide-based medicinal chemistry. Herein, an optimized strategy for solid-phase synthesis of small…”
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  13. 13

    Chemical Modification of Microcin J25 Reveals New Insights on the Stereospecific Requirements for Antimicrobial Activity by Martin-Gómez, Helena, Jorba, Marta, Albericio, Fernando, Viñas, Miguel, Tulla-Puche, Judit

    “…In this study, microcin J25, a potent antimicrobial lasso peptide that acts on Gram-negative bacteria, was subjected to a harsh treatment with a base in order…”
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  14. 14

    Eco-Friendly Combination of the Immobilized PGA Enzyme and the S-Phacm Protecting Group for the Synthesis of Cys-Containing Peptides by Góngora-Benítez, Miriam, Basso, Alessandra, Bruckdorfer, Thomas, Royo, Miriam, Tulla-Puche, Judit, Albericio, Fernando

    Published in Chemistry : a European journal (07-12-2012)
    “…Enzyme‐labile protecting groups have emerged as a green alternative to conventional protecting groups. These groups introduce a further orthogonal dimension…”
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  15. 15

    The first total synthesis of the cyclodepsipeptide pipecolidepsin A by Pelay-Gimeno, Marta, García-Ramos, Yésica, Jesús Martin, Maria, Spengler, Jan, Molina-Guijarro, José Manuel, Munt, Simon, Francesch, Andrés M., Cuevas, Carmen, Tulla-Puche, Judit, Albericio, Fernando

    Published in Nature communications (30-08-2013)
    “…Pipecolidepsin A is a head-to-side-chain cyclodepsipeptide isolated from the marine sponge Homophymia lamellosa . This compound shows relevant cytotoxic…”
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    Acid-Labile Cys-Protecting Groups for the Fmoc/tBu Strategy: Filling the Gap by Góngora-Benítez, Miriam, Mendive-Tapia, Lorena, Ramos-Tomillero, Iván, Breman, Arjen C, Tulla-Puche, Judit, Albericio, Fernando

    Published in Organic letters (02-11-2012)
    “…To address the existing gap in the current set of acid-labile Cys-protecting groups for the Fmoc/tBu strategy, diverse Fmoc-Cys(PG)-OH derivatives were…”
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    Journal Article
  19. 19

    RADA-16: A Tough Peptide - Strategies for Synthesis and Purification by Paradís-Bas, Marta, Tulla-Puche, Judit, Zompra, Aikaterini A., Albericio, Fernando

    Published in European journal of organic chemistry (01-09-2013)
    “…The self‐assembling capacity of certain molecules can be exploited for a diverse range of biomedical applications. The ionic complementary peptide RADA‐16 is…”
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  20. 20

    Enzyme-Labile Protecting Groups for the Synthesis of Natural Products: Solid-Phase Synthesis of Thiocoraline by Tulla-Puche, Judit, Góngora-Benítez, Miriam, Bayó-Puxan, Núria, Francesch, Andrés M., Cuevas, Carmen, Albericio, Fernando

    Published in Angewandte Chemie International Edition (27-05-2013)
    “…Another (orthogonal) dimension: The solid‐phase synthesis of thiocoraline was accomplished for the first time by a combined approach involving chemical and…”
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