Works by Gois, Pedro M. P.
Results: 42
Cover Feature: Engineering the BASHY Dye Platform toward Architectures with Responsive Fluorescence (Chem. Eur. J. 31/2023).
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- Chemistry - A European Journal, 2023, v. 29, n. 31, p. 1, doi. 10.1002/chem.202301399
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- Article
Engineering the BASHY Dye Platform toward Architectures with Responsive Fluorescence.
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- Chemistry - A European Journal, 2023, v. 29, n. 31, p. 1, doi. 10.1002/chem.202300579
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- Article
Front Cover: Interactive Bioconjugation at N‐Terminal Cysteines by Using O‐Salicylaldehyde Esters towards Dual Site‐Selective Functionalization (Chem. Eur. J. 67/2022).
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- Chemistry - A European Journal, 2022, v. 28, n. 67, p. 1, doi. 10.1002/chem.202203566
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- Article
Interactive Bioconjugation at N‐Terminal Cysteines by Using O‐Salicylaldehyde Esters towards Dual Site‐Selective Functionalization.
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- Chemistry - A European Journal, 2022, v. 28, n. 67, p. 1, doi. 10.1002/chem.202202377
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- Article
Cysteine‐Assisted Click‐Chemistry for Proximity‐Driven, Site‐Specific Acetylation of Histones.
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- Angewandte Chemie, 2022, v. 134, n. 46, p. 1, doi. 10.1002/ange.202208543
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Diazaborines Are a Versatile Platform to Develop ROS‐Responsive Antibody Drug Conjugates**.
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- Angewandte Chemie, 2021, v. 133, n. 49, p. 26118, doi. 10.1002/ange.202109835
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Efficient Amino‐Sulfhydryl Stapling on Peptides and Proteins Using Bifunctional NHS‐Activated Acrylamides.
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- Angewandte Chemie, 2021, v. 133, n. 19, p. 10945, doi. 10.1002/ange.202016936
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Modulation of Human Phenylalanine Hydroxylase by 3-Hydroxyquinolin-2(1H)-One Derivatives.
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- Biomolecules (2218-273X), 2021, v. 11, n. 3, p. 462, doi. 10.3390/biom11030462
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Towards Selective Delivery of a Ruthenium(II) Polypyridyl Complex‐Containing Bombesin Conjugate into Cancer Cells.
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- ChemBioChem, 2023, v. 24, n. 4, p. 1, doi. 10.1002/cbic.202200647
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Unveiling the Potential of Transition Metal Complexes for Medicine: Translational in Situ Activation of Metal‐Based Drugs from Bench to in Vivo Applications.
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- ChemBioChem, 2021, v. 22, n. 10, p. 1740, doi. 10.1002/cbic.202100015
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Glycerol as an Efficient Medium for the Petasis Borono-Mannich Reaction.
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- ChemistryOpen, 2015, v. 4, n. 1, p. 39, doi. 10.1002/open.201402066
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Tuning the Reactivity of Dirhodium(II) Complexes with Axial N-Heterocyclic Carbene Ligands: The Arylation of Aldehydes.
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- Angewandte Chemie International Edition, 2007, v. 46, n. 30, p. 5750, doi. 10.1002/anie.200700924
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- Article
BASHY Dye Platform Enables the Fluorescence Bioimaging of Myelin Debris Phagocytosis by Microglia during Demyelination.
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- Cells (2073-4409), 2021, v. 10, n. 11, p. 3163, doi. 10.3390/cells10113163
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- Article
Hypervalent Iodine Mediated Sulfonamide Synthesis.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 15, p. 2695, doi. 10.1002/ejoc.201900259
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Cysteine‐Assisted Click‐Chemistry for Proximity‐Driven, Site‐Specific Acetylation of Histones.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 46, p. 1, doi. 10.1002/anie.202208543
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- Article
Diazaborines Are a Versatile Platform to Develop ROS‐Responsive Antibody Drug Conjugates**.
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- Angewandte Chemie International Edition, 2021, v. 60, n. 49, p. 25914, doi. 10.1002/anie.202109835
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- Article
Efficient Amino‐Sulfhydryl Stapling on Peptides and Proteins Using Bifunctional NHS‐Activated Acrylamides.
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- Angewandte Chemie International Edition, 2021, v. 60, n. 19, p. 10850, doi. 10.1002/anie.202016936
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- Article
The Role of Electron Transfer in the Fragmentation of Phenyl and Cyclohexyl Boronic Acids.
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- International Journal of Molecular Sciences, 2019, v. 20, n. 22, p. 5578, doi. 10.3390/ijms20225578
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Rhodium-Catalysed Tandem Hydroformylation/Arylation Reaction with Boronic Acids.
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- Advanced Synthesis & Catalysis, 2014, v. 356, n. 6, p. 1223, doi. 10.1002/adsc.201300968
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Asymmetric Intramolecular CH Insertion of α-Diazoacetamides in Water by Dirhodium(II) Catalysts Derived from Natural Amino Acids.
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- Advanced Synthesis & Catalysis, 2012, v. 354, n. 16, p. 2921, doi. 10.1002/adsc.201200101
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Polyoxazoline‐Based Nanovaccine Synergizes with Tumor‐Associated Macrophage Targeting and Anti‐PD‐1 Immunotherapy against Solid Tumors.
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- Advanced Science, 2023, v. 10, n. 25, p. 1, doi. 10.1002/advs.202300299
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Engineering Boron Hot Spots for the Site‐Selective Installation of Iminoboronates on Peptide Chains.
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- Chemistry - A European Journal, 2020, v. 26, n. 66, p. 15226, doi. 10.1002/chem.202002675
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- Article
Cover Feature: Cyanine‐Like Boronic Acid‐Derived Salicylidenehydrazone Complexes (Cy‐BASHY) for Bioimaging Applications (Chem. Eur. J. 62/2020).
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- Chemistry - A European Journal, 2020, v. 26, n. 62, p. 14022, doi. 10.1002/chem.202003340
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Cyanine‐Like Boronic Acid‐Derived Salicylidenehydrazone Complexes (Cy‐BASHY) for Bioimaging Applications.
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- Chemistry - A European Journal, 2020, v. 26, n. 62, p. 14064, doi. 10.1002/chem.202001623
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Bioconjugation with Maleimides: A Useful Tool for Chemical Biology.
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- Chemistry - A European Journal, 2019, v. 25, n. 1, p. 43, doi. 10.1002/chem.201803174
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N,O‐Iminoboronates: Reversible Iminoboronates with Improved Stability for Cancer Cells Targeted Delivery.
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- Chemistry - A European Journal, 2018, v. 24, n. 48, p. 12495, doi. 10.1002/chem.201802515
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Highly Efficient Energy Transfer Cassettes by Assembly of Boronic Acid Derived Salicylidenehydrazone Complexes.
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- ChemPhotoChem, 2018, v. 2, n. 12, p. 1038, doi. 10.1002/cptc.201800150
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- Article
Corrigendum: Reversible Lysine Modification on Proteins by Using Functionalized Boronic Acids.
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- Chemistry - A European Journal, 2016, v. 22, n. 47, p. 16711, doi. 10.1002/chem.201503646
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A Three-Component Assembly Promoted by Boronic Acids Delivers a Modular Fluorophore Platform (BASHY Dyes).
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- Chemistry - A European Journal, 2016, v. 22, n. 5, p. 1537, doi. 10.1002/chem.201504919
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Cover Picture: A Three-Component Assembly Promoted by Boronic Acids Delivers a Modular Fluorophore Platform (BASHY Dyes) (Chem. Eur. J. 5/2016).
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- Chemistry - A European Journal, 2016, v. 22, n. 5, p. 1533, doi. 10.1002/chem.201680501
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- Article
A Three-Component Assembly Promoted by Boronic Acids Delivers a Modular Fluorophore Platform (BASHY Dyes).
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- Chemistry - A European Journal, 2016, v. 22, n. 5, p. 1631, doi. 10.1002/chem.201503943
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- Article
Reversible Lysine Modification on Proteins by Using Functionalized Boronic Acids.
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- Chemistry - A European Journal, 2015, v. 21, n. 22, p. 8182, doi. 10.1002/chem.201500127
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Modular Assembly of Reversible Multivalent Cancer-Cell-Targeting Drug Conjugates.
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- Angewandte Chemie, 2017, v. 129, n. 32, p. 9474, doi. 10.1002/ange.201703492
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- Article
Cysteinselektive Reaktionen zur Konjugation von Antikörpern.
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- Angewandte Chemie, 2014, v. 126, n. 40, p. 10758, doi. 10.1002/ange.201405702
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Studies on the Preparation of 4-Ethoxyalkyliden and 4-Aminoalkyliden-5(4H)-oxazolones.
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- Synthetic Communications, 2003, v. 33, n. 8, p. 1285, doi. 10.1081/SCC-120018688
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Rabbit derived VL single-domains as promising scaffolds to generate antibody–drug conjugates.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-31568-x
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- Article
Ring-Expansion Reaction of Isatins with Ethyl Diazoacetate Catalyzed by Dirhodium(II)/DBU Metal-Organic System: En Route to Viridicatin Alkaloids.
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- European Journal of Organic Chemistry, 2013, v. 2013, n. 28, p. 6280, doi. 10.1002/ejoc.201300796
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N-Heterocyclic Carbene Dirhodium(II) Complexes as Catalysts for Allylic and Benzylic Oxidations.
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- European Journal of Organic Chemistry, 2013, v. 2013, n. 8, p. 1471, doi. 10.1002/ejoc.201201300
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Stereo- and Regiocontrol in the Formation of Lactams by Rhodium-Carbenoid C−H Insertion of α-Diazoacetamides.
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- European Journal of Organic Chemistry, 2004, v. 2004, n. 18, p. 3773, doi. 10.1002/ejoc.200400237
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Regio- and Stereoselective Dirhodium(II)-Catalysed Intramolecular C−H Insertion Reactions of α-Diazo-α-(dialkoxyphosphoryl)acetamides and -acetates.
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- European Journal of Organic Chemistry, 2003, v. 2003, n. 19, p. 3798, doi. 10.1002/ejoc.200300330
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Modular Assembly of Reversible Multivalent Cancer-Cell-Targeting Drug Conjugates.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 32, p. 9346, doi. 10.1002/anie.201703492
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Cysteine-Selective Reactions for Antibody Conjugation.
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- Angewandte Chemie International Edition, 2014, v. 53, n. 40, p. 10585, doi. 10.1002/anie.201405702
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