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1
Azide/Alkyne-"Click"-Reactions of Encapsulated Reagents: Toward Self-Healing Materials
Azide/Alkyne-"Click"-Reactions of Encapsulated Reagents: Toward Self-Healing Materials
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Azide/Alkyne-"Click"-Reactions of Encapsulated Reagents: Toward Self-Healing Materials

Macromolecular rapid communications., 2011-03, Vol.32 (5), p.419-425 [Peer Reviewed Journal]

Copyright © 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. ;ISSN: 1022-1336 ;ISSN: 1521-3927 ;EISSN: 1521-3927 ;DOI: 10.1002/marc.201000687 ;PMID: 21433193

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2
Efficient Access to New Chemical Space Through Flow-Construction of Druglike Macrocycles Through Copper-Surface-Catalyzed Azide-Alkyne Cycloaddition Reactions
Efficient Access to New Chemical Space Through Flow-Construction of Druglike Macrocycles Through Copper-Surface-Catalyzed Azide-Alkyne Cycloaddition Reactions
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Efficient Access to New Chemical Space Through Flow-Construction of Druglike Macrocycles Through Copper-Surface-Catalyzed Azide-Alkyne Cycloaddition Reactions

Chemistry : a European journal, 2010-12, Vol.16 (48), p.14506-14512 [Peer Reviewed Journal]

Copyright © 2010 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 0947-6539 ;ISSN: 1521-3765 ;EISSN: 1521-3765 ;DOI: 10.1002/chem.201002215 ;PMID: 21038332 ;CODEN: CEUJED

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3
Click chemistry in peptide-based drug design
Click chemistry in peptide-based drug design
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Click chemistry in peptide-based drug design

Molecules, 2013-08, Vol.18 (8), p.9797-9817 [Peer Reviewed Journal]

Copyright MDPI AG 2013 ;2013 by the authors; licensee MDPI, Basel, Switzerland. 2013 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules18089797 ;PMID: 23959192

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4
A real-time, click chemistry imaging approach reveals stimulus-specific subcellular locations of phospholipase D activity
A real-time, click chemistry imaging approach reveals stimulus-specific subcellular locations of phospholipase D activity
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A real-time, click chemistry imaging approach reveals stimulus-specific subcellular locations of phospholipase D activity

Proceedings of the National Academy of Sciences - PNAS, 2019-07, Vol.116 (31), p.15453-15462 [Peer Reviewed Journal]

Copyright National Academy of Sciences Jul 30, 2019 ;2019 ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.1903949116 ;PMID: 31311871

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5
An artificial triazole backbone linkage provides a split-and-click strategy to bioactive chemically modified CRISPR sgRNA
An artificial triazole backbone linkage provides a split-and-click strategy to bioactive chemically modified CRISPR sgRNA
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An artificial triazole backbone linkage provides a split-and-click strategy to bioactive chemically modified CRISPR sgRNA

Nature communications, 2019-04, Vol.10 (1), p.1610-1610, Article 1610 [Peer Reviewed Journal]

The Author(s) 2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2019 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-019-09600-4 ;PMID: 30962447

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6
Universal inverse design of surfaces with thin nematic elastomer sheets
Universal inverse design of surfaces with thin nematic elastomer sheets
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Universal inverse design of surfaces with thin nematic elastomer sheets

Proceedings of the National Academy of Sciences - PNAS, 2018-07, Vol.115 (28), p.7206-7211 [Peer Reviewed Journal]

Volumes 1–89 and 106–115, copyright as a collective work only; author(s) retains copyright to individual articles ;Copyright National Academy of Sciences Jul 10, 2018 ;2018 ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.1804702115 ;PMID: 29929963

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7
Macrocyclic drugs and synthetic methodologies toward macrocycles
Macrocyclic drugs and synthetic methodologies toward macrocycles
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Macrocyclic drugs and synthetic methodologies toward macrocycles

Molecules, 2013-05, Vol.18 (6), p.6230-6268 [Peer Reviewed Journal]

Copyright MDPI AG 2013 ;2013 by the authors; licensee MDPI, Basel, Switzerland. 2013 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules18066230 ;PMID: 23708234

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8
The click reaction as an efficient tool for the construction of macrocyclic structures
The click reaction as an efficient tool for the construction of macrocyclic structures
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The click reaction as an efficient tool for the construction of macrocyclic structures

Molecules, 2013-08, Vol.18 (8), p.9512-9530 [Peer Reviewed Journal]

Copyright MDPI AG 2013 ;2013 by the authors; licensee MDPI, Basel, Switzerland. 2013 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules18089512 ;PMID: 23966075

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9
Organocatalytic Enamide-Azide Cycloaddition Reactions: Regiospecific Synthesis of 1,4,5-Trisubstituted-1,2,3-Triazoles
Organocatalytic Enamide-Azide Cycloaddition Reactions: Regiospecific Synthesis of 1,4,5-Trisubstituted-1,2,3-Triazoles
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Organocatalytic Enamide-Azide Cycloaddition Reactions: Regiospecific Synthesis of 1,4,5-Trisubstituted-1,2,3-Triazoles

Chemistry : a European journal, 2011-03, Vol.17 (13), p.3584-3587 [Peer Reviewed Journal]

Copyright © 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 0947-6539 ;EISSN: 1521-3765 ;DOI: 10.1002/chem.201002775 ;PMID: 21341323 ;CODEN: CEUJED

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10
Exploiting Protein N-Terminus for Site-Specific Bioconjugation
Exploiting Protein N-Terminus for Site-Specific Bioconjugation
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Exploiting Protein N-Terminus for Site-Specific Bioconjugation

Molecules (Basel, Switzerland), 2021-06, Vol.26 (12), p.3521 [Peer Reviewed Journal]

2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2021 by the authors. 2021 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules26123521 ;PMID: 34207845

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11
Polysaccharides: The “Click” Chemistry Impact
Polysaccharides: The “Click” Chemistry Impact
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Polysaccharides: The “Click” Chemistry Impact

Polymers, , Vol.3 (4), p.1607-1651 [Peer Reviewed Journal]

Copyright MDPI AG 2011 ;ISSN: 2073-4360 ;EISSN: 2073-4360 ;DOI: 10.3390/polym3041607

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12
A Click–Click Approach for the Preparation of Functionalized [5:1]‐Hexaadducts of C60
A Click–Click Approach for the Preparation of Functionalized [5:1]‐Hexaadducts of C60
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A Click–Click Approach for the Preparation of Functionalized [5:1]‐Hexaadducts of C60

Chemistry : a European journal, 2009-07, Vol.15 (30), p.7306-7309 [Peer Reviewed Journal]

Copyright © 2009 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 0947-6539 ;EISSN: 1521-3765 ;DOI: 10.1002/chem.200901291 ;PMID: 19579241

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13
Advances in click chemistry for single-chain nanoparticle construction
Advances in click chemistry for single-chain nanoparticle construction
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Advances in click chemistry for single-chain nanoparticle construction

Molecules, 2013-03, Vol.18 (3), p.3339-3355 [Peer Reviewed Journal]

Copyright MDPI AG 2013 ;2013 by the authors; licensee MDPI, Basel, Switzerland. 2013 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules18033339 ;PMID: 23493101

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14
Simultaneous ultrasound- and microwave-assisted one-pot ‘click’ synthesis of 3-formyl-indole clubbed 1,2,3-triazole derivatives and their biological evaluation
Simultaneous ultrasound- and microwave-assisted one-pot ‘click’ synthesis of 3-formyl-indole clubbed 1,2,3-triazole derivatives and their biological evaluation
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Simultaneous ultrasound- and microwave-assisted one-pot ‘click’ synthesis of 3-formyl-indole clubbed 1,2,3-triazole derivatives and their biological evaluation

Molecular diversity, 2022-04, Vol.26 (2), p.963-979 [Peer Reviewed Journal]

The Author(s), under exclusive licence to Springer Nature Switzerland AG 2021 ;2021. The Author(s), under exclusive licence to Springer Nature Switzerland AG. ;The Author(s), under exclusive licence to Springer Nature Switzerland AG 2021. ;ISSN: 1381-1991 ;EISSN: 1573-501X ;DOI: 10.1007/s11030-021-10212-8 ;PMID: 33834361

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15
Strain-Promoted Alkyne-Azide Cycloadditions (SPAAC) Reveal New Features of Glycoconjugate Biosynthesis
Strain-Promoted Alkyne-Azide Cycloadditions (SPAAC) Reveal New Features of Glycoconjugate Biosynthesis
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Strain-Promoted Alkyne-Azide Cycloadditions (SPAAC) Reveal New Features of Glycoconjugate Biosynthesis

Chembiochem : a European journal of chemical biology, 2011-08, Vol.12 (12), p.1912-1921 [Peer Reviewed Journal]

Copyright © 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. ;ISSN: 1439-4227 ;EISSN: 1439-7633 ;DOI: 10.1002/cbic.201100117 ;PMID: 21661087

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16
Click Chemistry: 1,2,3-Triazoles as Pharmacophores
Click Chemistry: 1,2,3-Triazoles as Pharmacophores
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Click Chemistry: 1,2,3-Triazoles as Pharmacophores

Chemistry, an Asian journal, 2011-10, Vol.6 (10), p.2696-2718 [Peer Reviewed Journal]

Copyright © 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. ;ISSN: 1861-4728 ;EISSN: 1861-471X ;DOI: 10.1002/asia.201100432 ;PMID: 21954075

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17
To View Your Biomolecule, Click inside the Cell
To View Your Biomolecule, Click inside the Cell
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To View Your Biomolecule, Click inside the Cell

Angewandte Chemie International Edition, 2021-10, Vol.60 (43), p.23084-23105 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.202101502

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18
SuFEx-enabled, agnostic discovery of covalent inhibitors of human neutrophil elastase
SuFEx-enabled, agnostic discovery of covalent inhibitors of human neutrophil elastase
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SuFEx-enabled, agnostic discovery of covalent inhibitors of human neutrophil elastase

Proceedings of the National Academy of Sciences - PNAS, 2019-09, Vol.116 (38), p.18808-18814 [Peer Reviewed Journal]

Copyright National Academy of Sciences Sep 17, 2019 ;2019 ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.1909972116 ;PMID: 31484779

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19
Click Chemistry as a Tool for Cell Engineering and Drug Delivery
Click Chemistry as a Tool for Cell Engineering and Drug Delivery
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Click Chemistry as a Tool for Cell Engineering and Drug Delivery

Molecules (Basel, Switzerland), 2019-01, Vol.24 (1), p.172 [Peer Reviewed Journal]

2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2019 by the authors. 2019 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules24010172 ;PMID: 30621193

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20
Click Chemistry-mediated Biotinylation Reveals a Function for the Protease BACE1 in Modulating the Neuronal Surface Glycoproteome
Click Chemistry-mediated Biotinylation Reveals a Function for the Protease BACE1 in Modulating the Neuronal Surface Glycoproteome
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Click Chemistry-mediated Biotinylation Reveals a Function for the Protease BACE1 in Modulating the Neuronal Surface Glycoproteome

Molecular & cellular proteomics, 2018-08, Vol.17 (8), p.1487-1501 [Peer Reviewed Journal]

2018 © 2018 Herber et al. ;2018 Herber et al. ;Copyright American Society for Biochemistry and Molecular Biology Aug 2018 ;2018 Herber et al. 2018 Herber et al. ;ISSN: 1535-9476 ;EISSN: 1535-9484 ;DOI: 10.1074/mcp.RA118.000608 ;PMID: 29716987

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