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Two-color emissive probes for click reactions
Chem. Commun., 2014CuAAC is visualized using a BODIPY reaction system by the bathochromic shift of the fluorescence wavelength in ensemble and microscopy experiments. Reaction progress is correlated with chromophore elongation fading out disturbing background fluorescence.
Marcel, Wirtz +6 more
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Chemoselective Tyrosine Bioconjugation through Sulfate Click Reaction
Chemistry – A European Journal, 2018AbstractA novel and selective tyrosine functionalization strategy through SuFEx (sulfur fluoride exchange) chemistry is presented. In this approach, free tyrosine (Tyr) reacts selectively with aryl fluorosulfate in the presence of various nucleophilic amino acid residues in bio‐tolerable conditions.
Eun Joung Choi +4 more
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ACS Applied Nano Materials, 2018
In this work, an azido-modified dopamine derivative was synthesized and subsequently used to postfunctionalize the surface of nanoporous poly(styrene)-block-poly(4-vinylpyridine) diblock copolymer membranes.
Christian Höhme +5 more
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In this work, an azido-modified dopamine derivative was synthesized and subsequently used to postfunctionalize the surface of nanoporous poly(styrene)-block-poly(4-vinylpyridine) diblock copolymer membranes.
Christian Höhme +5 more
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A Fluorogenic, Nucleic Acid Directed “Click” Reaction
Inorganic Chemistry, 2009A fluorogenic, nucleic acid directed, Cu(+)-catalyzed chemical reaction was developed that allows sequence-specific detection of nucleic acids at concentrations as low as 20 nM through monitoring of the increase of the fluorescence intensity. A single nucleotide mismatch in the template strand leads to the complete inhibition of this reaction.
Elmar, Jentzsch, Andriy, Mokhir
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Click chemistry under non-classical reaction conditions
Chem. Soc. Rev., 2010First described almost a decade ago, "click" reactions such as the Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC) are widely used today in organic and medicinal chemistry, in the polymer and material science field, and in chemical biology. While most click reactions can be performed at room temperature there are instances where some form of process
C Oliver, Kappe, Erik, Van der Eycken
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Polymer “Clicking” by CuAAC Reactions
Macromolecular Rapid Communications, 2008AbstractThe CuAAC “click” reaction has developed as one of the most useful and widely employed reactions in ligation within polymer chemistry. This is due to the unique properties of the Cu(I) catalysis which renders the reaction quantitative even at low concentrations, orthogonal with other chemistries and extremely robust.
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Recent Fascinating Aspects of the CuAAC Click Reaction
Trends in Chemistry, 2020M. Meldal, F. Diness
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Miscellaneous Click and Click-like Reactions in Polymer Science
Click chemistry approaches have directed the materials research community to access a diverse range of complex polymeric systems. Click chemistry involves exploiting the easy-to-execute chemical reactions that can be performed at ambient conditions while being efficient and rapid.Prantik Mondal +2 more
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Triple Click Reaction Strategy for Macromolecular Diversity
Macromolecular Rapid Communications, 2012AbstractThis Feature Article focuses on the rapidly emerging concept of the “triple click reactions” towards the design and synthesis of macromolecules with well‐defined topology and chemical composition, and also precise molecular weight and narrow molecular weight distribution. The term “triple click reaction” used in this feature article is based on
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การเตรียมหมึกชีวภาพจากเซริซินผ่านปฏิกิริยา thiol-ene click reaction
เซริซิน (Sericin) เป็นโปรตีนที่สร้างขึ้นโดยตัวไหม (Bombyx mori) ในการผลิตรังไหม เซริซินถูกนำมาใช้อย่างหลากหลายทางด้านยาและเครื่องสำอาง ในงานนี้ผู้วิจัยได้กราฟท์หมู่ methacryloyl ลงไปบนเซริซิน (Ser-MA) ด้วยการนำเซริซินไปละลายในพิริดีนและทำปฏิกิริยากับ methacrylic anhydride ซึ่งจะได้เปอร์เซ็นต์การแทนที่เป็น 0.36% จากการวิเคราะห์ด้วยเทคนิค ¹H NMR การกราฟท์openaire +1 more source