Polypropylene-based graft copolymers via CuAAC click chemistry
نویسندگان
چکیده
منابع مشابه
Peptide conjugation via CuAAC 'click' chemistry.
The copper (I)-catalyzed alkyne azide 1,3-dipolar cycloaddition (CuAAC) or 'click' reaction, is a highly versatile reaction that can be performed under a variety of reaction conditions including various solvents, a wide pH and temperature range, and using different copper sources, with or without additional ligands or reducing agents. This reaction is highly selective and can be performed in th...
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Click chemistry is an approach that uses efficient and reliable reactions, such as Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC), to bind two molecular building blocks. CuAAC has broad applications in medicinal chemistry and other fields of chemistry. This review describes the general features and applications of CuAAC in solid-phase synthesis (CuAAC-SP), highlighting the suitability of th...
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Synthesis, characterization, and properties of new thermally curable polysulfone containing benzoxazine moieties in the side chain were investigated. First, chloromethylation and subsequent azidation processes were performed to form polysulfone containing pendant clickable azide groups. Independently, antagonist 3,4-dihydro-3-(prop-2-ynyl)-2H-benzoxazine was prepared by using paraformaldehyde, ...
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A Cu-catalysed macrocyclisation was performed to obtain a macrocyclic coumarin-containing tripeptide for use in thrombin activity measurements.
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Heterotelechelic polystyrene (PS), poly(tert-butyl acrylate) (PtBA), and poly (methyl acrylate) (PMA), containing both azide and triisopropylsilyl (TIPS) protected acetylene end groups, were prepared in good control (Mw/Mn 1.24) by atom transfer radical polymerization (ATRP). The end groups were independently applied in two successive ‘‘click’’ reactions, that is: first the azide termini were f...
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ژورنال
عنوان ژورنال: Express Polymer Letters
سال: 2018
ISSN: 1788-618X
DOI: 10.3144/expresspolymlett.2018.35