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Strain-Promoted Azide-Alkyne Cycloaddition SPAAC Reactions

POC-click is formed by thermo-cross-linking the mixture of pre-POC-N (azide-containing POC prepolymer) and pre-POC-Al (alkyne-containing POC prepolymer) the process applies synchronous binary cross-link mechanism, esterification, and thermal click reaction, and the residual azide groups on the surface of POC-click film or scaffold paved the way of surface bioconjugation through strain-promoted alkyne-azide cycloaddition (SPAAC), another copper-free click reaction. [Pg.263]

Strain-Promoted Azide-Alkyne Cycloaddition (SPAAC) Reactions... [Pg.8]

Strain-promoted azide-alkyne cycloaddition (SPAAC), since its inception in 2004, has firmly established itself as a powerful click chemistry tool. The commercial access of starting materials, its ease of operation, the nowadays practical reaction... [Pg.75]

Fig. 1 Cycloaddition reactions employed in nucleic acid labeling with reporter groups (green star). A Cu -mediated azide-alkyne cycloaddition (CuAAC) of a terminal alkyne with an azide. B Strain-promoted azide-alkyne cycloaddition (SPAAC) of an azide with a cyclooctyne derivative. C Staudinger ligation of an azide with a phosphine derivative (not a cycloaddition reaction, see below). D Norbornene cycloaddition of a nitrile oxide as 1,3-dipole and a norbornene as dipolarophile. E Inverse electron-demand Diels- Alder cycloaddition reaction between a strained double bond (norbornene) and a tetrazine derivative. F Photo-cUck reaction of a push-pull-substituted diaiyltetrazole with an activated double bond (maleimide)... Fig. 1 Cycloaddition reactions employed in nucleic acid labeling with reporter groups (green star). A Cu -mediated azide-alkyne cycloaddition (CuAAC) of a terminal alkyne with an azide. B Strain-promoted azide-alkyne cycloaddition (SPAAC) of an azide with a cyclooctyne derivative. C Staudinger ligation of an azide with a phosphine derivative (not a cycloaddition reaction, see below). D Norbornene cycloaddition of a nitrile oxide as 1,3-dipole and a norbornene as dipolarophile. E Inverse electron-demand Diels- Alder cycloaddition reaction between a strained double bond (norbornene) and a tetrazine derivative. F Photo-cUck reaction of a push-pull-substituted diaiyltetrazole with an activated double bond (maleimide)...
Describe the main criteria that should be satis ed for a reaction to be called a click reaction How would you justify the inclusion of the following reactions into the pantheon of click reactions (a) Copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) reactions (b) strain-promoted azide-alkyne coupling (SPAAC) reactions (c) Diels-Alder (DA) cycloaddition reactions (d) thiol-ene (TE) reactions and (e) thiol-yne (TY) reactions ... [Pg.722]

Generation of chemical patterns with photoreactive polymers photo-Diels-Alder surface anchoring followed by azide-alkyne click reaction to immobilize fluorescent dyes, (a) SPAAC strain-promoted azide-alkyne cycloaddition and (b) CuAAC Cu(l)-catalyzed azide-alkyne cycloaddition. (Source Adapted with permission from Reference [36d].)... [Pg.116]

Sequential click strategies were utihzed by Zhang, Cheng, and coworkers to precisely construct new surfactants based on polyhedral oligomeric silsesquiox-ane (POSS), tethering cychc polymers [109]. The general synthetic approach involves different types of click chemistries sequentially performed strain-promoted azide-alkyne cycloaddition (SPAAC), CuAAC for POSS—polymer conjugation, and thiol-ene reactions for POSS surface functionalization. [Pg.303]


See other pages where Strain-Promoted Azide-Alkyne Cycloaddition SPAAC Reactions is mentioned: [Pg.267]    [Pg.112]    [Pg.466]    [Pg.76]    [Pg.248]    [Pg.9]    [Pg.18]    [Pg.32]    [Pg.60]    [Pg.65]    [Pg.65]    [Pg.138]    [Pg.142]    [Pg.663]    [Pg.34]    [Pg.43]    [Pg.239]   
See also in sourсe #XX -- [ Pg.8 , Pg.239 , Pg.312 , Pg.318 , Pg.328 ]




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Alkyne azide reactions

Alkynes 2+2]-cycloadditions

Alkynes cycloaddition

Alkynes cycloaddition reactions

Azidation reaction

Azide-Alkyne Cycloaddition

Azides cycloaddition

Azides cycloadditions

Azides, reactions

Cycloaddition reactions strain-promoted

Promoters reaction

SPAAC

SPAAC cycloaddition

Strain reaction

Strain-promoted azide-alkyne

Strain-promoted azide-alkyne cycloaddition

Strain-promoted azide-alkyne cycloaddition SPAAC)

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