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Search for "click conjugations" in Full Text gives 2 result(s) in Beilstein Journal of Organic Chemistry.

Investigation of the action of poly(ADP-ribose)-synthesising enzymes on NAD+ analogues

  • Sarah Wallrodt,
  • Edward L. Simpson and
  • Andreas Marx

Beilstein J. Org. Chem. 2017, 13, 495–501, doi:10.3762/bjoc.13.49

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  • ARTD2 catalysed PAR production [24]. After the times indicated, copper-catalysed click conjugations to a fluorophore-containing azide were performed and the reactions were analysed by SDS PAGE. Then, fluorescent signals were detected and compared to the Coomassie Blue stained gels (Figure 2). Each
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Published 10 Mar 2017

Design and synthesis of multivalent neoglycoconjugates by click conjugations

  • Feiqing Ding,
  • Li Ji,
  • Ronny William,
  • Hua Chai and
  • Xue-Wei Liu

Beilstein J. Org. Chem. 2014, 10, 1325–1332, doi:10.3762/bjoc.10.134

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  • hydroamination/glycosylation on glycal scaffolds has been developed to form propargyl 3-tosylamino-2,3-dideoxysugars in a one-pot manner. Subsequent construction of multivalent 3-tosylamino-2,3-dideoxyneoglycoconjugates with potential biochemical applications was presented herein involving click conjugations as
  • the key reaction step. The copper-catalyzed regioselective click reaction was tremendously accelerated with assistance of microwave irradiation. Keywords: click conjugations; copper-catalyzed; microwave irradiation; multivalent glycosystems; neoglycoconjugates; one-pot; Introduction Oligosaccharides
  • /glycosylation of the glycal shown in Figure 1 [49][50][51][52][53]. Extending the synthetic utility of this protocol, herein, we wish to report the synthetic modification of α-GalNAc-linked glycopeptides to 3-tosylamino-2,3-dideoxyneoglycoconjugates via click conjugations (Figure 2). Given the success in using
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Published 10 Jun 2014
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