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Search for "photocleavable linker" in Full Text gives 4 result(s) in Beilstein Journal of Organic Chemistry.

Linker, loading, and reaction scale influence automated glycan assembly

  • Marlene C. S. Dal Colle,
  • Manuel G. Ricardo,
  • Nives Hribernik,
  • José Danglad-Flores,
  • Peter H. Seeberger and
  • Martina Delbianco

Beilstein J. Org. Chem. 2023, 19, 1015–1020, doi:10.3762/bjoc.19.77

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  • purification steps. Keywords: automated glycan assembly; photocleavable linker; polysaccharides; solid-phase synthesis; Introduction Automated glycan assembly (AGA) is a solid-phase method that enables the rapid synthesis of complex oligo- and polysaccharides from protected monosaccharide building blocks
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Letter
Published 06 Jul 2023

Automated glycan assembly of arabinomannan oligosaccharides from Mycobacterium tuberculosis

  • Alonso Pardo-Vargas,
  • Priya Bharate,
  • Martina Delbianco and
  • Peter H. Seeberger

Beilstein J. Org. Chem. 2019, 15, 2936–2940, doi:10.3762/bjoc.15.288

Graphical Abstract
  • required to access all six oligosaccharides, ranging from hexa- to dodecasaccharides. Results and Discussion The automated syntheses of oligomannosides 4–6 and oligoarabinomannosides 7–9 were performed on a self-built automated synthesizer using a Merrifield resin functionalized with a photocleavable
  • linker as solid support [25]. A typical AGA cycle consisted of three modules. The acidic wash module prepared the resin for glycosylation by quenching any remaining base from a previous cycle. In the glycosylation module, the thioglycoside donor was coupled to the resin upon activation with NIS and TfOH
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Full Research Paper
Published 06 Dec 2019

Stimuli-responsive oligonucleotides in prodrug-based approaches for gene silencing

  • Françoise Debart,
  • Christelle Dupouy and
  • Jean-Jacques Vasseur

Beilstein J. Org. Chem. 2018, 14, 436–469, doi:10.3762/bjoc.14.32

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Review
Published 19 Feb 2018

Automated solid-phase synthesis of oligosaccharides containing sialic acids

  • Chian-Hui Lai,
  • Heung Sik Hahm,
  • Chien-Fu Liang and
  • Peter H. Seeberger

Beilstein J. Org. Chem. 2015, 11, 617–621, doi:10.3762/bjoc.11.69

Graphical Abstract
  • automated method for chemical sialylation. Monosaccharide building blocks 4, 5 [14], 6, 7 [21], 8, 9 [21], and 10 [5] were employed for these syntheses. Merrifield polystyrene resin equipped with a photocleavable linker, 11, was placed in the reaction chamber of the automated synthesizer and the coupling
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Published 04 May 2015
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