Literature DB >> 24519721

Tunable acid-sensitive ester protecting groups in oligosaccharide synthesis.

Yao Li1, Xinyu Liu.   

Abstract

A series of acid-cleavable ester-type protecting groups, with acid-sensitivity profiles parallel to those of 2-naphthylmethyl (NAP) or p-methoxybenzyl (PMB) ether, were designed and TFA in toluene was identified as a technically simple and effective deblocking cocktail for their global removal in the context of oligosaccharide synthesis.

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Year:  2014        PMID： 24519721     DOI： 10.1039/c3cc49205b

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN： 1359-7345            Impact factor:   6.222


  4 in total

1.  Synthesis of a Glycosylphosphatidylinositol Anchor Derived from Leishmania donovani That Can Be Functionalized by Cu-Catalyzed Azide-Alkyne Cycloadditions.

Authors:  Ning Ding; Xiuru Li; Zoeisha S Chinoy; Geert-Jan Boons
Journal:  Org Lett       Date:  2017-07-11       Impact factor: 6.005

2.  Mild Method for 2-Naphthylmethyl Ether Protecting Group Removal Using a Combination of 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) and β-Pinene.

Authors:  Dina Lloyd; Marissa Bylsma; Danielle K Bright; Xizhao Chen; Clay S Bennett
Journal:  J Org Chem       Date:  2017-03-27       Impact factor: 4.354

3.  Competition-driven selection in covalent dynamic networks and implementation in organic reactional selectivity.

Authors:  P Kovaříček; A C Meister; K Flídrová; R Cabot; K Kovaříčková; J-M Lehn
Journal:  Chem Sci       Date:  2016-02-10       Impact factor: 9.825

4.  Synthesis of monophosphorylated lipid A precursors using 2-naphthylmethyl ether as a protecting group.

Authors:  Jundi Xue; Ziyi Han; Gen Li; Khalisha A Emmanuel; Cynthia L McManus; Qiang Sui; Dongmian Ge; Qi Gao; Li Cai
Journal:  Beilstein J Org Chem       Date:  2020-08-10       Impact factor: 2.883
  4 in total

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