Literature DB >> 21776974

Mannopyranosyl uronic acid donor reactivity.

Marthe T C Walvoort1, Wilbert de Witte, Jesse van Dijk, Jasper Dinkelaar, Gerrit Lodder, Herman S Overkleeft, Jeroen D C Codée, Gijsbert A van der Marel.   

Abstract

The reactivity of a variety of mannopyranosyl uronic acid donors was assessed in a set of competition experiments, in which two (S)-tolyl mannosyl donors were made to compete for a limited amount of promoter (NIS/TfOH). These experiments revealed that the reactivity of mannuronic acid donors is significantly higher than expected based on the electron-withdrawing capacity of the C-5 carboxylic acid ester function. A 4-O-acetyl-β-(S)-tolyl mannuronic acid donor was found to have similar reactivity as per-O-benzyl-α-(S)-tolyl mannose.
© 2011 American Chemical Society

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Year:  2011        PMID: 21776974     DOI: 10.1021/ol2016862

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  6 in total

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Review 4.  Strategies in synthesis of heparin/heparan sulfate oligosaccharides: 2000-present.

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6.  The influence of acceptor nucleophilicity on the glycosylation reaction mechanism.

Authors:  S van der Vorm; T Hansen; H S Overkleeft; G A van der Marel; J D C Codée
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  6 in total

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