Low-generation dendrimers with a calixarene core and based on a chiral C2-symmetric pyrrolidine as iminosugar mimics
The preparation of low-generation dendrimers based on a simple calix[4]arene scaffold by insertion of the iminosugar-analogue C2-symmetric 3,4-dihydroxypyrrolidine is described. This methodology allows a rapid incorporation of a considerable number of iminosugar-like moieties in a reduced volume and...
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doaj-21bb9d8a95d241729b8495fad9e8197f2021-02-02T04:39:00ZengBeilstein-InstitutBeilstein Journal of Organic Chemistry1860-53972012-06-018195195710.3762/bjoc.8.1071860-5397-8-107Low-generation dendrimers with a calixarene core and based on a chiral C2-symmetric pyrrolidine as iminosugar mimicsMarco Marradi0Stefano Cicchi1Francesco Sansone2Alessandro Casnati3Andrea Goti4Dipartimento di Chimica “Ugo Schiff”, Università degli Studi di Firenze, via della Lastruccia 13, I-50019 Sesto Fiorentino (Firenze), ItalyDipartimento di Chimica “Ugo Schiff”, Università degli Studi di Firenze, via della Lastruccia 13, I-50019 Sesto Fiorentino (Firenze), ItalyDipartimento di Chimica Organica e Industriale, Università degli Studi di Parma, Parco Area delle Scienze 17/A, I-43124 Parma, ItalyDipartimento di Chimica Organica e Industriale, Università degli Studi di Parma, Parco Area delle Scienze 17/A, I-43124 Parma, ItalyDipartimento di Chimica “Ugo Schiff”, Università degli Studi di Firenze, via della Lastruccia 13, I-50019 Sesto Fiorentino (Firenze), ItalyThe preparation of low-generation dendrimers based on a simple calix[4]arene scaffold by insertion of the iminosugar-analogue C2-symmetric 3,4-dihydroxypyrrolidine is described. This methodology allows a rapid incorporation of a considerable number of iminosugar-like moieties in a reduced volume and in a well-defined geometry. The inclusion of alkali-metal ions (sodium and potassium) in the polar cavity defined by the acetamide moieties at the lower rim of the calixarene was demonstrated, which allows also the rigidification of the dendrimer structure and the iminosugar presentation in the clusters. The combination of the supramolecular properties of calixarenes with the advantage of a dendrimeric presentation of repetitive units opens up the possibility of generating well-defined multivalent and multifaceted systems with more complex and/or biologically relevant iminosugars.https://doi.org/10.3762/bjoc.8.107calixarenescation-responsive systemdendrimersiminosugarsmultivalency |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Marco Marradi Stefano Cicchi Francesco Sansone Alessandro Casnati Andrea Goti |
spellingShingle |
Marco Marradi Stefano Cicchi Francesco Sansone Alessandro Casnati Andrea Goti Low-generation dendrimers with a calixarene core and based on a chiral C2-symmetric pyrrolidine as iminosugar mimics Beilstein Journal of Organic Chemistry calixarenes cation-responsive system dendrimers iminosugars multivalency |
author_facet |
Marco Marradi Stefano Cicchi Francesco Sansone Alessandro Casnati Andrea Goti |
author_sort |
Marco Marradi |
title |
Low-generation dendrimers with a calixarene core and based on a chiral C2-symmetric pyrrolidine as iminosugar mimics |
title_short |
Low-generation dendrimers with a calixarene core and based on a chiral C2-symmetric pyrrolidine as iminosugar mimics |
title_full |
Low-generation dendrimers with a calixarene core and based on a chiral C2-symmetric pyrrolidine as iminosugar mimics |
title_fullStr |
Low-generation dendrimers with a calixarene core and based on a chiral C2-symmetric pyrrolidine as iminosugar mimics |
title_full_unstemmed |
Low-generation dendrimers with a calixarene core and based on a chiral C2-symmetric pyrrolidine as iminosugar mimics |
title_sort |
low-generation dendrimers with a calixarene core and based on a chiral c2-symmetric pyrrolidine as iminosugar mimics |
publisher |
Beilstein-Institut |
series |
Beilstein Journal of Organic Chemistry |
issn |
1860-5397 |
publishDate |
2012-06-01 |
description |
The preparation of low-generation dendrimers based on a simple calix[4]arene scaffold by insertion of the iminosugar-analogue C2-symmetric 3,4-dihydroxypyrrolidine is described. This methodology allows a rapid incorporation of a considerable number of iminosugar-like moieties in a reduced volume and in a well-defined geometry. The inclusion of alkali-metal ions (sodium and potassium) in the polar cavity defined by the acetamide moieties at the lower rim of the calixarene was demonstrated, which allows also the rigidification of the dendrimer structure and the iminosugar presentation in the clusters. The combination of the supramolecular properties of calixarenes with the advantage of a dendrimeric presentation of repetitive units opens up the possibility of generating well-defined multivalent and multifaceted systems with more complex and/or biologically relevant iminosugars. |
topic |
calixarenes cation-responsive system dendrimers iminosugars multivalency |
url |
https://doi.org/10.3762/bjoc.8.107 |
work_keys_str_mv |
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