The synthesis of novel hyperbranched monodisperse linear dendrimers, based on 2,2-bis-(hydroxymethyl)-propionic acid (bis-MPA), has been achieved by convergent metathesis-mediated coupling between the alkene-terminated focal point of bis-MPA dendrons. On their surface, dendrimers present 4, 8 and 16 functional groups. Glycodendrimers exposing multiple saccharide moieties have also been obtained. To the best of our knowledge, this is the first example of the use of metathesis for focal point coupling.

Guizzardi, R., Vacchini, M., Santambrogio, C., Cipolla, L. (2017). Convergent dendrimer synthesis by olefin metathesis and studies toward glycoconjugation. CANADIAN JOURNAL OF CHEMISTRY, 95(9), 1008-1012 [10.1139/cjc-2017-0146].

Convergent dendrimer synthesis by olefin metathesis and studies toward glycoconjugation

GUIZZARDI, ROBERTO
Primo
;
VACCHINI, MATTIA
Secondo
;
SANTAMBROGIO, CARLO
Penultimo
;
CIPOLLA, LAURA FRANCESCA
Ultimo
2017

Abstract

The synthesis of novel hyperbranched monodisperse linear dendrimers, based on 2,2-bis-(hydroxymethyl)-propionic acid (bis-MPA), has been achieved by convergent metathesis-mediated coupling between the alkene-terminated focal point of bis-MPA dendrons. On their surface, dendrimers present 4, 8 and 16 functional groups. Glycodendrimers exposing multiple saccharide moieties have also been obtained. To the best of our knowledge, this is the first example of the use of metathesis for focal point coupling.
Articolo in rivista - Articolo scientifico
dendrimers, glycodendrimers, olefin metathesis, alkoxyamino-carbonyl chemistry
English
2017
95
9
1008
1012
none
Guizzardi, R., Vacchini, M., Santambrogio, C., Cipolla, L. (2017). Convergent dendrimer synthesis by olefin metathesis and studies toward glycoconjugation. CANADIAN JOURNAL OF CHEMISTRY, 95(9), 1008-1012 [10.1139/cjc-2017-0146].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/168595
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