We synthesized fused bicyclic polyfunctional compounds containing a highly hydroxylated pyran ring starting from commercially available methyl glucopyranoside and adopting a RCM annulation approach. The versatile α,β-unsaturated ketone group was introduced on the newly formed ring and, as an example of the potential of these polyfunctionalized building blocks, a tetracyclic compound was synthesized through a Diels-Alder cycloaddition reaction

Cardona, F., D'Orazio, G., Silva, A., Nicotra, F., LA FERLA, B. (2014). Synthesis of glyco-Fused Bicyclic Compounds: Conformationally Constrained Scaffolds and Useful Polyfunctional Building Blocks. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2014(12), 2549-2556 [10.1002/ejoc.201400028].

Synthesis of glyco-Fused Bicyclic Compounds: Conformationally Constrained Scaffolds and Useful Polyfunctional Building Blocks

D'ORAZIO, GIUSEPPE;NICOTRA, FRANCESCO;LA FERLA, BARBARA
2014

Abstract

We synthesized fused bicyclic polyfunctional compounds containing a highly hydroxylated pyran ring starting from commercially available methyl glucopyranoside and adopting a RCM annulation approach. The versatile α,β-unsaturated ketone group was introduced on the newly formed ring and, as an example of the potential of these polyfunctionalized building blocks, a tetracyclic compound was synthesized through a Diels-Alder cycloaddition reaction
Articolo in rivista - Articolo scientifico
Annulation; Chiral pool; Cycloaddition; Diastereoselectivity; Glycoconjugates; Synthetic methods;
Chiral Pool, Diastereoselectivity, synthetic methods, glycoconjugates, annulation, cycloaddition
English
2014
2014
12
2549
2556
none
Cardona, F., D'Orazio, G., Silva, A., Nicotra, F., LA FERLA, B. (2014). Synthesis of glyco-Fused Bicyclic Compounds: Conformationally Constrained Scaffolds and Useful Polyfunctional Building Blocks. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2014(12), 2549-2556 [10.1002/ejoc.201400028].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/51344
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