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
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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