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A novel approach to aminocyclitol analogues from azidotrideoxyhex-5-enopyranosides

István F. Pelyvás, Ferenc Sztaricskai, R. Bognár

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Abstract

Application of the Ferrier's carbocyclic ring closure to methyl 3-azido-2,3,6-trideoxyhex-5-enopyranosides leads to cyclitol derivatives (3)and (5) suitable for the convenient synthesis of 1,3-diaminocyclitol -type aminoglycoside antibiotic analogues.

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What this paper is about

Application of the Ferrier's carbocyclic ring closure to methyl 3-azido-2,3,6-trideoxyhex-5-enopyranosides leads to cyclitol derivatives (3)and (5) suitable for the convenient synthesis of 1,3-diaminocyclitol -type aminoglycoside antibiotic analogues.

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OpenAlex reports 12 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available abstract

Application of the Ferrier's carbocyclic ring closure to methyl 3-azido-2,3,6-trideoxyhex-5-enopyranosides leads to cyclitol derivatives (3)and (5) suitable for the convenient synthesis of 1,3-diaminocyclitol -type aminoglycoside antibiotic analogues.

Key concepts: Aminocyclitol, Cyclitol, Chemistry, Aminoglycoside, Ring (chemistry), Stereochemistry, Antibiotics, Organic chemistry

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A novel approach to aminocyclitol analogues from azidotrideoxyhex-5-enopyranosides — Research Paper | ScholarLens