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Elsevier, Tetrahedron: Asymmetry, 6(21), p. 756-761

DOI: 10.1016/j.tetasy.2010.04.020

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Microwave-assisted regioselective synthesis and isomerization of 6- O-vanillyl- and 6- O- iso-vanillyl hexoses and studies of their activities as radical scavengers by EPR spectroscopy

Journal article published in 2010 by Zuzana Hricovíniová, Michal Zalibera ORCID, Miloš Hricovíni
This paper is available in a repository.
This paper is available in a repository.

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Abstract

Four 6-O-substituted saccharides, namely 6-O-vanillyl-d-glucose 1, 6-O-vanillyl-d-mannose 2, 6-O-iso-vanillyl-d-glucose 3 and 6-O-iso-vanillyl-d-mannose 4 have been synthesized. Synthesized saccharide derivatives have been subsequently used in Mo(VI)-catalyzed stereospecific isomerizations yielding compounds with potential radical scavenging activity. In order to accelerate intramolecular isomerization rates and conversions microwave irradiation was used. Synthesized products were obtained with excellent stereoselectivity in good conversions and were tested by EPR spectroscopy for radical scavenging activity.