Oxidative aza Michael addition of nitrogen-containing heterocycles to kojic acid-derived Baylis-Hillman adducts

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Abstract: The oxidation of Baylis-Hillman adducts, obtained by the reaction of 5-benzyloxy-2-formyl-4-pyrone, with o-iodoxybenzoic acid generates β-ketomethylene intermediates that in situ undergo conjugative attack of NH-containing heterocycles such as imidazole and pyrazoles.

Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: Oxidative aza Michael addition of nitrogen-containing heterocycles to kojic acid-derived Baylis-Hillman adducts ; volume:21 ; number:1 ; year:2015 ; pages:37-41 ; extent:5
Heterocyclic communications ; 21, Heft 1 (2015), 37-41 (gesamt 5)

Creator: Ghasemi, Zarrin
Esfangare, Hasan Kalantar

DOI: 10.1515/hc-2014-0197

URN: urn:nbn:de:101:1-2501130542592.241976505208

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:32 AM CEST

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Ghasemi, Zarrin
Esfangare, Hasan Kalantar

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Oxidative aza Michael addition of nitrogen-containing heterocycles to kojic acid-derived Baylis-Hillman adducts

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Other Objects (12)

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