Synthesis of Flavones from the Hypervalent Iodine Oxidation of Flavanones Using [Hydroxy(tosyloxy)iodo]benzene in Methanol
- 1 May 1990
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 20 (10) , 1417-1422
- https://doi.org/10.1080/00397919008052857
Abstract
Hypervalent iodine oxidation of several flavanones (1a-1f) using (hydroxy(tosyloxy)iodo] benzene in methanol offers a new method for the synthesis of flavones (2a-2f).Keywords
This publication has 10 references indexed in Scilit:
- Hypervalent Iodine Oxidation of Flavonols Using [Hydroxy(tosyloxy)iodo]benzebe in MethanolHETEROCYCLES, 1986
- Use of hypervalent iodine oxidation for the C(3)‐hydroxylation of chromone, flavone and α‐naphthoflavoneJournal of Heterocyclic Chemistry, 1985
- Solvohyperiodination. A comparison with solvothallationTetrahedron Letters, 1985
- Hypervalent iodine oxidation of flavanone. Synthesis of cis- and trans-3-hydroxyflavanonesThe Journal of Organic Chemistry, 1985
- Hypervalent iodine oxidation of α,β-unsaturated ketones: chromone, flavone, chalcone, and flavanoneJournal of the Chemical Society, Chemical Communications, 1984
- Oxidation of Flavanones with Thallium(III) Nitrate(ttn). A Convenient Route to FlavonesSynthetic Communications, 1982
- Hypervalent organoiodine. Crystal structure of phenylhydroxytosyloxyiodineThe Journal of Organic Chemistry, 1976
- 664. Synthesis of 6-halogenoflavones and related compoundsJournal of the Chemical Society, 1961
- 234. Reaction of primary amines with o-hydroxydibenzoylmethanes, and the preparation of derivatives of flavone imineJournal of the Chemical Society, 1952
- 195. Synthetical experiments in the chromone group. Part XVI. Chalkones and flavanones and their oxidation to flavones by means of selenium dioxideJournal of the Chemical Society, 1935