A high‐yield modification of the baker‐venkataraman rearrangement. Application to the synthesis of 5‐hydroxyflavone and 6,8‐dichloro‐5‐hydroxyflavone
- 1 July 1964
- journal article
- research article
- Published by Wiley in Journal of Heterocyclic Chemistry
- Vol. 1 (3) , 141-144
- https://doi.org/10.1002/jhet.5570010308
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Physical and Chemical Properties of Hydroxyflavones. II. 3-Aroyl-5-hydroxyflavones. Synthetic and Infrared Spectral Studies1,2The Journal of Organic Chemistry, 1962
- Physical and Chemical Properties of Hydroxyflavones. I. Infrared Absorption Spectra of Monohydroxyflavones and Their O-Methyl and O-Acetyl Derivatives1,2The Journal of Organic Chemistry, 1962
- Chelate systems. Part III. Infrared spectra of flavanones and flavonesJournal of the Chemical Society, 1955
- Nuclear oxidation in the flavone seriesProceedings of the Indian Academy of Sciences - Section A, 1947
- Über ein natürliches Vorkommen des 5‐OxyflavonsHelvetica Chimica Acta, 1940
- 204. The synthesis of 5 : 6-dihydroxyflavone and the structure of primetinJournal of the Chemical Society, 1939
- 429. Attempts to synthesise 5 : 6-dihydroxyflavone (primetin)Journal of the Chemical Society, 1934
- 319. The synthesis of 5-hydroxyflavoneJournal of the Chemical Society, 1934
- 322. Molecular rearrangement of some o-acyloxyacetophenones and the mechanism of the production of 3-acylchromonesJournal of the Chemical Society, 1933
- CCXC.—An accessible derivative of chromonolJournal of the Chemical Society, Transactions, 1924