Quinones and quinone methides. VII. Reactions of 1,4-naphthoquinone and 1,4-benzoquinones with 4-hydroxy-2H-1-benzopyran-2-one and 5,5-dimethylcyclohexane-1,3-dione in acid solutions
- 1 January 1980
- journal article
- research article
- Published by CSIRO Publishing in Australian Journal of Chemistry
- Vol. 33 (7) , 1603-1610
- https://doi.org/10.1071/ch9801603
Abstract
4-Hydroxy-2H-1-benzopyran-2-one (4) reacts with 1,4-naphthoquinone, 2- methoxy-1,4-benzoquinone and 1,4-benzoquinone in aqueous acetic acid solutions to yield the quinone (6) and the quinols (11)and (2), respectively. With 5,5-dimethylcyclohexane-1,3-dione, 1,4- naphthoquinone forms a bisfurano compound (9) while 1,4-benzoquinone yields the bisfurano compound (18) and the monophenolic furano derivative (17). The blue product formed by acid catalysed dimerization of 2-methoxy-1,4-benzoquinone forms a diacetate, the n.m.r. spectra of which is in accord with structure (15b).Keywords
This publication has 2 references indexed in Scilit:
- Association of coumestanss with tee hypersensitivity of Lima bean roots to Pratylenchus scribneriPhysiological Plant Pathology, 1977
- Estrogenic activity of coumestrol and related compoundsArchives of Biochemistry and Biophysics, 1960