Author:
Loder JW,Eibl R,Falkiner MJ,Nearn RH,Parr RW
Abstract
Racemic and optical isomers
of 7-hydroxy-3-(p-hydroxyphenyl)-3,4- dihydronaphthalen-1(2H)-one (1) have been
synthesized and the configurations of the optical isomers assigned by o.r.d. spectrometry. Derivatives of these
3,4-dihydronaphthalen-1(2H)-ones with aminooxyacetic acid were prepared and the
1,2,3,4-tetrahydronaphthalene (24) corresponding to (1) was synthesized.
Cited by
3 articles.
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1. The Structure and Function of Estrogens .10. Synthesis of 5,5-Dimethyl-Cis-4b,5,6,10b,11,12-Hexahydrochrysene-2,8-Diol - the Estrogenic Activity of This and of Related C-Methylated Hydrochrysenediols;Australian Journal of Chemistry;1988
2. Immunization of sheep to block the effects of ingested or administered phyto-oestrogens;Toxicon;1983-01
3. Synthesis of 5-p-hydroxybenzyl-5,6-dihydro-2-naphthol, (±)-sequirin D;J. Chem. Soc., Perkin Trans. 1;1981