Potassium-Catalyzed Reactions of β-Alkylstyrenes and Anethol with Alkylbenzenes1
J Shabtai, EM Lewicki, H Pines
Index: Shabtai,J. et al. Journal of Organic Chemistry, 1962 , vol. 27, p. 2618 - 2621
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Citation Number: 6
Abstract
&Methyl-, @-ethyl-, and @-isopropylstyrene react with toluene at 110" in the presence of dispersed potassiuni to form the corresponding 1,3-diphenyl-2-alkylpropsnes in 60-9545 yields. Anethol reacts similarly to form 1-p-methoxyphenyl-2-meth- yl-3-phenylpropane in 68% yield. P,&Dimethylstyrene, however, fails to react with toluene. @-Ethylstyrene undergoes also ring closure with the formation of 1-methylindenr. ... It was reported recently that ...
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[Shabtai,J.; Pines,H. Journal of Organic Chemistry, 1964 , vol. 29, p. 2408 - 2412]