Khanolkar, A. P. ; Wheeler , T. S. (1938) Chalkones: synthesis of 1-p-alkoxyarylidene-5 : 6-benzocoumaran-2-ones Journal of the Chemical Society . pp. 2118-2119. ISSN 0368-1769
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Official URL: http://pubs.rsc.org/en/content/articlelanding/1938...
Related URL: http://dx.doi.org/10.1039/JR9380002118
Abstract
l-Hydroxy-2-naphthyl p-alkoxystyryl ketone dibromides, ahich normally yield flavones with alcoholic alkali, give b-alkoxy-compounds and then arylidenecou-maranones, if the solubility of the dibromide in alcohols is increased by addition of chloroform. With aqueous alkali and acetone the dibromides give the corresponding naphthaflavones (ef. Nadkarni et. al., J., 1937,1798).
Item Type: | Article |
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Source: | Copyright of this article belongs to Royal Society of Chemistry. |
ID Code: | 80674 |
Deposited On: | 01 Feb 2012 09:55 |
Last Modified: | 01 Feb 2012 09:55 |
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