Zhao Tian-tia
2015
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Journal
Chinese Journal of Synthetic Chemistry
Abstract
4-Carbonitrile-1-indanone in total yield of 32.1% was synthesized by a four-step reaction of condensation,alkaline hydrolysis,decarboxylation and Friedel-Crafts acylation reaction using 2-(chloromethyl) benzonitrile and diethyl malonate as the starting materials.The structure was confirmed by1 H NMR and13 C NMR.