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Volume :23 Issue : 1 1996      Add To Cart                                                                    Download

Substituent effects on the photoaddition reactions of 1-naphthol to benzonitriles

Auther : NADER A. AL-JALAL

 Chemistry Department, Kuwait University, P.O. Box 5969, 13060 Safat (Kuwait)

 ABSTRACT

Methoxy-, methyl-, and chloro-substituted benzonitriles undergo photoaddition to 1-naphthol to give the substituted addition products, 5c - k, by initial attack of the cyano group on the aromatic ring of 1-naphthol. The efficiency of the photoaddition reaction varied with the position of the substituents, with the para-substituted benzonitriles giving the largest yield of photoproduct.

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