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

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作者：
AlJalal, NA
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来源：
JOURNAL OF THE UNIVERSITY OF KUWAIT-SCIENCE | 1996年 / 23卷 / 01期
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暂无
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O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号：
07 ; 0710 ; 09 ;
摘要：
Methoxy-, methyl-, and chloro-substituted benzonitriles undergo photoaddition to 1-naphthol to give the substituted addition products, 5(c-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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页码：39 / 46
页数：8
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