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- W2022764528 abstract "Photolysis of phenols 1a-d in chloroform or carbon tetrachloride afforded the corresponding di- or trichloromethyl phenyl ethers (2a-d or 6a-d, respectively). In chloroform, hydroxybenzaldehydes 4a-d or 5 and phenyl formates 3a-d were obtained as minor photoproducts. In carbon tetrachloride, traces of salicyloyl chloride (7), phenyl salicylate (8) and phenyl p-hydroxybenzoate (9) were detected starting from the parent phenol (1a). The obtained results agree with the involvement of an electron transfer mechanism." @default.
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- W2022764528 date "1995-05-01" @default.
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- W2022764528 title "Formation of dichloromethyl phenyl ethers as major products in the photo-Reimer-Tiemann reaction without base" @default.
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- W2022764528 doi "https://doi.org/10.1016/0040-4020(95)00235-z" @default.
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