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- W1963855985 abstract "Osmometric and NMR techniques were used in order to study the ionic mechanism for the intramolecular photocycloaddition reaction of o-allyl phenols (1) to give cyclic ethers (2) + (3). The role of the intramolecular H-bond between the OH group and the π-electrons of the allylic group was ascertained. based on the results of the photocyclization, osmometric and NMR measurements the substituents can be divided into 3 groups according to their effect on the above intramolecular interaction." @default.
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- W1963855985 date "1975-01-01" @default.
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- W1963855985 title "On the mechanism of intramolecular photocycloaddition of substituted o-allylphenols to cyclic ethers" @default.
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- W1963855985 doi "https://doi.org/10.1016/0040-4020(75)80294-8" @default.
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