Summary
4-Isopropyl-1: 2-α-naphthapyrone is hydrolysed by dilute alkali to 1-hydroxy-2-naphthoic acid. It is further observed that 6-bromo- and 6-acetyl-4-isopropyl-1: 2-α-naphthapyrones are also hydrolysed to 4-bromo-and 4-acetyl-1-hydroxy-2-naphthoic acids. As the hydrolysis of the coumarins too-hydroxy carboxylic acids is unusual, these cases provide interesting exceptions to the usual behaviour.
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Ali, S.A., Desai, R.D. & Shroff, H.P. Heterocyclic compounds. Proc. Indian Acad. Sci. (Math. Sci.) 13, 184–187 (1941). https://doi.org/10.1007/BF03049264
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DOI: https://doi.org/10.1007/BF03049264