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- W1999765235 abstract "New amino psoralen derivatives have been synthesized via bromination. Bromination of 3,5-substituted psoralens has been studied. The second position of the furan ring is more susceptible to bromination than the α-position of the chromen-2-one ring in psoralens. Hence, the target psoralenamines were synthesized starting with 3-bromo-7-hydroxy-4-methyl-chromen-2-one, which was condensed with different α-halo ketones and cyclized in ethanolic potassium hydroxide to get the desired 6-bromo psoralens, which were finally converted into psoralenamines. J. Heterocyclic Chem., (2010)." @default.
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- W1999765235 date "2010-01-01" @default.
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- W1999765235 title "Studies in synthesis of new psoralenamines" @default.
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- W1999765235 doi "https://doi.org/10.1002/jhet.327" @default.
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