Synthesis, Photooxygenation and DNA Studies of Novel Fused Furo, Dioxolo, and Dioxino Derivatives of Coumarin

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Abstract

Syntheses of novel fused furo, dioxolo and dioxino derivatives of coumarin are carried out through the reaction of 7,8-dihydroxycoumarin derivative 1 with α-halocarbonyl compounds (α-haloketone, α-haloester and chloroacetyl chloride) and 1,2-dichloroethane. The photooxygenation of synthesized furocoumarin derivative was performed and the affinity of furocoumarin derivative towards DNA was evaluated and compared with 8-methoxypsoralen (8-MOP), which extensively used in photochemotherapy.

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Elgogary, S. R. (2020). Synthesis, Photooxygenation and DNA Studies of Novel Fused Furo, Dioxolo, and Dioxino Derivatives of Coumarin. ChemistrySelect, 5(33), 10292–10297. https://doi.org/10.1002/slct.202002442

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