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

机译:香豆素的新型融合Furo,二氧和二氧衍生物的合成,光氧和DNA研究

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摘要

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 com-pounds (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.
机译:香豆素的新型融合Furo,二氧洛和二氧衍生物的合成是通过7,8-二羟基丙糖衍生物1与α-甲基苯甲甲基com-pouns(α-甲基甲酮,α-甲基酯,α-Haloesters和α-Haloetester和α-Haloacetyl and chlorooacetylyyl氯化物)的反应进行的。 二氯甲烷。 进行了合成的Furocoumarin衍生物的光氧化,并评估了Furocoumarin衍生物对DNA的亲和力,并将其与8-甲氧基索拉伦(8-mop)进行了比较,该(8-mop)在光化学治疗中广泛使用。

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