A number of new methylfurochromones with a linear psoralen-loke structure or an angular angelicin-like one were synthesized. The synthesis were performed starting from the appropriate 7-hydroxychromones on which the fura ring was built. Methyl groups were introduced into positions which look most promising for enhancement of the photoreactivity of the compound toward DNA.

Synthesis of some methylfurochromones as potential photochemotherapeutic agents.

CHILIN, ADRIANA;MANZINI, PAOLO;GUIOTTO, ADRIANO
1988

Abstract

A number of new methylfurochromones with a linear psoralen-loke structure or an angular angelicin-like one were synthesized. The synthesis were performed starting from the appropriate 7-hydroxychromones on which the fura ring was built. Methyl groups were introduced into positions which look most promising for enhancement of the photoreactivity of the compound toward DNA.
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/11577/2470773
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