Journal
RUSSIAN CHEMICAL BULLETIN
Volume 72, Issue 9, Pages 2083-2089Publisher
SPRINGER
DOI: 10.1007/s11172-023-4002-z
Keywords
cobalt bis(dicarbollide); acridine; click-reaction; boron neutron capture therapy
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A new azidoethylaminoacridine compound was synthesized and boron-containing acridine conjugates were obtained through a specific reaction. These compounds have potential applications as DNA intercalators for boron neutron capture therapy.
A new 9-(azidoethylamino)acridine was obtained by the reaction of 9-methoxyacridine with N3CH2CH2NH2 & BULL; HCl by refluxing in MeCN. Boron-containing conjugates of acridine were synthesized by the CuI-catalyzed 1,3-dipolar [3+2] cycloaddition reaction of acetylene derivatives of cobalt bis(dicarbollide) with 9-azidoacridine. The complexes obtained can be used as boron-containing DNA intercalators for boron neutron capture therapy of cancer.
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