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Synthesis 2011(19): 3173-3179
DOI: 10.1055/s-0030-1260157
DOI: 10.1055/s-0030-1260157
PAPER
© Georg Thieme Verlag
Stuttgart ˙ New York
Synthesis of a Novel Series of 1,2,3-Triazole-Containing Artemisinin Dimers with Potent Anticancer Activity Involving Huisgen 1,3-Dipolar Cycloaddition Reaction
Weitere Informationen
Received
12 May 2011
Publikationsdatum:
09. August 2011 (online)
Publikationsverlauf
Publikationsdatum:
09. August 2011 (online)

Abstract
A series of C-10 acetal triazolylartemisinin dimers were prepared via the Huisgen 1,3-dipolar cylcoaddition of artemisinin-derived terminal alkynes with 10α-azidoartemisinin and various aliphatic and aromatic diazides. All the artemisinin dimers synthesized exhibited strong growth inhibition activity against several cancer cell lines.
Key words
artemisinin - Artemisia annua - antimalarial - 1,2,3-triazole - artemisinin dimer
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