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2000
Volume 13, Issue 6
  • ISSN: 1570-1794
  • E-ISSN: 1875-6271

Abstract

A series of epoxyesters were lactonized by HClO4 to give corresponding -hydroxy-γ-lactones as a mixture of diastereoisomers: trans and cis. The mixtures of products were separated via column chromatography. The lactones synthesized were screened for anticancer activity against D17 and U2-OS cell lines. Only the trans isomer with naphthyl ring was found to exhibit significant activity against both cell lines.

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/content/journals/cos/10.2174/1570179413666151218201553
2016-12-01
2025-05-06
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