β-Aryl-ς-Hydroxy-γ-Lactones: Synthesis, Structural Analysis and Cytotoxic Activity

Author(s): Barbara Gawdzik , Alicja Wzorek , Angelika Kamizela , Mariusz Urbaniak , Witold Gladkowski , Magdalena Lis , Bozena Obminska-Mrukowicz , Agata Bialonska .

Journal Name: Current Organic Synthesis

Volume 13 , Issue 6 , 2016

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Abstract:

A series of epoxyesters were lactonized by HClO4 to give corresponding ς-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.

Keywords: Lactones, epoxyesters, aromatic ring, diastereoisomers, hydroxlactonization, antiproliferative activity.

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Article Details

VOLUME: 13
ISSUE: 6
Year: 2016
Page: [901 - 906]
Pages: 6
DOI: 10.2174/1570179413666151218201553
Price: $58

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